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-Reference-Cited by-同舟云学术

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

Published:2003-03 Issue:3 Volume:2003 Page:117-120
ISSN:1747-5198
Container-title:Journal of Chemical Research
language:en
Short-container-title:Journal of Chemical Research

Author:

Pinna Gérard Aimè¹,Sechi Mario¹,Paglietti Giuseppe¹,Pirisi Maria Antonietta¹

Affiliation:

1. Dipartimento Farmacochimico Tossicologico, University of Sassari, Via Muroni 23/A, 07100 Sassari, Italy

Abstract

Thermal rearrangement of 6,7-dihydrobenzo[ b]furan-4(5 H)-one and 4,5,6,7-tetrahydroindol-4-one 4(7)- O-( E)-(1,2-dimethoxycarbonylvinyl)ketoximes gave 4,5-dihydrofuro[2,3 g]- and 4,5-dihydropyrrolo[2,3 g]- and [3,2- g] indoles, three novel tricyclic systems

Publisher

SAGE Publications

Subject

General Chemistry

Link

http://journals.sagepub.com/doi/pdf/10.3184/030823403103173426

Reference12 articles.

1. Synthesis and in vitro anticancer activity evaluation of biscarbamic esters of 2,3-bis (hydroxymethyl)-1-methyl-7- and 7,8 -substituted-benzo[g]indoles

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