Literature DB >> 21879702

Concise asymmetric total synthesis of 9-epi-sessilifoliamide J.

Shi-Chuan Tuo1, Jian-Liang Ye, Ai-E Wang, Su-Yu Huang, Pei-Qiang Huang.   

Abstract

A 10-step asymmetric synthesis of 9-epi-sessilifoliamide J (20), together with sessilifoliamide J (6), has been accomplished from the key chiral building block 11 via a threo-selective vinylogous Mannich reaction and a Ley oxidation-SmI(2)-mediated coupling lactonization. The absolute configuration of the natural sessilifoliamide J was established.
© 2011 American Chemical Society

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Year:  2011        PMID: 21879702     DOI: 10.1021/ol202140y

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  1 in total

1.  Oxidations of pyrrolidines and piperidines to afford CH-functionalized isopropyl-1-carboxylate congeners.

Authors:  Steven Gunawan; Nathan Bedard; Christopher Foley; Christopher Hulme
Journal:  Tetrahedron Lett       Date:  2021-03-17       Impact factor: 2.415

  1 in total

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