thermal rearrangement of 6,7-dihydrobenzo[b]furan-4(5H)-one and 4,5,6,7-tetrahydroindol-4-one 4(7)-O-(E)-(1.2-dimethoxycarbonylvinyl)ketoximes gave 4,5-dihydrofuro[2,3g]- and 4,5-dihidropyrrolo[2,3g]- and [3,2-g] indoles, three novel tricyclic systems

Addition reactions of acetylenic esters to 6,7-dihydrobenzo[b]furan-4-(5H)-one, 6,7-dihydroindol-4(5H)-one, 5,6-dihydrobenzo[b]furan-7(6H)-one and 5,6-dihydroindol-7(6H)-one ketoximes. Formation of reduced furo[g]- and pyrrole[g]indoles / Pinna, Gerard Aime; Sechi, Mario; Paglietti, Giuseppe; Pirisi, Maria Antonietta. - In: JOURNAL OF CHEMICAL RESEARCH. SYNOPSES. - ISSN 0308-2342. - 2003:3(2003), pp. 117-120. [10.3184/030823403103173426]

Addition reactions of acetylenic esters to 6,7-dihydrobenzo[b]furan-4-(5H)-one, 6,7-dihydroindol-4(5H)-one, 5,6-dihydrobenzo[b]furan-7(6H)-one and 5,6-dihydroindol-7(6H)-one ketoximes. Formation of reduced furo[g]- and pyrrole[g]indoles

PINNA, Gerard Aime;SECHI MARIO;PIRISI, Maria Antonietta
2003

Abstract

thermal rearrangement of 6,7-dihydrobenzo[b]furan-4(5H)-one and 4,5,6,7-tetrahydroindol-4-one 4(7)-O-(E)-(1.2-dimethoxycarbonylvinyl)ketoximes gave 4,5-dihydrofuro[2,3g]- and 4,5-dihidropyrrolo[2,3g]- and [3,2-g] indoles, three novel tricyclic systems
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/11388/82462
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