C–H functionalization of cyclic amines: redox-annulations with α,β-unsaturated carbonyl compounds-Reference-Cited by-同舟云学术

C–H functionalization of cyclic amines: redox-annulations with α,β-unsaturated carbonyl compounds

Published:2015 Issue:53 Volume:51 Page:10648-10651
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Kang YoungKu¹²³⁴⁵,Richers Matthew T.¹²³⁴⁵,Sawicki Conrad H.¹²³⁴⁵,Seidel Daniel¹²³⁴⁵

Affiliation:

1. Department of Chemistry and Chemical Biology

2. Rutgers

3. The State University of New Jersey

4. Piscataway

5. USA

Abstract

Pyrrolidine and related amines undergo carboxylic acid promoted redox-annulations with α,β-unsaturated ketonesviathe intermediacy of conjugated azomethine ylides.

Funder

National Institutes of Health

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2015/CC/C5CC03390J

Reference105 articles.

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4. A. Padwa , 1,3-Dipolar Cycloaddition Chemistry, Wiley, New York, N.Y., 1984, vol. 1

5. 1,3-Dipolar Cycloaddition Chemistry, ed. A. Padwa, Wiley, New York, N.Y., 1984, vol. 2

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