Enantioselective Multicomponent Reaction for Rapid Construction of 1,2,5-Triol Derivatives with Vicinal Chiral Centers-Reference-Cited by-同舟云学术

Enantioselective Multicomponent Reaction for Rapid Construction of 1,2,5-Triol Derivatives with Vicinal Chiral Centers

Published:2017-05-01 Issue:10 Volume:82 Page:5212-5221
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Li Mingfeng¹,Guo Xin¹,Zheng Qing¹,Hu Wenhao¹^ORCID,Liu Shunying¹^ORCID

Affiliation:

1. Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai 200062, China

Funder

Science and Technology Commission of Shanghai Municipality

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.7b00473

Reference34 articles.

1. Stereoselective construction of skipped polyol enabled by oxonia-Cope rearrangement and iodolactonization: enantioselective synthesis of (+)-yashabushitriol

2. Stereoselective synthesis of carbocyclic analogues of the nucleoside Q precursor (PreQ0)

3. A General Strategy for the Synthesis of Cladiellin Diterpenes: Enantioselective Total Syntheses of 6-Acetoxycladiell-7(16),11-dien-3-ol (Deacetoxyalcyonin Acetate), Cladiell-11-ene-3,6,7-triol, Sclerophytin A, and the Initially Purported Structure of Sclerophytin A

4. An Alkyne Strategy for the Asymmetric Synthesis of Natural Products: Application to (+)-Spirolaxine Methyl Ether

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