Literature DB >> 19320459

Formal syntheses of (+/-)-stemonamine and (+/-)-cephalotaxine.

Yu-Ming Zhao1, Peiming Gu, Hai-Jun Zhang, Qing-Wei Zhang, Chun-An Fan, Yong-Qiang Tu, Fu-Min Zhang.   

Abstract

A short and efficient approach to aza-quaternary pyrrolo[1,2-a]azepine 8 and aza-quaternary indolizine 23, as the crucial intermediates for syntheses of stemonamine (1a) and cephalotaxine (1b), has been developed on the basis of the key intramolecular Schmidt reaction of symmetric azido-diones 5 and 18, respectively.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19320459     DOI: 10.1021/jo900113s

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  3 in total

1.  Overcoming product inhibition in catalysis of the intramolecular Schmidt reaction.

Authors:  Hashim F Motiwala; Charlie Fehl; Sze-Wan Li; Erin Hirt; Patrick Porubsky; Jeffrey Aubé
Journal:  J Am Chem Soc       Date:  2013-06-07       Impact factor: 15.419

2.  Synthesis of medium-bridged twisted lactams via cation-pi control of the regiochemistry of the intramolecular Schmidt reaction.

Authors:  Michal Szostak; Lei Yao; Jeffrey Aubé
Journal:  J Org Chem       Date:  2010-02-19       Impact factor: 4.354

Review 3.  Cephalotaxus Alkaloids.

Authors:  Joëlle Pérard-Viret; Laith Quteishat; Rana Alsalim; Jacques Royer; Françoise Dumas
Journal:  Alkaloids Chem Biol       Date:  2017-08-16
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.