Rapid Improvement of a Reductive Sulfonylation Using Design of Experiment Methods
Author:
Affiliation:
1. Early Process Research and Development, Pharmacia, Kalamazoo, Michigan 49001, U.S.A., and Chemical Development, SUGEN, Inc., South San Francisco, California 94080, U.S.A.
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/op034018g
Reference9 articles.
1. Drabowicz, J.; Kielbasinski, P.; Mikolajczyk, M. InThe Chemistry ofSulphinic Acids, Esters and Their Derivatives; Patai, S., Ed.; John Wiley & Sons: New York, 1990; p 351−430.
2. A convenient method for the synthesis of β, γ-unsaturated sulfones through zinc-mediated CS coupling reaction
3. A Convenient Synthesis of Sulfones Using Zinc Mediated Coupling Reaction of Sulfonyl Chlorides with Alkyl Halides in Aqueous Media
4. Aluminum Chloride–Iron Promoted Coupling of Sulfonyl Chlorides with Alkyl Halides in Aqueous Media
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