Syntheses of N-substituted 3,3,4-triaryl- and 3,3,4,4-tetraphenyl-2-azetidinones.

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概要

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• The reactions of 2-diazo-1,2-diphenylethanone with Schiff's bases Ar–CH=N–R gave new substituted 2-azetidinones together with 1,1′,4,4′-tetraphenyl-2,2′-azinodiethanone. 2-Diazo-1,2-diphenylethanone reacts with <I>N</I>-benzhydrylidene-<I>N</I>′-phenylurea to give 1-(phenylcarbamoyl)-3,3,4,4-tetraphenyl-2-azetidinone.

• 公益社団法人 日本化学会の論文

著者

• Singh Surendra

  Department of Chemistry, Banaras Hindu University

• Mehrotra Kailash

  Department of Chemistry, Banaras Hindu University

関連論文

• PROJECTIVE CURVATURE INHERITANCE IN FINSLER SPACES II
• Syntheses of N-substituted 3,3,4-triaryl- and 3,3,4,4-tetraphenyl-2-azetidinones.
• ON THE CURVATURE INHERITANCE IN FINSLER SPACE
• Novel and convenient synthesis of dioxaphospholes.
• Photochemical transformations of 1,2-diketones and benzhydrylamine.
• Reaction between azibenzil and diarylmethanimine.
• Cyclizations of dianions from 2-imino-1,2-diphenylethanone to oxazolines, oxazocines, and oxazonines.

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