Asymmetric Methoxyselenenylation of Alkenes with Chiral Ferrocenylselenium Reagents
Author:
Affiliation:
1. Department of Applied Chemistry, Chuo University, Kasuga, Bunkyo-ku, Tokyo 112, Japan
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo970982z
Reference23 articles.
1. Asymmetric oxidation of simple selenides to selenoxides in high enantiopurity. Stereochemical aspects of the allyl selenoxide/allyl selenenate rearrangement
2. A highly selective asymmetric methoxyselenylation of alkenes with a chiral ferrocenylselenium reagent
3. Rhodium(I)-catalysed asymmetric hydrosilylation of ketones using new diferrocenyl dichalcogenides (R,S)-{[EC5H3CHMe(NMe2)]Fe(C5H5)}2(E = S, Se, Te), as chiral ligands
4. Asymmetric selenomethoxylation of olefins involving a chiral C2 symmetrical electrophilic organoselenium reagent
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