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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 pyrrolo[g]-indoles

Pinna, Gérard Aimé and Sechi, Mario and Paglietti, Giuseppe and Pirisi, Maria Antonietta (2003) 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 pyrrolo[g]-indoles. Journal of Chemical Research, Vol. 3 , p. 117-120. ISSN 0308-2342. Article.

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DOI: 10.3184/030823403103173426

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-dihydropyrrolo[2,3g]- and [3,2-g] indoles, three novel tricyclic systems

Item Type:Article
ID Code:547
Status:Published
Refereed:Yes
Uncontrolled Keywords:Michael reactions, acetylenic esters, thermal aza-Cope rearrangement
Subjects:Area 03 - Scienze chimiche > CHIM/08 Chimica farmaceutica
Divisions:001 Università di Sassari > 01 Dipartimenti > Farmaco, chimico, tossicologico
Publisher:Science Reviews 2000
ISSN:0308-2342
Deposited On:18 Aug 2009 10:02

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