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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.

✍ Scribed by Gerard Aime Pinna; Mario Sechi; Giuseppe Paglietti; Maria Antonietta Pirisi


Publisher
John Wiley and Sons
Year
2003
Weight
118 KB
Volume
34
Category
Article
ISSN
0931-7597

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✦ Synopsis


Abstract

For Abstract see ChemInform Abstract in Full Text.


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✍ B. Joseph; O. Cornec; J.-Y. Mérour; X. Solans; M. Font-Bardia 📂 Article 📅 1997 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 539 KB

## Abstract The synthetic routes of 6,7‐dihydrobenzo[4,5]cyclohept[1,2‐__b__]indol‐12(5__H__)‐one 5 from either 1‐methyl or 1‐sulfonylindole‐2‐carboxaldehyde 1 or ethyl 1,2‐dimethylindole‐3‐carboxylate 6 are reported. The structure of the ketone 5a was confirmed by X‐ray crystallography. Several in