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Titolo:
Stereoselective coupling of optically active 3-trans-cinnamoyl-2-oxazolidinones with acid anhydrides by electroreduction
Autore:
Kise, N; Hirata, Y; Hamaguchi, T; Ueda, N;
Indirizzi:
Tottori Univ, Fac Engn, Dept Biotechnol, Tottori 6800945, Japan Tottori Univ Tottori Japan 6800945 pt Biotechnol, Tottori 6800945, Japan
Titolo Testata:
TETRAHEDRON LETTERS
fascicolo: 46, volume: 40, anno: 1999,
pagine: 8125 - 8128
SICI:
0040-4039(19991112)40:46<8125:SCOOA3>2.0.ZU;2-1
Fonte:
ISI
Lingua:
ENG
Soggetto:
CHIRAL BUTENOLIDE SYNTHONS; (+)-TRANS-COGNAC LACTONE; (+)-NEPHROSTERANIC ACID; GAMMA-BUTYROLACTONES;
Keywords:
acylation; coupling reaction; electrochemistry; lactones; oxazolidinones; reduction;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Life Sciences
Physical, Chemical & Earth Sciences
Citazioni:
17
Recensione:
Indirizzi per estratti:
Indirizzo: Kise, N Tottori Univ, Fac Engn, Dept Biotechnol, Tottori 6800945, Japan Tottori Univ Tottori Japan 6800945 chnol, Tottori 6800945, Japan
Citazione:
N. Kise et al., "Stereoselective coupling of optically active 3-trans-cinnamoyl-2-oxazolidinones with acid anhydrides by electroreduction", TETRAHEDR L, 40(46), 1999, pp. 8125-8128

Abstract

The electronduction of chiral 3-trans-cinnamoyl-2-oxazolidinones with acidanhydrides gave beta-acylated products stereoselectively. The products were transformed to optically active cis-beta,gamma-disubstituted-gamma-lactones. (C) 1999 Elsevier Science Ltd. All rights reserved.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 28/01/20 alle ore 20:53:46