Catalogo Articoli (Spogli Riviste)

OPAC HELP

Titolo:
The first total synthesis of (-)-solanapyrone E based on domino Michael strategy
Autore:
Hagiwara, H; Kobayashi, K; Miya, S; Hoshi, T; Suzuki, T; Ando, M;
Indirizzi:
Niigata Univ, Grad Sch Sci & Technol, Niigata 9502181, Japan Niigata UnivNiigata Japan 9502181 Sci & Technol, Niigata 9502181, Japan Niigata Univ, Fac Engn, Niigata 9502181, Japan Niigata Univ Niigata Japan 9502181 niv, Fac Engn, Niigata 9502181, Japan
Titolo Testata:
ORGANIC LETTERS
fascicolo: 2, volume: 3, anno: 2001,
pagine: 251 - 254
SICI:
1523-7060(20010125)3:2<251:TFTSO(>2.0.ZU;2-9
Fonte:
ISI
Lingua:
ENG
Soggetto:
DIELS-ALDER REACTION; SOLANAPYRONES; BIOSYNTHESIS;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Physical, Chemical & Earth Sciences
Citazioni:
13
Recensione:
Indirizzi per estratti:
Indirizzo: Hagiwara, H Niigata Univ, Grad Sch Sci & Technol, 8050 2 Nocho, Niigata 9502181, Japan Niigata Univ 8050 2 Nocho Niigata Japan 9502181 502181, Japan
Citazione:
H. Hagiwara et al., "The first total synthesis of (-)-solanapyrone E based on domino Michael strategy", ORG LETT, 3(2), 2001, pp. 251-254

Abstract

[GRAPHICS]A phytotoxin, solanapyrone E, has been synthesized from the decalone prepared by the domino Michael reaction of the kinetic enolate of optically pureacetylcyclohexene with methyl crotonate, After several transformations on the decalone ring, condensation of a methyl acetoacetate equivalent installed a pyrone moiety and introduction of a hydroxymethyl unit into the pyronering furnished solanapyrone E.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 28/01/20 alle ore 14:39:52