Asymmetric Synthesis of Neolignans (−)-epi-Conocarpan and (+)-Conocarpan via Rh(II)-Catalyzed C−H Insertion Process and Revision of the Absolute Configuration of (−)-epi-Conocarpan-Reference-Cited by-同舟云学术

Asymmetric Synthesis of Neolignans (−)-epi-Conocarpan and (+)-Conocarpan via Rh(II)-Catalyzed C−H Insertion Process and Revision of the Absolute Configuration of (−)-epi-Conocarpan

Published:2009-05-01 Issue:11 Volume:74 Page:4418-4421
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Natori Yoshihiro¹,Tsutsui Hideyuki¹,Sato Naoki¹,Nakamura Seiichi¹,Nambu Hisanori¹,Shiro Motoo¹,Hashimoto Shunichi¹

Affiliation:

1. Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812, Japan, and Rigaku Corporation, Akishima, Tokyo 196-8666, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo900502d

Reference54 articles.

1. New lignans in Conocarpus erectus

2. Phenylpropanoids and neolignans from Piper regnellii

3. Isolation of a Dihydrobenzofuran Lignan from South American Dragon's Blood (Croton spp.) as an Inhibitor of Cell Proliferation

4. Brugnanin, a new syn-2,3-dihydrobenzofuran neolignan dioate from the mangrove Bruguiera gymnorrhiza

5. Lignans and neolignans as lead compounds

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