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Titolo:
REGIO AND STEREOSELECTIVE FORMATION OF DIHYDROFURANS BY CERIC AMMONIUM-NITRATE MEDIATED OXIDATIVE [3-DIKETONES TO CINNAMIC ESTERS(2] CYCLOADDITION OF 1,3)
Autore:
ROY SC; MANDAL PK;
Indirizzi:
INDIAN ASSOC CULTIVAT SCI,DEPT ORGAN CHEM CALCUTTA 700032 W BENGAL INDIA
Titolo Testata:
Tetrahedron
fascicolo: 6, volume: 52, anno: 1996,
pagine: 2193 - 2198
SICI:
0040-4020(1996)52:6<2193:RASFOD>2.0.ZU;2-0
Fonte:
ISI
Lingua:
ENG
Soggetto:
TRIMETHYLSILYL ENOL ETHERS; 1,3-DICARBONYL COMPOUNDS; ORGANIC-SYNTHESIS; FREE-RADICALS; METAL-SALTS; CERIUM(IV); VINYL; MANGANESE(III); ACETATE; ALKENES;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Science Citation Index Expanded
Citazioni:
23
Recensione:
Indirizzi per estratti:
Citazione:
S.C. Roy e P.K. Mandal, "REGIO AND STEREOSELECTIVE FORMATION OF DIHYDROFURANS BY CERIC AMMONIUM-NITRATE MEDIATED OXIDATIVE [3-DIKETONES TO CINNAMIC ESTERS(2] CYCLOADDITION OF 1,3)", Tetrahedron, 52(6), 1996, pp. 2193-2198

Abstract

Regio and stereoselective syntheses of dihydrofurans were accomplished by eerie ammonium nitrate mediated oxidative [3+2] cycloaddition of 1,3-diketones to cinnamic esters in high yield.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 01/12/20 alle ore 01:16:44