Literature DB >> 12098316

Diastereoselective aziridination of chiral alpha-carbonyl enoates.

Stefania Fioravanti1, Alberto Morreale, Lucio Pellacani, Paolo A Tardella.   

Abstract

Nosyloxycarbamates very efficiently aziridinate optically active alpha-carbonyl enoates with high levels of diastereoselectivity under mild conditions and in a straightforward process.

Entities:  

Year:  2002        PMID： 12098316     DOI： 10.1021/jo025670x

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


  3 in total

1.  Development of a concise synthesis of (-)-oseltamivir (Tamiflu).

Authors:  Barry M Trost; Ting Zhang
Journal:  Chemistry       Date:  2011-03-01       Impact factor: 5.236

2.  Functionalised enones as starting materials for the construction of aziridine scaffolds.

Authors:  Stefania Fioravanti; Alberto Morreale; Lucio Pellacani; Paolo A Tardella
Journal:  Mol Divers       Date:  2003       Impact factor: 2.943

3.  A practical method for the aziridination of α,β-unsaturated carbonyl compounds with a simple carbamate utilizing sodium hypochlorite pentahydrate.

Authors:  Takehiro Umeda; Satoshi Minakata
Journal:  RSC Adv       Date:  2021-06-22       Impact factor: 3.361
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.