The applications of catalytic asymmetric halocyclization in natural product synthesis

Author:

Yan Jiahang1,Zhou Zhiqiang1,He Qiaoqiao1,Chen Guzhou1,Wei Hongbo1ORCID,Xie Weiqing12ORCID

Affiliation:

1. Shaanxi Key Laboratory of Natural Products & Chemical Biology, College of Chemistry & Pharmacy, Northwest A&F University, 22 Xinong Road, Yangling 712100, Shaanxi, China

2. Key Laboratory of Botanical Pesticide R&D in Shaanxi Province, Yangling, Shaanxi 712100, China

Abstract

Catalytic asymmetric halocyclization of olefinic substrate has evolved rapidly and been well utilized as a practical strategy for constructing enantioenriched cyclic skeletons in natural product synthesis.

Funder

Northwest A and F University

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Reference230 articles.

1. K. E.Harding and T. H.Tiner , in Comprehensive Organic Synthesis , ed. B. M. Trost and I. Fleming , Pergamon Press , Oxford , 1991 , vol. 4 , p. 363

2. J.Mulzer , in Organic Synthesis Highlights , ed. J. Mulzer , H. J. Altenbach , M. Braun , K. Krohn and H. U. Reissig , VCH , Weinheim , 1991 , p. 157

3. F.Rodríguez and F. J.Fañanás , in Handbook of Cyclization Reactions , ed. S. Ma , Wiley-VCH , New York , 2010 , vol. 4 , pp. 951–990

4. Synthesis and synthetic utility of halolactones

5. Stereocontrolled cyclofunctionalizations of double bonds through heterocyclic intermediates

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