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Titolo:
A rhodium carbene cyclization-cycloaddition cascade strategy toward the pseudolaric acids
Autore:
Chiu, P; Chen, B; Cheng, KF;
Indirizzi:
Univ Hong Kong, Dept Chem, Hong Kong, Hong Kong, Peoples R China Univ HongKong Hong Kong Hong Kong Peoples R China Kong, Peoples R China
Titolo Testata:
ORGANIC LETTERS
fascicolo: 11, volume: 3, anno: 2001,
pagine: 1721 - 1724
SICI:
1523-7060(20010531)3:11<1721:ARCCCS>2.0.ZU;2-D
Fonte:
ISI
Lingua:
ENG
Soggetto:
CARBONYL YLIDE FORMATION; ANTIBIOTIC X-206; KAEMPFERI; DERIVATIVES; CATALYST; KETONES; ESTERS; LIGAND;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Physical, Chemical & Earth Sciences
Citazioni:
32
Recensione:
Indirizzi per estratti:
Indirizzo: Chiu, P Univ Hong Kong, Dept Chem, Pokfulam Rd, Hong Kong, Hong Kong, Peoples R China Univ Hong Kong Pokfulam Rd Hong Kong Hong Kong Peoples R Chinana
Citazione:
P. Chiu et al., "A rhodium carbene cyclization-cycloaddition cascade strategy toward the pseudolaric acids", ORG LETT, 3(11), 2001, pp. 1721-1724

Abstract

A rhodium carbene intramolecular cyclization-cycloaddition cascade was employed as the key reaction in the synthesis of the nucleus of the cytotoxic diterpenoids pseudolaric acids A and B.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 30/09/20 alle ore 00:01:02