Highly Enantioselective Synthesis of Functionalized Glutarimide Using Oxidative N-Heterocyclic Carbene Catalysis: A Formal Synthesis of (−)-Paroxetine-Reference-Cited by-同舟云学术

Highly Enantioselective Synthesis of Functionalized Glutarimide Using Oxidative N-Heterocyclic Carbene Catalysis: A Formal Synthesis of (−)-Paroxetine

Published:2019-03-18 Issue:9 Volume:84 Page:5313-5327
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Porey Arka¹,Santra Surojit¹,Guin Joyram¹^ORCID

Affiliation:

1. School of Chemical Sciences, Indian Association for the Cultivation of Science, 2A & 2B Raja S. C. Mullick Road, Jadavpur, Kolkata 700032, India

Funder

Council of Scientific and Industrial Research

Science and Engineering Research Board

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.9b00320

Reference59 articles.

1. A concise formal total synthesis of lactimidomycin

2. A new glutarimide derivative from marine sponge-derived Streptomyces anulatus S71

3. Multifaceted Modes of Action for the Glutarimide-Containing Polyketides Revealed

4. Synthesis, structures and anti-HBV activities of derivatives of the glutarimide antibiotic cycloheximide

5. The evolution of thalidomide and its IMiD derivatives as anticancer agents

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