Michael Additions to (R)-1-Acetyl-5-isopropoxy-3-pyrrolin-2-one and Subsequent N-Acyliminium Ion Generation: Synthesis of Enantiopure 1-Azabicycles and Preparation of an Intermediate for a Projected Synthesis of Roseophilin-Reference-Cited by-同舟云学术

Michael Additions to (R)-1-Acetyl-5-isopropoxy-3-pyrrolin-2-one and Subsequent N-Acyliminium Ion Generation: Synthesis of Enantiopure 1-Azabicycles and Preparation of an Intermediate for a Projected Synthesis of Roseophilin

Published:1998-01-01 Issue:2 Volume:63 Page:220-221
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Luker Tim¹,Koot Wim-Jan¹,Hiemstra Henk¹,Speckamp W. Nico¹

Affiliation:

1. Laboratory of Organic Chemistry, Amsterdam Institute of Molecular Studies, University of Amsterdam, Nieuwe Achtergracht 129, 1018 WS Amsterdam, The Netherlands

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo971854d

Reference20 articles.

1. (R)-1-Acetyl-5-isopropoxy-3-pyrrolin-2-one: a versatile chiral dienophile from (S)-malic acid

2. Lipase-Catalyzed Second-Order Asymmetric Transformations as Resolution and Synthesis Strategies for Chiral 5-(Acyloxy)-2(5H)-furanone and Pyrrolinone Synthons

3. (a) Koot, W.J.; Hiemstra, H.; Speckamp, W. N.Tetrahedron: Asymmetry1993,4, 1941.

4. Stereoselective synthesis of enantiopure 4,5-disubstituted pyrrolidin-2-ones by consecutive cuprate addition and N-acyliminium coupling

5. Stereochemistry of allylic alkylation of the tetracarbonyliron complexes of (R)-1-acetyl-5-isopropoxy-3-pyrrolin-2-one

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