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Titolo:
1,2-epimino-3,4-epoxybutane: A versatile chiral building block
Autore:
Harms, G; Schaumann, E; Adiwidjaja, G;
Indirizzi:
Tech Univ Clausthal, Inst Organ Chem, D-38678 Clausthal Zellerfeld, Germany Tech Univ Clausthal Clausthal Zellerfeld Germany D-38678 erfeld, Germany Univ Hamburg, Mineral Petrog Inst, D-20146 Hamburg, Germany Univ Hamburg Hamburg Germany D-20146 trog Inst, D-20146 Hamburg, Germany
Titolo Testata:
SYNTHESIS-STUTTGART
fascicolo: 4, , anno: 2001,
pagine: 577 - 580
SICI:
0039-7881(200104):4<577:1AVCBB>2.0.ZU;2-7
Fonte:
ISI
Lingua:
ENG
Soggetto:
ASYMMETRIC AMINOHYDROXYLATION; AMINO-ACIDS; ALCOHOLS; ACCESS;
Keywords:
amino alcohols; domino reactions; epoxides; ring opening; cyclopentanes;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Life Sciences
Physical, Chemical & Earth Sciences
Citazioni:
16
Recensione:
Indirizzi per estratti:
Indirizzo: Schaumann, E Tech Univ Clausthal, Inst Organ Chem, Leibnizstr 6, D-38678 Clausthal Zellerfeld, Germany Tech Univ Clausthal Leibnizstr 6 Clausthal Zellerfeld Germany D-38678
Citazione:
G. Harms et al., "1,2-epimino-3,4-epoxybutane: A versatile chiral building block", SYNTHESIS-S, (4), 2001, pp. 577-580

Abstract

The synthesis of enantiomerically pure 1,2-epimino-3,4-epoxy-(N-toluenesulfonyl)butane (6) in the S,R-(erythro) and R,R-(threo) configurations is described. This building block offers a new route to targets with an 1,2-aminohydroxy functionality. As an example, the new 1,4-biselectrophile is employed in a cyclopentane synthesis.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 28/09/20 alle ore 18:38:09