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
Authors:
- 1 March 2003
- journal article
- research article
- Published by SAGE Publications in Journal of Chemical Research
- Vol. 2003 (3) , 117-120
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 systemsKeywords
This publication has 7 references indexed in Scilit:
- Synthesis and in vitro anticancer activity evaluation of biscarbamic esters of 2,3-bis (hydroxymethyl)-1-methyl-7- and 7,8 -substituted-benzo[g]indolesIl Farmaco, 1998
- Regioselective Synthesis of Several Heterocyclic Fused Azepines Using Diisobutylaluminum HydrideHETEROCYCLES, 1998
- Triphenylphosphine Catalyzed Stereoselective Synthesis ofO-VinyloximesSynthetic Communications, 1997
- A Facile Synthesis of 4-Oxo-4,5,6,7-tetrahydroindolesHETEROCYCLES, 1984
- Reactions of Acetylenecarboxylic Esters with Nitrogen-Containing Heterocycles1979
- Nuclear magnetic resonance spectroscopy. Use of carbon-13 spectra to establish configurations of oximesThe Journal of Organic Chemistry, 1974
- Herstellung und Eigenschaften von Oximen des 4‐Oxo‐4,5,6,7‐tetrahydroindols und ihre Umlagerung in Pyrrolo‐azepine 6. Mitteilung über synthetische Indol‐Verbindungen [1]Helvetica Chimica Acta, 1968