The Journal of organic chemistry

Diastereoselective synthesis of structurally and stereochemically diversified 2-oxa-7-azabicyclo [4.1. 0] hept-3-enyl carboxylates and their potential application …

P Mukherjee, AR Das

Index: Pal, Gargi; Paul, Sanjay; Ghosh, Partha Pratim; Das, Asish R. RSC Advances, 2014 , vol. 4, # 16 p. 8300 - 8307

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Abstract

An advanced protocol for the diastereoselective intramolecular aziridination reaction has been developed to synthesize 2-oxa-7-azabicyclo [4.1. 0] hept-3-en-1-yl carboxylate from their corresponding 4-H-pyrans and spiropyrans analogues employing iodosylbenznene as

~92%

~83%

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