Literature DB >> 14627395

A new, mild synthesis of N-sulfonyl ketimines via the palladium-catalyzed isomerization of aziridines.

John P Wolfe1, Joshua E Ney.   

Abstract

[reaction: see text] A new method for the synthesis of N-tosylketimines via the palladium-catalyzed isomerization of N-tosylaziridines is described. The mild reaction conditions tolerate the presence of a variety of functional groups including ketones, esters, and acetals. The reactions are believed to proceed via the oxidative addition of the aziridine to Pd(0) and represent the first examples of transformations involving Pd(0)-mediated oxidative additions of aziridines that do not proceed through allylpalladium intermediates.

Entities:  

Year:  2003        PMID: 14627395     DOI: 10.1021/ol0357651

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


  4 in total

1.  Asymmetric synthesis via stereospecific C-N and C-O bond activation of alkyl amine and alcohol derivatives.

Authors:  Sarah M Pound; Mary P Watson
Journal:  Chem Commun (Camb)       Date:  2018-10-30       Impact factor: 6.222

2.  Coupling of Vinyl Aziridines and Isocyanates.

Authors:  Kainan Zhang; Pramod R Chopade; Janis Louie
Journal:  Tetrahedron Lett       Date:  2008       Impact factor: 2.415

3.  Catalyst-controlled regiodivergent ring-opening C(sp3)-Si bond-forming reactions of 2-arylaziridines with silylborane enabled by synergistic palladium/copper dual catalysis.

Authors:  Youhei Takeda; Kaoru Shibuta; Shohei Aoki; Norimitsu Tohnai; Satoshi Minakata
Journal:  Chem Sci       Date:  2019-07-31       Impact factor: 9.825

4.  Palladium-catalyzed regioselective and stereo-invertive ring-opening borylation of 2-arylaziridines with bis(pinacolato)diboron: experimental and computational studies.

Authors:  Youhei Takeda; Akinobu Kuroda; W M C Sameera; Keiji Morokuma; Satoshi Minakata
Journal:  Chem Sci       Date:  2016-06-09       Impact factor: 9.825

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.