Enantioselective Formal [4+1] Cycloaddition of Diazoarylacetates and the Danishefsky’s Diene: Stereoselective Synthesis of (−)-1,13-Herbertenediol-Reference-Cited by-同舟云学术

Enantioselective Formal [4+1] Cycloaddition of Diazoarylacetates and the Danishefsky’s Diene: Stereoselective Synthesis of (−)-1,13-Herbertenediol

Published:2018-09-14 Issue:20 Volume:83 Page:12806-12814
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Hu Fang¹,Zhou Qing¹,Cao Fei¹,Chu Wen-Dao¹^ORCID,He Long¹,Liu Quan-Zhong¹

Affiliation:

1. Chemical Synthesis and Pollution Control, Key Laboratory of Sichuan Province, College of Chemistry and Chemical Engineering, China West Normal University, No 1, Shida Road, Nanchong 637002, People’s Republic of China

Funder

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.8b01546

Reference41 articles.

1. The synthesis of compounds related to the indole–indoline core of the vinca alkaloids (+)-vinblastine and (+)-vincristine

2. Asymmetric synthesis of the core cyclopentane of viridenomycin

3. Stereoselective Synthesis of 4'-.ALPHA.-Alkylcarbovir Derivatives Based on an Asymmetric Synthesis or Chemoenzymatic Procedure.

4. A Formal Total Synthesis of (±)-1,13-Herbertenediol

5. Herbertane-type sesquiterpenoids from the liverwort Herbertus sakuraii

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