Regiospecific 6-Endo-Annulation of in Situ Generated 3,4-Dienamides/Acids: Synthesis of δ-Lactams and δ-Lactones-Reference-Cited by-同舟云学术

Regiospecific 6-Endo-Annulation of in Situ Generated 3,4-Dienamides/Acids: Synthesis of δ-Lactams and δ-Lactones

Published:2013-05-13 Issue:11 Volume:15 Page:2608-2611
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Liu Ying¹,Barry Badru-Deen¹,Yu Haifeng¹,Liu Jianquan¹,Liao Peiqiu¹,Bi Xihe¹

Affiliation:

1. Department of Chemistry, Northeast Normal University, Changchun 130024, P. R. of China, State Key Laboratory of Elemento-Organic Chemistry, Nankai University, Tianjin 300071, P. R. of China, and School of Chemistry and Life Science, Anshan Normal University, Anshan, Liaoning 114007, P. R. of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol4007772

Reference66 articles.

1. Synthesis of 2,6-Dideoxysugars via Ring-Closing Olefinic Metathesis

2. Rhodium(I)-Catalyzed Allenic Carbocyclization Reaction Affording δ- and ε-Lactams

3. Catalytic Asymmetric Access to α,β Unsaturated δ-Lactones through a Vinylogous Aldol Reaction: Application to the Total Synthesis of the Prelog-Djerassi Lactone

4. Participation of the β-hydroxyketone part for potent cytotoxicity of callystatin A, a spongean polyketide

5. Synthesis and evaluation of delta lactams as nonpeptide HIV-protease inhibitors

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