Facile Synthesis of Oxime Amino Ethers via Lewis Acid Catalyzed SN2-Type Ring Opening of Activated Aziridines with Aryl Aldehyde Oximes

Bhattacharyya, Aditya ; Das, Subhomoy ; Chauhan, Navya ; Biswas, Pronay K. ; Ghorai, Manas K. (2020) Facile Synthesis of Oxime Amino Ethers via Lewis Acid Catalyzed SN2-Type Ring Opening of Activated Aziridines with Aryl Aldehyde Oximes Synlett, 31 (07). pp. 708-712. ISSN 0936-5214

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Official URL: http://doi.org/10.1055/s-0039-1691596

Related URL: http://dx.doi.org/10.1055/s-0039-1691596

Abstract

A simple strategy to access a wide range of substituted oxime amino ethers in good to high yields via Lewis acid catalyzed SN2-type ring opening of activated aziridines with aryl aldehyde oximes is reported.

Item Type:Article
Source:Copyright of this article belongs to Georg Thieme Verlag KG.
Keywords:Azaheterocycles; Aziridine; Azirine; Domino Ring-opening Cyclization; Intramolecular Cyclization; Ring-expansion; Ring-opening; Sn2 Type Reaction.
ID Code:117078
Deposited On:15 Apr 2021 07:40
Last Modified:15 Apr 2021 07:40

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