N[1,3]-sigmatropic shift in the benzidine rearrangement: experimental and theoretical investigation-Reference-Cited by-同舟云学术

N[1,3]-sigmatropic shift in the benzidine rearrangement: experimental and theoretical investigation

Published:2014 Issue:27 Volume:12 Page:4952-4963
ISSN:1477-0520
Container-title:Org. Biomol. Chem.
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Hou Shili¹²³⁴⁵,Li Xinyao¹²³⁴⁵,Xu Jiaxi¹²³⁴⁵

Affiliation:

1. State Key Laboratory of Chemical Resource Engineering

2. Department of Organic Chemistry

3. Faculty of Science

4. Beijing University of Chemical Technology

5. Beijing 100029, People's Republic of China

Abstract

The N[1,3]-sigmatropic shift with an inversion of the configuration in the migrating nitrogen atom exists in the formation of semidines and diphenyline.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/OB/C4OB00080C

Reference88 articles.

1. The Hydroallylation of Olefins via Hydroboration of Propargyl Chloride

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4. Allylborane and its isomers. An ab initio study of the C3BH7 potential energy surface, the barrier to 1,3-shifts in allylboranes, and nonclassical boracyclobutane, cyclopropylborane, and vinylborane structures

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