Tandem Nitroaldol−Dehydration Reactions Employing the Dianion of Phenylsulfonylnitromethane1
Author:
Affiliation:
1. Department of Chemistry, Drexel University, Philadelphia, Pennsylvania 19104, and Department of Chemistry, University of Pennsylvania, Philadelphia, Pennsylvania 19104
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo0000170
Reference17 articles.
1. .alpha.-Nitro sulfones. 2. Convenient new synthesis and selected functional group transformations
2. The Taft equation as applied to equilibrium acidities of nitroalkanes, G(CH2)nNO2
3. Chemistry of .alpha.-nitro sulfones. IV. Functionalization at the activated carbon
4. Preparation of .alpha.-substituted S-phenyl thio esters from aldehydes and (phenylthio)nitromethane
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