Trifluoromethanesulfonic Acid, an Unusually Powerful Catalyst for the Michael Addition Reaction of β-Ketoesters under Solvent-Free Conditions-Reference-Cited by-同舟云学术

Trifluoromethanesulfonic Acid, an Unusually Powerful Catalyst for the Michael Addition Reaction of β-Ketoesters under Solvent-Free Conditions

Published:1999-04-16 Issue:10 Volume:64 Page:3770-3773
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Kotsuki Hiyoshizo¹,Arimura Koji¹,Ohishi Takeshi¹,Maruzasa Ryosuke¹

Affiliation:

1. Department of Chemistry, Faculty of Science, Kochi University, Akebono-cho, Kochi 780-8520, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo982521z

Reference25 articles.

1. Bergman, E. D.; Ginsburg, D.; Pappo, R.Org. React.1959,10, 595. House, H. O.Modern Synthetic Reactions, 2nd ed.; W. A. Benjamin, Inc. Menlo Park, 1972; pp 595−623. Jung, M. E. InComprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon: Oxford, 1991; Vol. 4, pp 1−67. Perlmutter, P.Conjugate Addition Reactions in Organic Synthesis; Pergamon Press: Oxford, 1992.

2. Yb(OTf)3-CATALYZED MICHAEL ADDITION REACTIONS OF β-KETOESTERS ON SILICA GEL SUPPORTS AND AT HIGH PRESSURE

3. Trifluoromethanesulfonic acid and derivatives

4. Catalytic C-amidoalkylations: synthesis of β-amido aldehydes by three-component condensations

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