Synthesis of (+)-Febrifugine and a Formal Synthesis of (+)-Halofuginone Employing an Organocatalytic Direct Vinylogous Aldol Reaction-Reference-Cited by-同舟云学术

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Synthesis of (+)-Febrifugine and a Formal Synthesis of (+)-Halofuginone Employing an Organocatalytic Direct Vinylogous Aldol Reaction

Published:2013-05-08 Issue:13 Volume:45 Page:1863-1869
ISSN:0039-7881
Container-title:Synthesis
language:en
Short-container-title:Synthesis

Author:

Pansare Sunil,Paul Eldho

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry,Catalysis

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0033-1338706.pdf

Cited by 18 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. Synthesis and Evaluation of N-Diaminophosphoryl Aminothioureas as Bifunctional Catalysts for Vinylogous Aldol Reactions of Isatins and 2(3H)-Furanones;ACS Omega;2023-01-09

2. Stereoselective synthesis of analogues of deoxyfebrifugine;Journal of Chemical Research;2022-01

3. Enantiodivergent Synthesis of Halofuginone by Candida antarctica Lipase B (CAL-B)-Catalyzed Kinetic Resolution in Cyclopentyl Methyl Ether (CPME);SynOpen;2021-06

4. Stereoselective total synthesis of all the stereoisomers of (+)- and (−)-febrifugine and halofuginone;Tetrahedron Letters;2020-07

5. TiCl 4 ‐Et 3 N‐mediated one‐step synthesis of γ‐alkylidenebutenolides from ketones: Application to natural product synthesis;Journal of Heterocyclic Chemistry;2020-04

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