Literature DB >> 21291173

Ag(I)-catalyzed regioselective ring-opening of N-tosylaziridine and N-tosylazetidine with S-, O-, and N-nucleophiles and tethered dinucleophiles.

Milan Bera1, Sanjay Pratihar, Sujit Roy.   

Abstract

[Ag(COD)(2)]PF(6) catalyzes the ring-opening of N-tosylaziridines and -azetidines with alcohols, amines, thiols, and related tethered 1,2-ethane dinucleophiles. Initial rate studies and DFT-based evaluation of stepwise energetics suggest an inverse relationship between the nucleophilic reactivity of a heteroatom donor and its binding affinity to cationic Ag(I).

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Year:  2011        PMID: 21291173     DOI: 10.1021/jo102285z

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


  3 in total

1.  A specific nucleophilic ring-opening reaction of aziridines as a unique platform for the construction of hydrogen polysulfides sensors.

Authors:  Wei Chen; Ethan W Rosser; Di Zhang; Wen Shi; Yilin Li; Wen-Ji Dong; Huimin Ma; Dehong Hu; Ming Xian
Journal:  Org Lett       Date:  2015-05-11       Impact factor: 6.005

2.  Synthesis of β-alkoxy-N-protected phenethylamines via one-pot copper-catalyzed aziridination and ring opening.

Authors:  Jorge Saavedra-Olavarría; Matías Madrid-Rojas; Iriux Almodovar; Patricio Hermosilla-Ibáñez; Edwin G Pérez
Journal:  RSC Adv       Date:  2018-08-06       Impact factor: 4.036

3.  Synthesis of cis-C-iodo-N-tosyl-aziridines using diiodomethyllithium: reaction optimization, product scope and stability, and a protocol for selection of stationary phase for chromatography.

Authors:  Tom Boultwood; Dominic P Affron; Aaron D Trowbridge; James A Bull
Journal:  J Org Chem       Date:  2013-06-18       Impact factor: 4.354

  3 in total

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