Improved Conditions for Facile Overman Rearrangement1
Author:
Affiliation:
1. Laboratory of Organic Chemistry, School of Bioagricultural Sciences, Nagoya University, Chikusa, Nagoya 464-01, Japan
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo9713924
Reference26 articles.
1. This study was presented at the annual meeting of Japan Society for Bioscience, Biotechnology and Agrochemistry, Abstract. p 119, Tokyo, Japan, April, 1997.
2. Molecular orbital theory of the electronic structure of organic compounds. XX. Protonated cyclopropane cations with a polarized basis set
3. Chlorocyanation of barrelenes as a route to 1-cyanosemibullvalenes. Convenient introduction of an efficient .pi.-electron acceptor substituent and its influence on the Cope equilibrium
4. Allylic and propargylic imidic esters in organic synthesis
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