Synthesis of 2‘,3‘-Didehydro-2‘,3‘-dideoxynucleosides by Reaction of 5‘-O-Protected Nucleoside 2‘,3‘-Dimesylates with Lithium Areneselenolates
Author:
Affiliation:
1. Chemistry Department, University of Alberta, Edmonton, Alberta, Canada T6G 2G2
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo962079p
Reference22 articles.
1. AIDS-driven nucleoside chemistry.
2. Synthesis of 2‘,3‘-Didehydro-2‘,3‘-dideoxynucleosides by Reaction of 5‘-Protected Nucleoside 2‘,3‘-Dimesylates with Telluride Dianion: A General Route from Cis Vicinal Diols to Olefins
3. Selenium stabilized carbanions. Preparation of .alpha.-lithio selenides and applications to the synthesis of olefins by reductive elimination of .beta.-hydroxy selenides and selenoxide syn elimination
4. .alpha. Vinylation of ketones. A general method using (phenylseleno)acetaldehyde
5. New regiospecific routes to olefins from β-hydroxy selenides
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