A General Strategy for the Diastereoselective Synthesis of 2,6-Diaryl-3,7-dioxabicyclo[3.3.0]octane Lignans-Reference-Cited by-同舟云学术

A General Strategy for the Diastereoselective Synthesis of 2,6-Diaryl-3,7-dioxabicyclo[3.3.0]octane Lignans

Published:2003-10-24 Issue:23 Volume:68 Page:9159-9161
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Aldous David J.¹,Dalençon Anne J.¹,Steel Patrick G.¹

Affiliation:

1. Department of Chemistry, University of Durham, South Road, Durham, DH1 3LE, UK, and Aventis Pharma, Inc., Route 202-206, P.O. Box 6800, Bridgewater, New Jersey 08807 p.g.steel@durham.ac.uk

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo035148q

Reference11 articles.

1. Asymmetric syntheses of lignans utilizing novel diastereoselective Michael addition of cyanohydrin: Syntheses of (+)-fargesin and (−)-picropodophyllone

2. First Stereocontrolled Syntheses of Unsymmetrically Substituted Bislactone Lignans: Stereocontrolled Syntheses of Four Possible Isomers of Methyl 4,8-Dioxoxanthoxylol

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