Catalytic Asymmetric Synthesis of the endo-6-Aryl-8-oxabicyclo[3.2.1]oct-3-en-2-one Natural Product from Ligusticum chuanxing via 1,3-Dipolar Cycloaddition of a Formyl-Derived Carbonyl Ylide Using Rh2(S-TCPTTL)4-Reference-Cited by-同舟云学术

Catalytic Asymmetric Synthesis of the endo-6-Aryl-8-oxabicyclo[3.2.1]oct-3-en-2-one Natural Product from Ligusticum chuanxing via 1,3-Dipolar Cycloaddition of a Formyl-Derived Carbonyl Ylide Using Rh2(S-TCPTTL)4

Published:2010-08-11 Issue:17 Volume:75 Page:6039-6042
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Shimada Naoyuki¹,Hanari Taiki¹,Kurosaki Yasunobu¹,Takeda Koji¹,Anada Masahiro¹,Nambu Hisanori¹,Shiro Motoo²,Hashimoto Shunichi¹

Affiliation:

1. Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812, Japan

2. Rigaku Corporation, Akishima, Tokyo 196-8666, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo101175b

Reference74 articles.

1. Two New Lactones and One New Aryl-8-oxa-bicyclo[3,2,1]oct-3-en-2-one from Descurainia sophia

2. Cartorimine, a New Cycloheptenone Oxide Derivative from Carthamus tinctorius

3. Synthesis of (±)-cartorimine

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