Controlling the Facial Selectivity of Asymmetric [4 + 2] Cyclo-additions: A Concise Synthesis of the cis-Decalin Core Structure of Superstolides A and B-Reference-Cited by-同舟云学术

Controlling the Facial Selectivity of Asymmetric [4 + 2] Cyclo-additions: A Concise Synthesis of the cis-Decalin Core Structure of Superstolides A and B

Published:2011-06-14 Issue:14 Volume:13 Page:3580-3583
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Chen Lei¹,Hua Zhengmao¹,Li Gangqin¹,Jin Zhendong¹

Affiliation:

1. Division of Medicinal and Natural Products Chemistry, Department of Pharmaceutical Sciences and Experimental Therapeutics, College of Pharmacy, The University of Iowa, Iowa City, Iowa 52242, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol201095b

Reference47 articles.

1. An Expedient Asymmetric Synthesis of Platencin

2. Biomimetic Total Synthesis of Bisorbicillinol, Bisorbibutenolide, Trichodimerol, and Designed Analogues of the Bisorbicillinoids

3. Lycopladine H, a novel alkaloid with fused-tetracyclic skeleton from Lycopodium complanatum

4. Structure and Neurotrophic Activity of seco-Prezizaane-Type Sesquiterpenes from Illicium merrillianum

5. An enantiospecific total synthesis of (−)-patchouli alcohol

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