Literature DB >> 23639065

SmI2-mediated couplings of α-amino acid derivatives. Formal synthesis of (-)-pumiliotoxin 251D and (±)-epiquinamide.

Vagner D Pinho1, David J Procter, Antonio C B Burtoloso.   

Abstract

The coupling between cyclic and acyclic α-amino acid derivatives and methyl acrylate, mediated by samarium diiodide, is described. The method constitutes a powerful tool to construct indolizidine, quinolizidine, and piperidine systems in a straightforward two-step fashion. The formal synthesis of (-)-pumiliotoxin 251D and (±)-epiquinamide is achieved after two or three steps from these amino acid derivatives.

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Year:  2013        PMID: 23639065     DOI: 10.1021/ol400903n

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


  3 in total

1.  Towards stereochemical control: A short formal enantioselective total synthesis of pumiliotoxins 251D and 237A.

Authors:  Jie Zhang; Hong-Kui Zhang; Pei-Qiang Huang
Journal:  Beilstein J Org Chem       Date:  2013-11-05       Impact factor: 2.883

2.  Decarboxylative Annulation of α-Amino Acids with γ-Nitroaldehydes.

Authors:  YoungKu Kang; Daniel Seidel
Journal:  Org Lett       Date:  2016-08-10       Impact factor: 6.005

Review 3.  Synthesis of Nitrogen Heterocycles Using Samarium(II) Iodide.

Authors:  Shicheng Shi; Michal Szostak
Journal:  Molecules       Date:  2017-11-21       Impact factor: 4.411

  3 in total

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