A POSSIBLE PATHWAY FOR THE REACTION OF TRIETHYL (1-METHYLINDOL-2-YL)BORATE WITH CATIONIC ELECTROPHILES IN THE PRESENCE OF CUPROUS CYANIDE

Authors
ISHIKURA M TERASHIMA M
Citation
M. Ishikura et M. Terashima, A POSSIBLE PATHWAY FOR THE REACTION OF TRIETHYL (1-METHYLINDOL-2-YL)BORATE WITH CATIONIC ELECTROPHILES IN THE PRESENCE OF CUPROUS CYANIDE, Journal of heterocyclic chemistry, 31(4), 1994, pp. 977-980
Citations number
17
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Journal of heterocyclic chemistry → ACNP
ISSN journal
0022152X
Volume
31
Issue
4
Year of publication
1994
Pages
977 - 980
Database
ISI
SICI code
0022-152X(1994)31:4<977:APPFTR>2.0.ZU;2-F
Abstract
On the preferential formation of 3-substituted indoles from triethyl ( 1-methylindol-2-yl)borate in the presence of cuprous cyanide and catio nic electrophiles, it was supposed that the reaction seems to proceed through a transposition path from boron to copper.