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Titolo:
Stereloselective hydrocoupling of [(1R)-exo]-3-exo-(diphenylmethyl)bornyl cinnamates by electroreduction
Autore:
Kise, N; Iwasaki, K; Tokieda, N; Ueda, N;
Indirizzi:
Tottori Univ, Fac Engn, Dept Biotechnol, Tottori 6808552, Japan Tottori Univ Tottori Japan 6808552 pt Biotechnol, Tottori 6808552, Japan
Titolo Testata:
ORGANIC LETTERS
fascicolo: 21, volume: 3, anno: 2001,
pagine: 3241 - 3244
SICI:
1523-7060(20011018)3:21<3241:SHO[C>2.0.ZU;2-J
Fonte:
ISI
Lingua:
ENG
Soggetto:
ESTERS; DERIVATIVES; REDUCTION; ALCOHOLS; ACID;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Physical, Chemical & Earth Sciences
Citazioni:
20
Recensione:
Indirizzi per estratti:
Indirizzo: Kise, N Tottori Univ, Fac Engn, Dept Biotechnol, Tottori 6808552, Japan Tottori Univ Tottori Japan 6808552 chnol, Tottori 6808552, Japan
Citazione:
N. Kise et al., "Stereloselective hydrocoupling of [(1R)-exo]-3-exo-(diphenylmethyl)bornyl cinnamates by electroreduction", ORG LETT, 3(21), 2001, pp. 3241-3244

Abstract

[GRAPHICS]The chiral auxiliary [(1R)-exo]-3-exo-(diphenylmethyl)borneol, synthesizedfrom (1R)-(+)-camphor in three steps, was highly effective for the stereoselective hydrocoupling of its cinnamates by electroreduction. From the resulting hydrodimers, (3R,4R)-3,4-diaryladipic acid esters and (3R,4R)-3,4-diarylhexane-1,6-diols were synthesized in 87-95% ee.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 26/01/20 alle ore 16:04:27