Enantioselective Catalytic Desymmetrization of Maleimides by Temporary Removal of an Internal Mirror Plane and Stereoablative Over-reduction: Synthesis of (R)-Pyrrolam A-Reference-Cited by-同舟云学术

Enantioselective Catalytic Desymmetrization of Maleimides by Temporary Removal of an Internal Mirror Plane and Stereoablative Over-reduction: Synthesis of (R)-Pyrrolam A

Published:2014-06-27 Issue:14 Volume:16 Page:3780-3783
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Marsh Barrie J.¹,Adams Harry¹,Barker Mike D.²,Kutama Ibrahim U.¹,Jones Simon¹

Affiliation:

1. Department of Chemistry, University of Sheffield, Dainton Building, Brook Hill, Sheffield S3 7HF, United Kingdom

2. Medicines Research Centre, GlaxoSmithKline Research and Development Ltd., Gunnels Wood Road, Stevenage, Hertfordshire SG1 2NY, United Kingdom

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol5016702

Reference25 articles.

1. Enantioselective desymmetrisation

2. AN ASYMMETRIC SYNTHESIS OF BICYCLIC LACTONES AND ITS APPLICATION TO THE ASYMMETRIC SYNTHESIS OF (1R,3S)-CIS-CHRYSANTHEMIC ACID

3. Highly selective formation of cis-substituted hydroxylactams via auxiliary-controlled reduction of imides

4. Highly Enantioselective Reduction of meso-Cyclic-1,2-dicarboximides. Asymmetric Synthesis of Bicyclic 2-Pyrrolidinone and Its 5-Hydroxy Congener

5. Enantioselective Reduction of meso-Cyclic-1,2-dicarboxylic Anhydrides and 1,2-Dicarboximides: Asymmetric Synthesis of Bicyclic Lactones and Hydroxylactams.

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