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A combinatorial method based on the determination of the averaged weight of permutations controlling the chirality/achirality fittingness of 2 <i> n </i> substitution sites of the monocyclic cycloalkane allows to obtain generalized functional equations for direct enumeration of enantiomers pairs and achiral skeletons of any derivatives of monocyclic cycloalkanes having heteromorphic alkyl substituents with the distinct length <i> k </i> with the empirical formula , wherein at least two alkyl groups of the distinct size each. is the number of alkyl radicals of the system verifying the relation . The integer sequences of enantiomer pairs and achiral skeletons are given for substituted derivatives of monocyclic cycloalkane for <i> n </i> = 3, 4 and <i> k </i> = 3, 4, 5. The composite stereoisomerism of this particular compound is also highlighted.

From the 1800s to 1870, the enumeration of isomers in chemistry consisted of a manual enumeration based on the so-called “draw and count” method which consists of drawing and counting all the possible molecular structures of a given organic compound in two dimensions or a plan. This exhausting exercise used to expose certain risks of repetition and/or omission of structures, especially for large molecules [

Chemists sorted out these difficulties of enumeration of chemical structures by developing methods and models of enumeration using not only mathematical theories (group theory, graph theory, etc.) but also more and more information technology tools (computers, softwares, etc.). This allowed to first generate several methods of enumeration of the isomers of constitution or function [

In this work, we are interested in determining the number of enantiomeric pairs and achiral skeletons of cycloalkanes with heteromorphic alkyl substituents of distinct order k. To simplify the language, we will speak of heteropolyalkylation of monocyclic cycloalkane with alkyl radicals of distinct k size. Beyond the direct formulas of computation established, this work highlights, on the one hand, a composite stereoisomerism due to the intrinsic chirality of the alkyl trees and to the extrinsic chirality induced by their positioning or placement on the monocycloalkane, on the other hand, the total number of different stereoisomers increases correlatively with the number of chiral centers present in the molecular graph and finally the concepts of pseudochirality, pseudosymmetry and enantiomeric mirror in the molecules of this family of saturated hydrocarbon compounds is also elucidated.

Let us consider the system C n H m 0 ( R k 1 ) m 1 ⋯ ( R k α ) m α ⋯ ( R k ζ ) m ζ , the empirical

formula of the heteropolyalkylated monocyclic cycloalkane having heteromorphous alkyl substituents including at least two alkyl groups noted R k α = C k α H 2 k α + 1 , having the distinct order, size or length k α , with ( 1 ≤ α ≤ ζ ). m α is the number

of alkyl radicals R k α of the system C n H m 0 ( R k 1 ) m 1 ⋯ ( R k α ) m α ⋯ ( R k ζ ) m ζ where ∑ α = 1 ζ m α + m 0 = 2 n .

The molecular composite stereograph G k α of the system

C n H m 0 ( R k 1 ) m 1 ⋯ ( R k α ) m α ⋯ ( R k ζ ) m ζ

is obtained by connecting the roots of the graphs of the distinct planted steric trees R k α to the sites or positions of substitution of the stereograph G of the parent molecule of the monocyclic cycloalkane C n H 2 n described in our previous work [

G k α = G ∘ R k α ( 1 ≤ α ≤ ζ ) = C n H m 0 ( R k 1 ) m 1 ⋯ ( R k α ) m α ⋯ ( R k ζ ) m ζ (1)

G k α is the stereograph of a monocyclic cycloalkane heteropolyalkylated having alkyl radicals R k α of distinct size k. The approach used to enumerate stereoisomers of the system C n H m 0 ( R k 1 ) m 1 ⋯ ( R k α ) m α ⋯ ( R k ζ ) m ζ is to first determine

the number of heteromorphic combinations of distinct alkyl radicals of orders k α , with ( 1 ≤ α ≤ ζ ), and then to carry out the product of the latter by the results of the enumeration of the stereoisomers of the homopolysubstituted and/or heteropolysubstituted monocyclic cycloalkane obtained in our previous work [

According to graph theory, any alkyl radical C k H 2 k + 1 is equivalent to a planted steric tree which may have one or more isomers or stereoisomers including the chiral and achiral forms. s_{k} and p_{k} respectively give the total number and the number of steric trees planted of order k. We recall that the generating functions which give these numbers were established by Robinson et al. [

series: s ( x ) = ∑ k s k x k and p ( x ) = ∑ k p k x k for 0 ≤ k ≤ 14 . Values of s_{k}, p_{k}_{ }and s_{k}-p_{k} for 0 ≤ k ≤ 18 are computed and compiled in

Graphs of planted steric trees ( C k H 2 k + 1 ) can be combined in three sets whose

k | s_{k} | p_{k} | s_{k}-p_{k} |
---|---|---|---|

0 | 1 | 1 | 0 |

1 | 1 | 1 | 0 |

2 | 1 | 1 | 0 |

3 | 2 | 2 | 0 |

4 | 5 | 3 | 2 |

5 | 11 | 5 | 6 |

6 | 28 | 8 | 20 |

7 | 74 | 14 | 60 |

8 | 199 | 23 | 176 |

9 | 551 | 41 | 510 |

10 | 1533 | 69 | 1464 |

11 | 4436 | 122 | 4314 |

12 | 12,832 | 208 | 12,624 |

13 | 37,496 | 370 | 37,126 |

14 | 110,500 | 636 | 109,864 |

15 | 327,420 | 1134 | 326,286 |

16 | 979,819 | 1963 | 977,856 |

17 | 2,944,873 | 3505 | 2,941,368 |

18 | 8,896,515 | 6099 | 8,890,416 |

elements are equivalent to stereoisomers of sterically distinct alkyl radicals, namely:

- E_{a}_{+c} is the set of chiral and achiral trees of cardinality s_{k}. Elements of E_{a}_{+c} are pairs of enantiomers and achiral skeletons.

- E_{a} is the set of achiral trees of cardinality p_{k}. Elements of E_{a} are achiral skeletons.

- E_{c} is the set pairs enantiomers of cardinality s_{k}-p_{k}.

From these definitions, we can write the following relations:

| E c + a | = s k , | E a | = p k ⇒ { E c + a = E c ∪ E a E c ∩ E a = ϕ (2)

Considering (2), we have:

| E c + a | = | E c | + | E a | ⇒ | E c | = | E c + a | − | E a | (3)

And consequently | E c | = s k − p k (4)

Note that a pair of enantiomers is represented by the same letter whose two stereoisomers are differentiated by the apostrophe.

Size k | Alkyl radicals or planted trees |
---|---|

1 | |

2 | |

3 | |

4 | |

5 |

Before calculating the numbers of heteromorphic combinations of distinct alkyl radicals of different order k, we first define the different sets of alkyl radicals of distinct orders k α , with ( 1 ≤ α ≤ ζ ). I R k α is a set constituted of chiral and achiral alkyl radicals having k α carbons. Considering

I R k 1 = I R 1 = { A 1 }

I R k 2 = I R 2 = { A 2 }

I R k 3 = I R 3 = { A 3 , B 3 }

I R k 4 = I R 4 = { A 4 , B 4 , C 4 , D 4 , D ′ 4 }

I R k 5 = I R 5 = { A 5 , B 5 , C 5 , D 5 , E 5 , E ′ 5 , F , F ′ 5 , G , G ′ 5 }

We can generalize all these sets as follows:

I R k α = { A α , B α , C α , D α , D ′ α , ⋯ , Z α , Z ′ α } .

- I R k α a designates a set formed of alkyl radicals only achiral and having the same order k α .

Example: I R 1 a = { A 1 } , I R 2 a = { A 2 } , I R 3 a = { A 3 , B 3 } , I R 4 a = { A 4 , B 4 , C 4 } , I R 5 a = { A 5 , B 5 , C 5 , D 5 , E 5 } , ⋯

- I R k α c means a group consisting of only chiral alkyl radicals and having the same order k α .

Example: I R 4 c = { D 5 , D ′ 5 } , I R 5 c = { F 5 , F ′ 5 , G 5 , G ′ 5 , H 5 , H ′ 5 } , ⋯

- C a r d I R k α = s k α , C a r d I R k α a = p k α and C a r d I R k α c = s k α − p k α .

- A group of substituents or alkyl radicals refers in this chapter to a combination of at least two different substituent types selected from at least two sets of alkyl radicals of order k α different and that composes a substitution.

Example: Heteromorphous substituent groups A_{1}A_{3} and A_{1}B_{3} were formed by combining a radical of I R 1 a and one of I R 3 a .

- i is the number of substituent types or alkyl radicals that make up a group of substituents or else i-uples. i α is the number of substituent or alkyl radical of order k α chosen in I R k α , I R k α a or I R k α c such that i α ≤ s k α , p k α or s k α − p k α and ∑ α i α = i .

Example: In the group of heteromorphic substituents A_{1}A_{3}B_{3}, i_{3} = 2, i_{1} = 1 and i = 3; in heteromorphous substituent groups A_{1}A_{3} and A_{1}B_{3} we have i_{3} = 1, i_{1} = 1 and i = 2.

Following these definitions, we can roll out the algorithm of our method of counting the stereoisomers of the molecular system

C n H m 0 ( R k 1 ) m 1 ⋯ ( R k α ) m α ⋯ ( R k ζ ) m ζ

as follows by first establishing the formula for calculating the number of substituting group or number of i-uples of letters identifying the alkyl radicals.

The number of i-uples of distinct letters without repetition or groups of substituents taken in I R k α , I R k α a or I R k α c ( 1 ≤ α ≤ ζ ) in such a way that we have i types of heteromorphic substituents of different orders k α and composing a substitution is given respectively by N k 1 , k 2 , ⋯ , k α = ∏ α ( s k α i α ) , N k 1 , k 2 , ⋯ , k α a = ∏ α ( p k α i α ) and N k 1 , k 2 , ⋯ , k α c = ∏ α ( s k α − p k α i α ) .

The number of i-tuples mixed letter representing heteromorphic combinations of chiral and achiral radicals of distinct orders is given by

N k 1 , k 2 , ⋯ , k α a + c = N k 1 , k 2 , ⋯ , k α − N k 1 , k 2 , ⋯ , k α a − N k 1 , k 2 , ⋯ , k α c .

Example:

1) Let us determine the number of substituent groups having 2 types of substituents or even 2-ones of letters of which one is taken in I R 3 and in I R 4 .

We have I R 3 = { A 3 , B 3 } , I R 4 = { A 4 , B 4 , C 4 , D 4 , D ′ 4 } , s 4 = 5 , p 4 = 3 , s 4 − p 4 = 2 , i 4 = 1 , s 3 = 2 , p 3 = 2 , s 3 − p 3 = 0 , i 3 = 1 then

N 3 , 4 = ( 2 1 ) ⋅ ( 5 1 ) = 10

which corresponds to the groups of substituents A_{3}A_{4}, A_{3}B_{4}, A_{3}C_{4}, A_{3}D_{4}, A 3 D ′ 4 ,

B_{3}A_{4}, B_{3}B_{4}, B_{3}C_{4}, B_{3}D_{4}, B 3 D ′ 4 , N 3 , 4 c = 0 , N 3 , 4 a = ( 2 1 ) ⋅ ( 3 1 ) = 6 which corresponds

to the groups of substituents A_{3}A_{4}, A_{3}B_{4}, A_{3}C_{4}, B_{3}A_{4}, B_{3}B_{4}, B_{3}C_{4}. N 3 , 4 a + c = 10 − 6 = 4 which corresponds to the group of substituents A_{3}D_{4}, A 3 D ′ 4 , B_{3}D_{4}, B 3 D ′ 4 .

2) Let us determine the number of substituent groups having 4 substituent types or even 4-tuples of letters of which one is chosen from I R 1 , one in I R 2 and 2 in I R 3 .

We have I R 1 = { A 1 } , I R 2 = { A 2 } and I R 3 = { A 3 , B 3 } ; s 1 = 1 , p 1 = 1 , s 1 − p 1 = 0 , i 1 = 1 , s 2 = 1 , p 2 = 1 , s 2 − p 2 = 0 , i 2 = 1 , s 3 = 2 , p 3 = 2 , s 3 − p 3 = 0 , i 3 = 2 ; N 1 , 2 , 3 = N 1 , 2 , 3 a = ( 1 1 ) ⋅ ( 1 1 ) ⋅ ( 2 2 ) = 1 which is the group de substituents A_{1}A_{2}A_{3}B_{3}, N 1 , 2 , 3 c = 0 , N 1 , 2 , 3 a + c = 0 .

3) Let us determine the number of substituent groups having 6 substituent types or even 6-tuples of letters, one of which is chosen from I R 1 , one in I R 2 , two in I R 3 and two in I R 4 .

We have I R 1 = { A 1 } , I R 2 = { A 2 } , I R 3 = { A 3 , B 3 } and

I R 4 = { A 4 , B 4 , C 4 , D 4 , D ′ 4 } ;

s 1 = 1 , p 1 = 1 , s 1 − p 1 = 0 , i 1 = 1 , s 2 = 1 , p 2 = 1 , s 2 − p 2 = 0 , i 2 = 1 , s 3 = 2 , p 3 = 2 , s 3 − p 3 = 0 , i 3 = 1 , s 4 = 5 , p 4 = 3 , s 4 − p 4 = 2 , i 4 = 2

We obtain N 1 , 2 , 3 , 4 = ( 1 1 ) ⋅ ( 1 1 ) ⋅ ( 2 2 ) ⋅ ( 5 2 ) = 10 which is the following groups of

substituents: A_{1}A_{2}A_{3}B_{3}A_{4}B_{4}, A_{1}A_{2}A_{3}B_{3}A_{4}C_{4}, A_{1}A_{2}A_{3}B_{3}A_{4}D_{4}, A 1 A 2 A 3 B 3 A 4 D ′ 4 , A_{1}A_{2}A_{3}B_{3}B_{4}C_{4}, A_{1}A_{2}A_{3}B_{3}B_{4}D_{4}, A 1 A 2 A 3 B 3 B 4 D ′ 4 , A_{1}A_{2}A_{3}B_{3}C_{4}D_{4}, A 1 A 2 A 3 B 3 C 4 D ′ 4 ,

A 1 A 2 A 3 B 3 D 4 D ′ 4 ; N 1 , 2 , 3 , 4 a = ( 1 1 ) ⋅ ( 1 1 ) ⋅ ( 2 2 ) ⋅ ( 3 2 ) = 3 is the groups of substituents:

A_{1}A_{2}A_{3}B_{3}A_{4}B_{4}, A_{1}A_{2}A_{3}B_{3}A_{4}C_{4}, A_{1}A_{2}A_{3}B_{3}B_{4}C_{4}; N 1 , 2 , 3 , 4 c = 0 ; N 1 , 2 , 3 , 4 a + c = 10 − 3 = 7 which corresponds to the following groups of substituents: A_{1}A_{2}A_{3}B_{3}A_{4}D_{4}, A 1 A 2 A 3 B 3 A 4 D ′ 4 , A_{1}A_{2}A_{3}B_{3}B_{4}D_{4}, A 1 A 2 A 3 B 3 B 4 D ′ 4 , A_{1}A_{2}A_{3}B_{3}C_{4}D_{4}, A 1 A 2 A 3 B 3 C 4 D ′ 4 , A 1 A 2 A 3 B 3 D 4 D ′ 4 .

The “stereoisomeric” composition of the system

C n H m 0 ( R k 1 ) m 1 ⋯ ( R k α ) m α ⋯ ( R k ζ ) m ζ

results from 1) the nature of alkyl radicals of distinct k-size (chiral or achiral tree) and 2) the manner of attaching or implanting them to the monocycle (chiral or achiral location on the monocycle).

Unlike the polyalkylation of the monocyclic cycloalkane treated by Nemba et al. [

The composite stereoisomerism resulting from the present exercise of heteropolyalkylation of the monocyclic cycloalkane is summarized in

The different entities of

A c c ( n ; m 0 , m 1 , ⋯ , m α , ⋯ , m ζ ; k 1 , ⋯ , k α , ⋯ , k ζ ) : is the number of chiral stereoisomers composed from chiral alkyls (Chiral Radicals—Chiral Placements);

A a c ( n ; m 0 , m 1 , ⋯ , m α , ⋯ , m ζ ; k 1 , ⋯ , k α , ⋯ , k ζ ) : is the number of achiral stereoisomers compounded from chiral alkyls (Chiral Radicals—Achiral Placements);

Chirality or achirality of the heteropolyalkylated monocycloalkane | Combinations of steric configurations of alkyl radicals | ||
---|---|---|---|

Characteristics of placements m_{1}, …, m_{g}, …, m_{sk} alkyl trees | All the radicals combined i to i are chiral | All the radicals combined i to i are achiral | All the radicals combined i to i are achiral and chiral |

Chiral placements | Chiral radicals—Chiral placement ( A c c ) | Achiral radicals—Chiral placement ( A c a ) | Achiral and chiral radicals—Chiral placement ( A c a + c ) |

Achiral placements | Chiral radicals—Achiral placement ( A a c ) | Achiral radicals—Achiral placement ( A a a ) | Achiral and chiral radicals—Achiral placement ( A a a + c ) |

A c a ( n ; m 0 , m 1 , ⋯ , m α , ⋯ , m ζ ; k 1 , ⋯ , k α , ⋯ , k ζ ) : is the number of chiral stereoisomers composed of achiral alkyl trees (Achiral Radicals—Chiral Placements);

A a a ( n ; m 0 , m 1 , ⋯ , m α , ⋯ , m ζ ; k 1 , ⋯ , k α , ⋯ , k ζ ) : is the number of achiral stereoisomers compounded from achiral alkyl trees (Achiral Radicals—Achiral Placements);

A c a − c ( n ; m 0 , m 1 , ⋯ , m α , ⋯ , m ζ ; k 1 , ⋯ , k α , ⋯ , k ζ ) : is the number of chiral stereoisomers composed of achiral and chiral alkyl trees (Achiral and chiral radicals—chiral Placements);

A a a − c ( n ; m 0 , m 1 , ⋯ , m α , ⋯ , m ζ ; k 1 , ⋯ , k α , ⋯ , k ζ ) : is the number of achiral stereoisomers composed of achiral and chiral alkyl trees (Achiral and chiral radicals—Achiral Placements).

The number of chiral and achiral stereoisomers of a monocyclic cycloalkane heteropolysubstituted by alkyl groups of distinct orders k is directly obtained from the product of the number of groups of substituents N k 1 , k 2 , ⋯ , k α c , N k 1 , k 2 , ⋯ , k α a , N k 1 , k 2 , ⋯ , k α a + c by the number of chiral placements A c ( n , m 0 , m 1 , ⋯ , m α , ⋯ , m ζ ) and achiral placements A a ( n , m 0 , m 1 , ⋯ , m α , ⋯ , m ζ ) of alkyl trees on the monocyclic cycloalkane of size n.

For this purpose, we recall the results of our recurrence formulas established in previous papers [

A c c ( n ; m 0 , m 1 , ⋯ , m α , ⋯ , m ζ ; k 1 , ⋯ , k α , ⋯ , k ζ ) = N k 1 , k 2 , ⋯ , k α c × A c ( n , m 0 , m 1 , ⋯ , m α , ⋯ , m ζ ) (5)

A a c ( n ; m 0 , m 1 , ⋯ , m α , ⋯ , m ζ ; k 1 , ⋯ , k α , ⋯ , k ζ ) = N k 1 , k 2 , ⋯ , k α c × A a ( n , m 0 , m 1 , ⋯ , m α , ⋯ , m ζ ) (6)

A c a ( n ; m 0 , m 1 , ⋯ , m α , ⋯ , m ζ ; k 1 , ⋯ , k α , ⋯ , k ζ ) = N k 1 , k 2 , ⋯ , k α a × A c ( n , m 0 , m 1 , ⋯ , m α , ⋯ , m ζ ) (7)

A a a ( n ; m 0 , m 1 , ⋯ , m α , ⋯ , m ζ ; k 1 , ⋯ , k α , ⋯ , k ζ ) = N k 1 , k 2 , ⋯ , k α a × A a ( n , m 0 , m 1 , ⋯ , m α , ⋯ , m ζ ) (8)

A c a + c ( n ; m 0 , m 1 , ⋯ , m α , ⋯ , m ζ ; k 1 , ⋯ , k α , ⋯ , k ζ ) = N k 1 , k 2 , ⋯ , k α a + c × A c ( n , m 0 , m 1 , ⋯ , m α , ⋯ , m ζ ) (9)

A a a + c ( n ; m 0 , m 1 , ⋯ , m α , ⋯ , m ζ ; k 1 , ⋯ , k α , ⋯ , k ζ ) = N k 1 , k 2 , ⋯ , k α a + c × A a ( n , m 0 , m 1 , ⋯ , m α , ⋯ , m ζ ) (10)

Therefore, the total number of chiral skeletons of the system

C n H m 0 ( R k 1 ) m 1 ⋯ ( R k α ) m α ⋯ ( R k ζ ) m ζ

is given by:

A c k 1 , ⋯ , k α , ⋯ , k ζ ( n ; m 0 , m 1 , ⋯ , m α , ⋯ , m ζ ; k 1 , ⋯ , k α , ⋯ , k ζ ) = A c c ( n ; m 0 , m 1 , ⋯ , m α , ⋯ , m ζ ; k 1 , ⋯ , k α , ⋯ , k ζ ) + A a c ( n ; m 0 , m 1 , ⋯ , m α , ⋯ , m ζ ; k 1 , ⋯ , k α , ⋯ , k ζ ) + A c a ( n ; m 0 , m 1 , ⋯ , m α , ⋯ , m ζ ; k 1 , ⋯ , k α , ⋯ , k ζ ) + A c a + c ( n ; m 0 , m 1 , ⋯ , m α , ⋯ , m ζ ; k 1 , ⋯ , k α , ⋯ , k ζ ) + A a a + c ( n ; m 0 , m 1 , ⋯ , m α , ⋯ , m ζ ; k 1 , ⋯ , k α , ⋯ , k ζ ) (11)

And the total number of achiral stereoisomers is:

A a k 1 , ⋯ , k α , ⋯ , k ζ ( n ; m 0 , m 1 , ⋯ , m α , ⋯ , m ζ ; k 1 , ⋯ , k α , ⋯ , k ζ ) = A a a ( n ; m 0 , m 1 , ⋯ , m α , ⋯ , m ζ ; k 1 , ⋯ , k α , ⋯ , k ζ ) (12)

We have I R 1 = { A 1 } , I R 2 = { A 2 } ; s 1 = 1 , p 1 = 1 , s 1 − p 1 = 0 , i 1 = 1 , s 2 = 1 ,

p 2 = 1 , s 2 − p 2 = 0 , i 2 = 1 ; N 1 , 2 = N 1 , 2 a = ( 1 1 ) ⋅ ( 1 1 ) = 1 which corresponds to the group of substituents A_{1}A_{2}, N 1 , 2 c = 0 , N 1 , 2 a + c = 0 .

The group of substituents A_{1}A_{2} induces heteropolyalkylation of type C 3 H m 0 X m 1 Y m 2 where X = A 1 , Y = A 2 or X = A 2 and Y = A 1 and m 0 + m 1 + m 2 = 6 . The numbers of stereoisomers A a a , A c a , A a c , A c c , A a a + c and A c a + c are respectively obtained from the following formulas:

A a a = N 1 , 2 a × A a , A c a = N 1 , 2 a × A c , A a c = N 1 , 2 c × A a , A c c = N 1 , 2 c × A c , A a a + c = N 1 , 2 a + c × A a and A c a + c = N 1 , 2 a + c × A c .

The numbers of stereoisomers corresponding to placements or positions A a and A c of C 3 H m 0 X m 1 Y m 2 having m 0 ≠ 0 , m 1 ≠ 0 , m 2 ≠ 0 are the same with those of the system C n X m 1 Y m 2 Z m 3 which have been calculated in our previous paper for n = 3 [

The numbers of stereoisomers corresponding to placements or positions A a and A c of C 3 H m 0 X m 1 Y m 2 having m 0 = 0 , m 1 ≠ 0 , m 2 ≠ 0 are equivalent to those of the system C n H 2 n − m X m given in our previous paper for n = 3 [

Using all these data, the inventory of stereoisomers of the heteropolyalkylated cyclopropane having two distinct alkyl trees methyl ( i 1 = 1 ) and ethyl ( i 2 = 1 ) is summarized in

m_{0} | m_{1} | m_{2} | A a | A c | A a a | A c a | A a c | A c c | A a a + c | A c a + c |
---|---|---|---|---|---|---|---|---|---|---|

1 | 1 | 4 | 1 | 2 | 1 | 2 | 0 | 0 | 0 | 0 |

1 | 2 | 3 | 2 | 4 | 2 | 4 | 0 | 0 | 0 | |

2 | 2 | 2 | 4 | 7 | 4 | 7 | 0 | 0 | 0 | 0 |

0 | 1 | 5 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | 0 |

0 | 2 | 4 | 2 | 1 | 2 | 1 | 0 | 0 | 0 | 0 |

0 | 3 | 3 | 2 | 1 | 2 | 1 | 0 | 0 | 0 | 0 |

Some graphical representations:

n = 3, m_{0} = 4, m_{1} = 1, m_{2} = 1:

n = 3, m_{0} = 3, m_{1} = 2, m_{2} = 1:

We have I R 1 = { A 1 } , I R 2 = { A 2 } ; s 1 = 1 , p 1 = 1 , s 1 − p 1 = 0 , i 1 = 1 , s 2 = 1 ,

p 2 = 1 , s 2 − p 2 = 0 , i 2 = 1 ; N 1 , 2 = N 1 , 2 a = ( 1 1 ) ⋅ ( 1 1 ) = 1 which corresponds to the group of substituents A_{1}A_{2}, N 1 , 2 c = 0 , N 1 , 2 a + c = 0 .

The group of substituents A_{1}A_{2} induces heteropolyalkylation of type C 4 H m 0 X m 1 Y m 2 with X = A 1 , Y = A 2 or X = A 2 , Y = A 1 and m 0 + m 1 + m 2 = 8 . The numbers of stereoisomers A a a A c a , A a c , A c c , A a a + c and A c a + c are respectively obtained from the following formulas:

A a a = N 1 , 2 a × A a , A c a = N 1 , 2 a × A c , A a c = N 1 , 2 c × A a , A c c = N 1 , 2 c × A c , A a a + c = N 1 , 2 a + c × A a and A c a + c = N 1 , 2 a + c × A c .

The numbers of stereoisomers corresponding to placements or positions A a and A c of C 4 H m 0 X m 1 Y m 2 having m 0 ≠ 0 , m 1 ≠ 0 , m 2 ≠ 0 are the same with those of the system C n X m 1 Y m 2 Z m 3 which have been calculated in our previous paper for n = 4 [

The numbers of stereoisomers corresponding to placements or positions A a and A c of C 4 H m 0 X m 1 Y m 2 having m 0 = 0 , m 1 ≠ 0 , m 2 ≠ 0 are equivalent to those of the system C n H 2 n − m X m given in our previous paper for n = 4 [

Using all these data, the inventory of stereoisomers of the heteropolyalkylated cyclobutane having two distinct alkyl trees methyl ( i 1 = 1 ) and ethyl ( i 2 = 1 ) is summarized in

Representation of some graphs:

n = 4, m_{0} = 5, m_{1} = 2, m_{2} = 1:

We have I R 3 = { A 3 , B 3 } , I R 4 = { A 4 , B 4 , C 4 , D 4 , D ′ 4 } , s 4 = 5 , p 4 = 3 , s 4 − p 4 = 2 , i 4 = 1 , s 3 = 2 , p 3 = 2 , s 3 − p 3 = 0 , i 3 = 1 then N 3 , 4 = ( 2 1 ) ⋅ ( 5 1 ) = 10 which corresponds to groups of substituents A_{3}A_{4}, A_{3}B_{4}, A_{3}C_{4}, A_{3}D_{4}, A 3 D ′ 4 , B_{3}A_{4}, B_{3}B_{4}, B_{3}C_{4}, B_{3}D_{4}, B 3 D ′ 4 , N 3 , 4 c = 0 , N 3 , 4 a = ( 2 1 ) ⋅ ( 3 1 ) = 6 which corresponds to the groups of substituents A_{3}A_{4}, A_{3}B_{4}, A_{3}C_{4}, B_{3}A_{4}, B_{3}B_{4}, B_{3}C_{4} ; N 3 , 4 a + c = 10 − 6 = 4 which corresponds to the group of substituents A_{3}D_{4}, A 3 D ′ 4 , B_{3}D_{4}, B 3 D ′ 4 .

All groups of substituents give heteropolyalkylations of type C 3 H m 0 X m 1 Y m 2 such as m 0 + m 1 + m 2 = 6 ; with the group de substituents A_{3}B_{4} for example, we can make the assignment X = A 3 , Y = B 4 or X = B 4 , Y = A 3 . Numbers of stereoisomers A a a , A c a , A a c , A c c , A a a + c and A c a + c are respectively obtained from the following formulas:

m_{0} | m_{1} | m_{2} | A a | A a a | A c a | A a c | A c c | A a a + c | A c a + c | |
---|---|---|---|---|---|---|---|---|---|---|

6 | 1 | 1 | 3 | 2 | 3 | 2 | 0 | 0 | 0 | 0 |

5 | 2 | 1 | 5 | 8 | 5 | 8 | 0 | 0 | 0 | |

4 | 2 | 2 | 14 | 23 | 14 | 23 | 0 | 0 | 0 | 0 |

4 | 3 | 1 | 7 | 14 | 7 | 14 | 0 | 0 | 0 | 0 |

3 | 3 | 2 | 10 | 30 | 10 | 30 | 0 | 0 | 0 | 0 |

2 | 3 | 3 | 10 | 30 | 10 | 30 | 0 | 0 | 0 | 0 |

0 | 7 | 1 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | 0 |

0 | 6 | 2 | 4 | 1 | 4 | 1 | 0 | 0 | 0 | 0 |

0 | 5 | 3 | 3 | 2 | 3 | 2 | 0 | 0 | 0 | 0 |

0 | 4 | 4 | 7 | 3 | 7 | 3 | 0 | 0 | 0 | 0 |

A a a = N 4 a × A a , A c a = N 4 a × A c , A a c = N 4 c × A a , A c c = N 4 c × A c , A a a + c = N 4 a + c × A a and A c a + c = N 4 a + c × A c with N 3 , 4 a = 6 , N 3 , 4 c = 0 and N 3 , 4 a + c = 4 .

The numbers of stereoisomers corresponding to placements or positions A a and A c of C 3 H m 0 X m 1 Y m 2 having m 0 ≠ 0 , m 1 ≠ 0 , m 2 ≠ 0 are the same with those of the system C n X m 1 Y m 2 Z m 3 which have been calculated in our previous paper for n = 3 [

The numbers of stereoisomers corresponding to placements or positions A a and A c of C 3 H m 0 X m 1 Y m 2 having m 0 = 0 , m 1 ≠ 0 , m 2 ≠ 0 are equivalent to those of the system C n H 2 n − m X m given in our previous paper for n = 3 [

Using all these data, the inventory of stereoisomers of the heteropolyalkylated cyclopropane having two heteromorphous radicals propyl ( i 3 = 1 ) and butyl ( i 4 = 1 ) is summarized in

Some graphical representations:

n = 3, m_{0} = 4, m_{1} = 1, m_{2} = 1:

m_{0} | m_{1} | m_{2} | A a | A c | A a a | A c a | A a c | A c c | A a a + c | A c a + c |
---|---|---|---|---|---|---|---|---|---|---|

1 | 1 | 4 | 1 | 2 | 6 | 36 | 0 | 0 | 4 | 8 |

1 | 2 | 3 | 2 | 4 | 12 | 24 | 0 | 0 | 8 | 16 |

2 | 2 | 2 | 4 | 7 | 24 | 42 | 0 | 0 | 16 | 28 |

0 | 1 | 5 | 1 | 0 | 6 | 0 | 0 | 0 | 4 | 0 |

0 | 2 | 4 | 2 | 1 | 12 | 6 | 0 | 0 | 8 | 4 |

0 | 3 | 3 | 2 | 1 | 12 | 6 | 0 | 0 | 8 | 4 |

We have I R 3 = { A 3 , B 3 } , I R 4 = { A 4 , B 4 , C 4 , D 4 , D ′ 4 } , s 4 = 5 , p 4 = 3 , s 4 − p 4 = 2 , i 4 = 1 , s 3 = 2 , p 3 = 2 , s 3 − p 3 = 0 , i 3 = 1 then N 3 , 4 = ( 2 1 ) ⋅ ( 5 1 ) = 10 which corresponds to groups of substituents A_{3}A_{4}, A_{3}B_{4}, A_{3}C_{4}, A_{3}D_{4}, A 3 D ′ 4 , B_{3}A_{4}, B_{3}B_{4}, B_{3}C_{4}, B_{3}D_{4}, B 3 D ′ 4 , N 3 , 4 c = 0 , N 3 , 4 a = ( 2 1 ) ⋅ ( 3 1 ) = 6 which corresponds to the group of substituents A_{3}A_{4}, A_{3}B_{4}, A_{3}C_{4}, B_{3}A_{4}, B_{3}B_{4}, B_{3}C_{4}. N 3 , 4 a + c = 10 − 6 = 4 which corresponds to groups of substituents A_{3}D_{4}, A 3 D ′ 4 , B_{3}D_{4}, B 3 D ′ 4 .

The groups of substituents induce heteropolyalkylation of type C 4 H m 0 X m 1 Y m 2 such as m 0 + m 1 + m 2 = 8 , with the group de substituents A_{3}B_{4} for example, we can make the assignment X = A 3 , Y = B 4 or X = B 4 , Y = A 3 .

The numbers of stereoisomers A a a , A c a , A a c , A c c , A a a + c and A c a + c are respectively obtained from the following formulas:

A a a = N 3 , 4 a × A a , A c a = N 3 , 4 a × A c , A a c = N 3 , 4 c × A a , A c c = N 3 , 4 c × A c , A a a + c = N 3 , 4 a + c × A a and A c a + c = N 3 , 4 a + c × A c , with N 3 , 4 a = 6 , N 3 , 4 c = 0 and N 3 , 4 a + c = 4 .

The numbers of stereoisomers corresponding to placements or positions A a and A c of C 4 H m 0 X m 1 Y m 2 having m 0 ≠ 0 , m 1 ≠ 0 , m 2 ≠ 0 are the same with those of the system C n X m 1 Y m 2 Z m 3 which have been calculated in our previous paper for n = 4 [

The numbers of stereoisomers corresponding to placements or positions A a and A c of C 4 H m 0 X m 1 Y m 2 having m 0 = 0 , m 1 ≠ 0 , m 2 ≠ 0 are equivalent to those of the system C n H 2 n − m X m given in our previous paper for n = 4 [

Using all these data, the inventory of stereoisomers of the heteropolyalkylated cyclobutane having two heteromorphous radicals propyl ( i 3 = 1 ) and butyl ( i 4 = 1 ) is summarized in

m_{0} | m_{1} | m_{2} | A a | A c | A a a | A c a | A a c | A c c | A a a + c | A c a + c |
---|---|---|---|---|---|---|---|---|---|---|

6 | 1 | 1 | 3 | 2 | 18 | 12 | 0 | 0 | 12 | 8 |

5 | 2 | 1 | 5 | 8 | 30 | 48 | 0 | 0 | 20 | 32 |

4 | 2 | 2 | 14 | 23 | 84 | 138 | 0 | 0 | 56 | 92 |

4 | 3 | 1 | 7 | 14 | 42 | 84 | 0 | 0 | 28 | 56 |

3 | 3 | 2 | 10 | 30 | 60 | 180 | 0 | 0 | 40 | 120 |

0 | 7 | 1 | 1 | 0 | 6 | 0 | 0 | 0 | 4 | 0 |

0 | 6 | 2 | 4 | 1 | 24 | 6 | 0 | 0 | 16 | 4 |

0 | 5 | 3 | 3 | 2 | 18 | 12 | 0 | 0 | 12 | 8 |

0 | 4 | 4 | 7 | 3 | 42 | 18 | 0 | 0 | 28 | 12 |

Some graphical representations:

n = 4, m_{0} = 6, m_{1} = 1, m_{2} = 1:

We have I R 3 = { A 3 , B 3 } , I R 4 = { A 4 , B 4 , C 4 , D 4 , D ′ 4 } , s 4 = 5 , p 4 = 3 , s 4 − p 4 = 2 , i 4 = 1 , s 3 = 2 , p 3 = 2 , s 3 − p 3 = 0 , i 3 = 2 then N 3 , 4 = ( 2 2 ) ⋅ ( 5 1 ) = 5 which corresponds to groups of substituents A_{3}B_{3}A_{4}, A_{3}B_{3}B_{4}, A_{3}B_{3}C_{4}, A_{3}B_{3}D_{4}, A 3 B 3 D ′ 4 ; N 3 , 4 c = 0 , N 3 , 4 a = ( 2 2 ) ⋅ ( 3 1 ) = 3 which corresponds to groups of substituents A_{3}B_{3}A_{4}, A_{3}B_{3}B_{4}, A_{3}B_{3}C_{4}; N 3 , 4 a + c = 5 − 3 = 2 which corresponds to groups of substituents A_{3}B_{3}D_{4}, A 3 B 3 D ′ 4 .

All those groups of substituents generate heteropolyalkylations of type C 3 H m 0 X m 1 Y m 2 Z m 3 such as m 0 + m 1 + m 2 + m 3 = 6 ; with the group of substituents A_{3}B_{3}C_{4} for example, we can make the assignment X = A 3 , Y = B 3 , Z = C 4 ; X = A 3 , Y = C 4 , Z = B 3 ; X = B 3 , Y = A 3 , Z = C 4 ; X = B 3 , Y = C 4 , Z = A 3 ; X = C 4 , Y = A 3 , Z = B 3 ; X = C 4 , Y = B 3 , Z = A 3 . The numbers of stereoisomers A a a , A c a , A a c , A c c , A a a + c and A c a + c are respectively obtained from the following formulas:

A a a = N 3 , 4 a × A a , A c a = N 3 , 4 a × A c , A a c = N 3 , 4 c × A a , A c c = N 3 , 4 c × A c , A a a + c = N 3 , 4 a + c × A a and A c a + c = N 3 , 4 a + c × A c , with N 3 , 4 a = 3 , N 3 , 4 c = 0 and N 3 , 4 a + c = 2 .

The numbers of stereoisomers corresponding to placements or positions A a and A c of C 3 H m 0 X m 1 Y m 2 Z m 3 having m 0 ≠ 0 , m 1 ≠ 0 , m 2 ≠ 0 , m 3 ≠ 0 are the same with those of the system C n X m 1 Y m 2 Z m 3 U m 4 which have been calculated in our previous paper for n = 3 [

The numbers of stereoisomers of position A a and A c of C 3 H m 0 X m 1 Y m 2 Z m 3 having m 0 = 0 , m 1 ≠ 0 , m 2 ≠ 0 , m 3 ≠ 0 are equivalent to those of the system C n X m 1 Y m 2 Z m 3 given in our previous paper for n = 3 [

Using all these data, the inventory of stereoisomers of the heteropolyalkylated cyclopropane having two heteromorphous alkyl trees butyl ( i 4 = 1 ) and propyl ( i 3 = 2 ) is tabulated in

Representation of some graphs:

n = 3, m_{0} = 0, m_{1} = 4, m_{2} = 1, m_{3} = 1:

We have I R 3 = { A 3 , B 3 } , I R 4 = { A 4 , B 4 , C 4 , D 4 , D ′ 4 } , s 4 = 5 , p 4 = 3 , s 4 − p 4 = 2 , i 4 = 1 , s 3 = 2 , p 3 = 2 , s 3 − p 3 = 0 , i 3 = 2 then

m_{0} | m_{1} | m_{2} | m_{3} | A a | A c | A a a | A c a | A a c | A c c | A a a + c | A c a + c |
---|---|---|---|---|---|---|---|---|---|---|---|

1 | 1 | 1 | 3 | 0 | 10 | 0 | 30 | 0 | 0 | 0 | 20 |

1 | 1 | 2 | 2 | 2 | 14 | 6 | 42 | 0 | 0 | 4 | 28 |

0 | 1 | 1 | 4 | 1 | 2 | 3 | 6 | 0 | 0 | 2 | 4 |

0 | 1 | 2 | 3 | 2 | 4 | 6 | 12 | 0 | 0 | 4 | 8 |

0 | 2 | 2 | 2 | 4 | 7 | 12 | 21 | 0 | 0 | 8 | 14 |

N 3 , 4 = ( 2 2 ) ⋅ ( 5 1 ) = 5 which corresponds to groups of substituents A_{3}B_{3}A_{4}, A_{3}B_{3}B_{4}, A_{3}B_{3}C_{4}, A_{3}B_{3}D_{4}, A 3 B 3 D ′ 4 ; N 3 , 4 c = 0 , N 3 , 4 a = ( 2 2 ) ⋅ ( 3 1 ) = 3 which corresponds to the groups of substituents A_{3}B_{3}A_{4}, A_{3}B_{3}B_{4}, A_{3}B_{3}C_{4}; N 3 , 4 a + c = 5 − 3 = 2 which corresponds to groups of substituents A_{3}B_{3}D_{4}, A 3 B 3 D ′ 4 .

All those groups of substituents generate heteropolyalkylations of type C 4 H m 0 X m 1 Y m 2 Z m 3 such as m 0 + m 1 + m 2 + m 3 = 8 ; with the group de substituents A_{3}B_{3}C_{4} for example, we can make the assignment X = A 3 , Y = B 3 , Z = C 4 ; X = A 3 , Y = C 4 , Z = B 3 ; X = B 3 , Y = A 3 , Z = C 4 ; Z = B 3 , Y = C 4 , Z = A 3 ; X = C 4 , Y = A 3 , Z = B 3 ; X = C 4 , Y = B 3 , Z = A 3 .

The numbers of stereoisomers A a a , A c a , A a c , A c c , A a a + c and A c a + c are respectively obtained from the following formulas:

A a a = N 3 , 4 a × A a , A c a = N 3 , 4 a × A c , A a c = N 3 , 4 c × A a , A c c = N 3 , 4 c × A c , A a a + c = N 3 , 4 a + c × A a and A c a + c = N 3 , 4 a + c × A c where N 3 , 4 a = 3 , N 3 , 4 c = 0 and N 3 , 4 a + c = 2 .

The numbers of stereoisomers corresponding to placements or positions A a and A c of C 4 H m 0 X m 1 Y m 2 Z m 3 having m 0 ≠ 0 , m 1 ≠ 0 , m 2 ≠ 0 , m 3 ≠ 0 are equivalent to those of the system C n X m 1 Y m 2 Z m 3 U m 4 which have been calculated in our previous paper for n = 4 [

The numbers of stereoisomers of position A a and A c of C 4 H m 0 X m 1 Y m 2 Z m 3 having m 0 = 0 , m 1 ≠ 0 , m 2 ≠ 0 , m 3 ≠ 0 are equivalent to those of the system C n X m 1 Y m 2 Z m 3 calculated in our previous paper for n = 4 [

Using all these data, the inventory of stereoisomers of the heteropolyalkylated cyclobutane having heteromorphous radicals propyl (i_{3} = 2) and butyl (i_{4} = 1) is summarized in

We have I R 4 = { A 4 , B 4 , C 4 , D 4 , D ′ 4 } , I R 5 = { A 5 , B 5 , C 5 , D 5 , E 5 , E ′ 5 , F , F ′ 5 , G , G ′ 5 } , s 4 = 5 , p 4 = 3 , s 4 − p 4 = 2 , i 4 = 2 , s 5 = 11 , p 5 = 5 , s 5 − p 5 = 6 , i 5 = 2 ;

m_{0} | m_{1} | m_{2} | m_{4} | A a | A c | A a a | A c a | A a c | A c c | A a a + c | A c a + c |
---|---|---|---|---|---|---|---|---|---|---|---|

1 | 1 | 1 | 5 | 6 | 18 | 18 | 54 | 0 | 0 | 12 | 36 |

1 | 1 | 2 | 4 | 9 | 48 | 27 | 144 | 0 | 0 | 18 | 56 |

1 | 1 | 3 | 3 | 12 | 64 | 36 | 192 | 0 | 0 | 24 | 128 |

1 | 2 | 2 | 3 | 14 | 98 | 42 | 294 | 0 | 0 | 28 | 196 |

2 | 2 | 2 | 2 | 30 | 150 | 90 | 450 | 0 | 0 | 60 | 300 |

0 | 6 | 1 | 1 | 3 | 2 | 9 | 6 | 0 | 0 | 6 | 4 |

0 | 5 | 1 | 2 | 5 | 8 | 15 | 24 | 0 | 0 | 10 | 16 |

0 | 4 | 2 | 2 | 14 | 23 | 42 | 69 | 0 | 0 | 28 | 46 |

0 | 4 | 3 | 1 | 7 | 14 | 21 | 42 | 0 | 0 | 14 | 28 |

0 | 3 | 3 | 2 | 10 | 30 | 30 | 90 | 0 | 0 | 20 | 60 |

N 4 , 5 = ( 5 2 ) ⋅ ( 11 2 ) = 550 ; N 4 , 5 c = ( 2 2 ) ⋅ ( 6 2 ) = 15 which corresponds to groups of substituents D 4 D ′ 4 F 5 F ′ 5 , D 4 D ′ 4 F 5 G 5 , D 4 D ′ 4 F 5 G ′ 5 , D 4 D ′ 4 F 5 H 5 , D 4 D ′ 4 F 5 H ′ 5 , D 4 D ′ 4 F ′ 5 G 5 , D 4 D ′ 4 F ′ 5 G ′ 5 , D 4 D ′ 4 F ′ 5 H ′ 5 , D 4 D ′ 4 F ′ 5 H ′ 5 , D 4 D ′ 4 G 5 G ′ 5 , D 4 D ′ 4 G 5 H 5 , D 4 D ′ 4 G 5 H ′ 5 , D 4 D ′ 4 G ′ 5 H 5 , D 4 D ′ 4 G ′ 5 H ′ 5 , D 4 D ′ 4 G 5 H ′ 5 ; N 4 , 5 a = ( 3 2 ) ⋅ ( 5 2 ) = 30 ; N 4 , 5 a + c = 550 − 30 − 15 = 505 .

All the groups of substituents generate heteropolyalkylations of type C 3 H m 0 X m 1 Y m 2 Z m 3 U m 4 such as m 0 + m 1 + m 2 + m 3 + m 4 = 6 ; with the group de substituents A_{4}B_{4}C_{5}D_{5} for example, we can make the assignment X = A 4 , Y = B 4 , Z = C 5 , U = D 5 ; X = A 4 , Y = C 5 , Z = D 5 , U = B 4 ; X = B 4 , Y = A 4 , Z = D 5 , U = C 5 and so on. The numbers of stereoisomers A a a , A c a , A a c , A c c , A a a + c and A c a + c are respectively obtained from the following formulas:

A a a = N 4 , 5 a × A a , A c a = N 4 , 5 a × A c , A a c = N 4 , 5 c × A a , A c c = N 4 , 5 c × A c , A a a + c = N 4 , 5 a + c × A a and A c a + c = N 4 , 5 a + c × A c , with N 4 , 5 a = 30 , N 4 , 5 c = 15 , N 4 , 5 a + c = 505 .

The numbers of stereoisomers corresponding to placements or positions A a and A c of C 3 H m 0 X m 1 Y m 2 Z m 3 U m 4 having m 0 ≠ 0 , m 1 ≠ 0 , m 2 ≠ 0 , m 3 ≠ 0 ; m 4 ≠ 0 are equivalent to those of the system C n X m 1 Y m 2 Z m 3 U m 4 V m 5 determined in our previous paper for n = 3 [

The numbers of stereoisomers of position A a and A c of C 3 H m 0 X m 1 Y m 2 Z m 3 U m 4 having m 0 = 0 , m 1 ≠ 0 , m 2 ≠ 0 , m 3 ≠ 0 , m 4 ≠ 0 are equivalent to those of the system C n X m 1 Y m 2 Z m 3 U m 4 also derived in our previous paper for n = 3 [

Using all these data, the inventory of stereoisomers of the heteropolyalkylated cyclopropane having heteromorphous alkyl trees butyl ( i 4 = 2 ) and pentyl ( i 5 = 2 ) is summarized in

m_{0} | m_{1} | m_{2} | m_{3} | m_{4} | A a | A c | A a a | A c a | A a c | A c c | A a a + c | A c a + c |
---|---|---|---|---|---|---|---|---|---|---|---|---|

1 | 1 | 1 | 1 | 2 | 0 | 30 | 0 | 900 | 0 | 450 | 0 | 15,150 |

0 | 1 | 1 | 1 | 3 | 0 | 10 | 0 | 300 | 0 | 150 | 0 | 5050 |

0 | 1 | 1 | 2 | 2 | 2 | 14 | 60 | 420 | 30 | 210 | 1010 | 7070 |

We have I R 4 = { A 4 , B 4 , C 4 , D 4 , D ′ 4 } , I R 5 = { A 5 , B 5 , C 5 , D 5 , E 5 , E ′ 5 , F , F ′ 5 , G , G ′ 5 } , s 4 = 5 , p 4 = 3 , s 4 − p 4 = 2 , i 4 = 2 , s 5 = 11 , p 5 = 5 , s 5 − p 5 = 6 , i 5 = 2 ;

N 4 , 5 = ( 5 2 ) ⋅ ( 11 2 ) = 550 ; N 4 , 5 c = ( 2 2 ) ⋅ ( 6 2 ) = 15 which corresponds to groups of substituents D 4 D ′ 4 F 5 F ′ 5 , D 4 D ′ 4 F 5 G 5 , D 4 D ′ 4 F 5 G ′ 5 , D 4 D ′ 4 F 5 H 5 , D 4 D ′ 4 F 5 H ′ 5 , D 4 D ′ 4 F ′ 5 G 5 , D 4 D ′ 4 F ′ 5 G ′ 5 , D 4 D ′ 4 F ′ 5 H 5 , D 4 D ′ 4 F ′ 5 H ′ 5 , D 4 D ′ 4 G 5 G ′ 5 , D 4 D ′ 4 G 5 H 5 , D 4 D ′ 4 G 5 H ′ 5 , D 4 D ′ 4 G ′ 5 H 5 , D 4 D ′ 4 G ′ 5 H ′ 5 , D 4 D ′ 4 H 5 H ′ 5 ; N 4 , 5 a = ( 3 2 ) ⋅ ( 5 2 ) = 30 ; N 4 , 5 a + c = 550 − 30 − 15 = 505 .

All the groups of substituents generate heteropolyalkylations of type C 4 H m 0 X m 1 Y m 2 Z m 3 U m 4 such as m 0 + m 1 + m 2 + m 3 + m 4 = 8 ; with the group de substituents A_{4}B_{4}C_{5}D_{5} for example, we can make the assignment X = A 4 , Y = B 4 , Z = C 5 , U = D 5 ; X = A 4 , Y = C 5 , Z = D 5 , U = B 4 ; X = B 4 , Y = A 4 , Z = D 5 , U = C 5 and so on. The numbers of stereoisomers A a a , A c a , A a c , A c c , A a a + c and A c a + c are respectively obtained from the following formulas:

A a a = N 4 , 5 a × A a , A c a = N 4 , 5 a × A c , A a c = N 4 , 5 c × A a , A c c = N 4 , 5 c × A c , A a a + c = N 4 , 5 a + c × A a and A c a + c = N 4 , 5 a + c × A c , with N 4 , 5 a = 30 , N 4 , 5 c = 15 , N 4 , 5 a + c = 505 .

The numbers of stereoisomers corresponding to placements or positions A a and A c of C 4 H m 0 X m 1 Y m 2 Z m 3 U m 4 having m 0 ≠ 0 , m 1 ≠ 0 , m 2 ≠ 0 , m 3 ≠ 0 are equivalent to those of the system C n X m 1 Y m 2 Z m 3 U m 4 V m 5 which have been calculated in our previous paper for n = 4 [

The numbers of stereoisomers of position A a and A c of C 4 H m 0 X m 1 Y m 2 Z m 3 U m 4 having m 0 = 0 , m 1 ≠ 0 , m 2 ≠ 0 , m 3 ≠ 0 are equivalent to those of the system C n X m 1 Y m 2 Z m 3 U m 4 calculated in our previous paper for n = 4 [

Using all these data, the inventory of stereoisomers of the heteropolyalkylated cyclobutane having heteromorphous radicals butyl ( i 4 = 2 ) and pentyl ( i 5 = 2 ) is summarized in

The combinatorial method developed in the present paper makes it possible to

m_{0} | m_{1} | m_{2} | m_{3} | m_{4} | A a | A c | A a a | A c a | A a c | A c c | A a a + c | A c a + c |
---|---|---|---|---|---|---|---|---|---|---|---|---|

1 | 1 | 1 | 1 | 4 | 6 | 102 | 180 | 3060 | 90 | 1530 | 3030 | 51,510 |

1 | 1 | 1 | 2 | 3 | 12 | 204 | 360 | 6120 | 180 | 3060 | 6060 | 103,020 |

1 | 1 | 2 | 2 | 2 | 18 | 306 | 540 | 9180 | 270 | 4590 | 9090 | 154,530 |

0 | 1 | 1 | 1 | 5 | 6 | 18 | 180 | 540 | 90 | 270 | 3030 | 9090 |

0 | 1 | 1 | 2 | 4 | 9 | 48 | 270 | 1440 | 135 | 720 | 4545 | 24,240 |

0 | 1 | 1 | 3 | 3 | 12 | 64 | 360 | 1920 | 180 | 960 | 6060 | 32,320 |

0 | 1 | 2 | 2 | 3 | 14 | 98 | 420 | 2940 | 210 | 1470 | 7070 | 49,490 |

0 | 2 | 2 | 2 | 2 | 30 | 150 | 900 | 4500 | 450 | 2250 | 15,150 | 75,750 |

directly enumerate enantiomeric pairs and achiral skeletons of the heteropolyalkylated monocyclic cycloalkane R k α = C k α H 2 k α + 1 of which at least two noted alkyl groups each has a distinct order k α ( 1 ≤ α ≤ ζ ) . m α is the number of alkyl

radicals R k α in the system C n H m 0 ( R k 1 ) m 1 ⋯ ( R k α ) m α ⋯ ( R k ζ ) m ζ satisfying the relationship ∑ α = 1 ζ m α + m 0 = 2 n . This procedure has already been successfully applied

by Nemba and Balaban for the case of homomorphic heteropolyalkylation [

results of the system C n H m 0 ( R k 1 ) m 1 ⋯ ( R k α ) m α ⋯ ( R k ζ ) m ζ . In this work, we have

used the basic concepts of permutation group theory and algebraic combinatorics as tools to highlight the chirality and adequacy of achirality induced by composition of molecular systems through heteromorphic polyalkylation. The number of stereoisomers of this family of compounds evolves exponentially as a function of the number of asymmetric carbons of the molecular system carried not only by the radicals but also by the monocyclic cycloalkane. It is worth remembering that the compounds of this family of hydrocarbons serve as starting materials for extensive kinetic and mechanistic studies, while others are used successfully for important applications such as the manufacture of hydrocarbon resins and other chemicals. Hence the interest of the present scientific contribution.

This research was supported by the Ministry of Higher Education of the Republic of Cameroon through the modernization research allowances. Authors also thank the University of Yaounde’ I and High Teacher Training College (Cameroon) for the use of their infrastructural facilities.

The authors declare no conflicts of interest regarding the publication of this paper.

Emadak, A., Ndassa, I.M., Makon, B.T., Patouossa, I. and Nemba, R.M. (2019) Enumeration of Stereoisomers of Chiral and Achiral Derivatives of Monocyclic Cycloalkanes Having Heteromorphous Alkyl Substituents with Distinct Length k. Computational Chemistry, 7, 72-93. https://doi.org/10.4236/cc.2019.73006