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Titolo:
Enantioselective inclusion in bile acids: resolution of cyclic ketones
Autore:
Bertolasi, V; Bortolini, O; Fogagnolo, M; Fantin, G; Pedrini, P;
Indirizzi:
Univ Ferrara, Dipartimento Chim, I-44100 Ferrara, Italy Univ Ferrara Ferrara Italy I-44100 rtimento Chim, I-44100 Ferrara, Italy
Titolo Testata:
TETRAHEDRON-ASYMMETRY
fascicolo: 10, volume: 12, anno: 2001,
pagine: 1479 - 1483
SICI:
0957-4166(20010622)12:10<1479:EIIBAR>2.0.ZU;2-M
Fonte:
ISI
Lingua:
ENG
Soggetto:
EFFICIENT OPTICAL RESOLUTION; CHOLIC-ACID; ALIPHATIC-ALCOHOLS; CRYSTAL-STRUCTURES; COMPLEXATION; SULFOXIDES; COMPOUND;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Physical, Chemical & Earth Sciences
Citazioni:
35
Recensione:
Indirizzi per estratti:
Indirizzo: Fantin, G Univ Ferrara, Dipartimento Chim, Via Borsari 46, I-44100 Ferrara, Italy Univ Ferrara Via Borsari 46 Ferrara Italy I-44100 errara, Italy
Citazione:
V. Bertolasi et al., "Enantioselective inclusion in bile acids: resolution of cyclic ketones", TETRAHEDR-A, 12(10), 2001, pp. 1479-1483

Abstract

Cholic and deoxycholic acids were found to form inclusion compounds with various racemic cyclic ketones enabling direct and straightforward enantiomer separation. The X-ray structure of the 2:1 inclusion complex between (-)-bicyclo[3.2.0]-hept-2-en-6-one and cholic acid is reported. (C) 2001 Elsevier Science Ltd. All rights reserved.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 02/04/20 alle ore 18:03:13