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Titolo:
Interesting stereoselectivity of intramolecular Diels-Alder reactions leading to 5-carbomethoxy yohimbine systems
Autore:
Leonard, J; Hague, AB; Harms, G; Jones, ME;
Indirizzi:
Univ Salford, Dept Chem, Salford M5 4WT, Lancs, England Univ Salford Salford Lancs England M5 4WT Salford M5 4WT, Lancs, England Glaxo Wellcome Res & Dev Ltd, Chem Dev, Stevenage SG1 2NY, Herts, England Glaxo Wellcome Res & Dev Ltd Stevenage Herts England SG1 2NY rts, England
Titolo Testata:
TETRAHEDRON LETTERS
fascicolo: 46, volume: 40, anno: 1999,
pagine: 8141 - 8145
SICI:
0040-4039(19991112)40:46<8141:ISOIDR>2.0.ZU;2-F
Fonte:
ISI
Lingua:
ENG
Soggetto:
INDOLE ALKALOIDS; MANZAMINE-A; BICYCLOANNULATION; DIENES; BONDS;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Life Sciences
Physical, Chemical & Earth Sciences
Citazioni:
22
Recensione:
Indirizzi per estratti:
Indirizzo: Leonard, J Univ Salford, Dept Chem, Salford M5 4WT, Lancs, England Univ Salford Salford Lancs England M5 4WT 4WT, Lancs, England
Citazione:
J. Leonard et al., "Interesting stereoselectivity of intramolecular Diels-Alder reactions leading to 5-carbomethoxy yohimbine systems", TETRAHEDR L, 40(46), 1999, pp. 8141-8145

Abstract

5-Carboxy apoyohimbine ring systems have been prepared via intramolecular Diels-Alder reactions of systems that incorporate electron-deficient dienesand acylamide dienophiles. These mismatched systems cyclise efficiently with exo stereoselectivity. (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 28/09/20 alle ore 18:45:05