Stereochemistry of the Benzylidene γ-Butyrolactone Dictates the Reductive Heck Cyclization Mode in the Asymmetric Synthesis of Aryltetralin Lignans: A Detailed Experimental and Theoretical Study-Reference-Cited by-同舟云学术

Stereochemistry of the Benzylidene γ-Butyrolactone Dictates the Reductive Heck Cyclization Mode in the Asymmetric Synthesis of Aryltetralin Lignans: A Detailed Experimental and Theoretical Study

Published:2022-02-08 Issue:6 Volume:87 Page:3910-3921
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Sen Biswajit¹,Roy Saikat²,Garai Sujay¹²,Roy Sayan¹,Anoop Anakuthil²^ORCID,Hajra Saumen¹^ORCID

Affiliation:

1. Center of Biomedical Research, Sanjay Gandhi Post-Graduate Institute of Medical Sciences Campus, Raebareli Road, Lucknow 226014, India

2. Department of Chemistry, Indian Institute of Technology Kharagpur, Kharagpur 721302, India

Funder

Science and Engineering Research Board

Department of Science and Technology, Ministry of Science and Technology

Council for Scientific and Industrial Research

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.1c02174

Reference34 articles.

1. An update on bioactive plant lignans

2. Lignans and Human Health

3. Naturally occurring furofuran lignans: structural diversity and biological activities

4. The Clinical Pharmacology of Etoposide and Teniposide

5. Synthesis and Characterization of Podophyllotoxin Analogues

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