Total Synthesis of Aculeatins A and B, and Formal Synthesis of Aculeatin D and 6-epi-Aculeatin D through an Asymmetric Aldol Reaction-Reference-Cited by-同舟云学术

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Total Synthesis of Aculeatins A and B, and Formal Synthesis of Aculeatin D and 6-epi-Aculeatin D through an Asymmetric Aldol Reaction

Published:2015-02-26 Issue:09 Volume:47 Page:1303-1308
ISSN:0039-7881
Container-title:Synthesis
language:en
Short-container-title:Synthesis

Author:

Wang Xiaoji¹,Huang Shuangping¹,Chen Shipeng¹,Wang Gaopeng¹,Zhang Jianting¹,Tang Linjun²,Du Guangyan³

Affiliation:

1. School of Pharmacy, Jiangxi Science and Technology Normal University

2. School of Life Science, Jiangxi Science and Technology Normal University

3. Laboratory of Chemical Genomics, School of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate School

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry,Catalysis

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0034-1380228.pdf

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. PIDA-Promoted/HFIP-Controlled Dearomative Spirocyclization of Phenolic Ketones via a Spirocyclohexadienone-Oxocarbenium Cation Species;The Journal of Organic Chemistry;2022-04-23

2. A novel total synthesis of aculeatin A via a stepwise approach;RSC Advances;2017

3. Recent developments in total syntheses of aculeatins;Tetrahedron Letters;2016-09

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