Cleavage of some annulated tetrahydropyridines under the action of dimethyl acetylene dicarboxylate in protic solvents. New practical route to substituted pyrroles and indoles

Tetrahydropyrrolo[3,2-c]pyridines and tetrahydropyrido[4,3-b]indoles undergo piperidine ring opening under the action of dimethyl acetylene dicarboxylate in alcohols or in aqueous dioxane, providing β -(alk)oxy-substituted pyrroles (indoles) in moderate to high yields.

Publisher
SPRINGER
Number of issue
3-4
Language
English
Pages
207-212
Status
Published
Volume
6
Year
2003
Organizations
  • 1 Organic Chemistry Department, Russ. Peoples Friendship University, 6, Miklukho-Maklaya St., Moscow, 117198, Russian Federation
Keywords
Cleavage; Indole; Pyridines; Pyrrole; Tandem reactions
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Other records

Sheka E.F.
Lecture Notes in Computer Science (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). Vol. 2658. 2003. P. 386-403