Honda, K., Lopez, S.A., Houk, K.N. and Mikami, K. (2015) Mono-, Di-, and Trifluoromethyl Substituent Effects on the Torquoselectivities of Cyclobutene and Oxeteneelectrocyclic Ring Openings. J. Org. Chem., 80, 11768-11772. https://doi.org/10.1021/acs.joc.5b01361

has been cited by the following article:

• TITLE: Orbital Phase Theory and the Diastereoselectivity of Some Organic Reactions

  AUTHORS: Yuji Naruse

  KEYWORDS: Orbital Phase Theory, Diastereoselectivity, Orbital Phase Continuity, Bond Model Analysis

  JOURNAL NAME: Journal of Materials Science and Chemical Engineering, Vol.6 No.7, July 4, 2018

  ABSTRACT: The orbital phase refers to the relationship between orbitals that originates from their wave character. We show here that the orbital phase essentially determines the diastereoselectivity of the following three organic reactions. 1) Torquoselectivity of the electrocyclicring-opening reaction of 3-substituted cyclobutenes; 2) Contradictory torquoselectivity of the retro-Nazarov reaction; 3) Diastereoselectivity in electrophilic addition to substituted ethylenes.