Literature DB >> 10891139

Preparation of 1,5-disubstituted pyrrolidin-2-ones.

A R Katritzky1, S Mehta, H Y He, X Cui.   

Abstract

1,5-Disubstituted pyrrolidin-2-ones 18a-g, 19a-h, and 20a-f were synthesized in good to excellent yields via the nucleophilic substitution of 5-(benzotriazol-1-yl)-1-substituted-pyrrolidin-2-ones 9 with allylsilanes, organozinc reagents, and phosphorus compounds. Compounds 9 and 5-(benzotriazol-2-yl)-1-substituted-pyrrolidin-2-one isomers 10 are readily prepared in total 70-84% yields from 2, 5-dimethoxy-2,5-dihydrofuran (7), primary amines 8, and benzotriazole; 9 and 10 react identically with nucleophiles.

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Year:  2000        PMID: 10891139     DOI: 10.1021/jo000219w

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


  1 in total

1.  Green synthesis of new chiral 1-(arylamino)imidazo[2,1-a]isoindole-2,5-diones from the corresponding α-amino acid arylhydrazides in aqueous medium.

Authors:  Nadia Bouzayani; Jamil Kraїem; Sylvain Marque; Yakdhane Kacem; Abel Carlin-Sinclair; Jérôme Marrot; Béchir Ben Hassine
Journal:  Beilstein J Org Chem       Date:  2018-11-26       Impact factor: 2.883

  1 in total

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