International Journal of Organic Chemistry

Volume 2, Issue 4 (December 2012)

ISSN Print: 2161-4687   ISSN Online: 2161-4695

Google-based Impact Factor: 1.26  Citations  

An Efficient Reaction Process for the Synthesis of Oxazinanes, and Oxazolidines in the Presence of Air

HTML  XML Download Download as PDF (Size: 147KB)  PP. 362-365  
DOI: 10.4236/ijoc.2012.24049    5,635 Downloads   8,851 Views  Citations

ABSTRACT

After purging air through the mixture of aldehydes and amino alcohols and microwaved the reaction mixture at 50°C for minutes gave the corresponding oxazinanes, and oxazolidines in excellent yields.

Share and Cite:

Al-Masum, M. , Lott, B. and Ghazialsharif, N. (2012) An Efficient Reaction Process for the Synthesis of Oxazinanes, and Oxazolidines in the Presence of Air. International Journal of Organic Chemistry, 2, 362-365. doi: 10.4236/ijoc.2012.24049.

Cited by

[1] Identificación de los productos de reacción de monoetanolamina y formaldehido en un reactor semibatch a 20, 30 y 40° C
2019
[2] IDENTIFICACIÓN DE LOS PRODUCTOS DE REACCIÓN DE MONOETANOLAMINA Y FORMALDEHÍDO EN UN REACTOR SEMIBATCH A 20, 30 Y 40 C
2018
[3] Design and synthesis of novel thiourea metal complexes with controllable antibacterial properties
Applied Organometallic Chemistry, 2018
[4] Further study of oxazolidines derived from mefloquine and arenealdehydes: diastereoisomers and polymorphs
Zeitschrift für Kristallographie-Crystalline Materials, 2016
[5] One pot InCl 3-catalyzed synthesis of 1-glycosylmethyl-1H-imidazoles
Tetrahedron, 2016
[6] Fe-catalyzed synthesis of substituted N-aryl oxazolidines
Organic & Biomolecular Chemistry, 2016
[7] One pot InCl3-catalyzed synthesis of 1-glycosylmethyl-1H-imidazoles
Tetrahedron, 2016
[8] MICROWAVE ASSISTED SYNTHESIS OF 4-SUBSTITUTED POLYHYDROXLIDENE-2-PHENYL OXAZOLIDINE-5-ONES
2015

Copyright © 2024 by authors and Scientific Research Publishing Inc.

Creative Commons License

This work and the related PDF file are licensed under a Creative Commons Attribution 4.0 International License.