Highly Stereoselective Direct Construction of Diaryl‐Substituted Cyclobutanes †-Reference-Cited by-同舟云学术

Highly Stereoselective Direct Construction of Diaryl‐Substituted Cyclobutanes †

Published:2020-01-10 Issue:3 Volume:38 Page:259-262
ISSN:1001-604X
Container-title:Chinese Journal of Chemistry
language:en
Short-container-title:Chin. J. Chem.

Author:

Song Xiang‐Yang¹,Zhao Liu‐Peng¹,Wang Lijia¹²,Tang Yong¹

Affiliation:

1. State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, University of Chinese Academy of Sciences 345 Lingling Lu Shanghai 200032 China

2. Shanghai Key Laboratory of Green Chemistry and Chemical Processes, Department of Chemistry, East China Normal University 3663 North Zhongshan Road Shanghai 200062 China

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cjoc.201900456

Reference42 articles.

1. For selected examples see: (a)Nakamura M.;Chi Y. M.;Yan W.‐M.;Yonezawa A.;Nakasugi Y.;Yoshizawa T.;Hashimoto F.;Kinjo J.;Nohara T.;Sakurada S.Structure‐antinociceptive activity studies of incarvillateine a monoterpene alkaloid from incarvillea sinensis.Planta Med.2001 67 114–117;

2. Two new alkaloids, pipercyclobutanamides A and B, from Piper nigrum

3. Cyclobutanoid Amides fromPiper arborescens

4. Nigramides A−S, Dimeric Amide Alkaloids from the Roots of Piper nigrum

5. New Cytotoxic Cyclobutanoid Amides, a New Furanoid Lignan and Anti-Platelet Aggregation Constituents fromPiper arborescens

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