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Titolo:
A convergent strategy for the synthesis of beta-carba-galacto-disaccharides
Autore:
Cheng, XH; Khan, N; Kumaran, G; Mootoo, DR;
Indirizzi:
CUNY Hunter Coll, Dept Chem, New York, NY 10021 USA CUNY Hunter Coll New York NY USA 10021 Dept Chem, New York, NY 10021 USA
Titolo Testata:
ORGANIC LETTERS
fascicolo: 9, volume: 3, anno: 2001,
pagine: 1323 - 1325
SICI:
1523-7060(20010503)3:9<1323:ACSFTS>2.0.ZU;2-G
Fonte:
ISI
Lingua:
ENG
Soggetto:
SIALYL-LEWIS-X; C-GLYCOSIDES; BINDING; CONFORMATION; LACTOSE; MONOSACCHARIDES; ESTERIFICATION; RECOGNITION; INHIBITORS; ACETALS;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Physical, Chemical & Earth Sciences
Citazioni:
44
Recensione:
Indirizzi per estratti:
Indirizzo: Mootoo, DR CUNY Hunter Coll, Dept Chem, 695 Pk Ave, New York, NY 10021 USACUNY Hunter Coll 695 Pk Ave New York NY USA 10021 NY 10021 USA
Citazione:
X.H. Cheng et al., "A convergent strategy for the synthesis of beta-carba-galacto-disaccharides", ORG LETT, 3(9), 2001, pp. 1323-1325

Abstract

[GRAPHICS]A convergent strategy for the synthesis of beta -carba-galacto-disaccharides is illustrated by the preparation of 1 and 4, from a central "glycone" component 22, and the corresponding "aglycone" segments, monosaccharide alcohols, 23a or 23b, The key step is the formation of the carbasugar ring via an oxocarbenium ion-enol ether cyclization.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 28/09/20 alle ore 18:10:29