Stereoselective Synthesis of Densely Functionalized Pyrrolidin-2-ones by a Conjugate Addition/Nitro-Mannich/Lactamization Reaction-Reference-Cited by-同舟云学术

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Stereoselective Synthesis of Densely Functionalized Pyrrolidin-2-ones by a Conjugate Addition/Nitro-Mannich/Lactamization Reaction

Published:2012-06-28 Issue:14 Volume:77 Page:6186-6198
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Anderson James C.¹,Horsfall Lisa R.¹,Kalogirou Andreas S.¹,Mills Matthew R.¹,Stepney Gregory J.²,Tizzard Graham J.³

Affiliation:

1. Department of Chemistry, University College London, 20 Gordon Street, London WC1H 0AJ, U.K.

2. School of Chemistry, University of Nottingham, Nottingham NG7 2RD, U.K

3. National Crystallography Service, School of Chemistry, University of Southampton, Southampton SO17 1BJ, U.K.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo301000r

Reference58 articles.

1. The Nitro-Mannich Reaction and Its Application to the Stereoselective Synthesis of 1,2-Diamines

2. The First Catalytic Asymmetric Nitro-Mannich-Type Reaction Promoted by a New Heterobimetallic Complex

3. The First Catalytic Asymmetric Aza-Henry Reaction of Nitronates with Imines: A Novel Approach to Optically Active β-Nitro-α-Amino Acid- and α,β-Diamino Acid Derivatives

4. Enantioselective Aza-Henry Reaction Catalyzed by a Bifunctional Organocatalyst

5. An Asymmetric Nitro-Mannich Reaction Applicable to Alkyl, Aryl, and Heterocyclic Imines

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