REGIO-CONTROLLED CYCLIZATION OF 1-(3-METHYL-2-BUTENOYL)INDOLES AT THEIR 2-POSITIONS AND 7-POSITIONS

Authors
NAKATSUKA S HU DY TANAHASHI M
Citation
S. Nakatsuka et al., REGIO-CONTROLLED CYCLIZATION OF 1-(3-METHYL-2-BUTENOYL)INDOLES AT THEIR 2-POSITIONS AND 7-POSITIONS, Heterocyclic communications, 2(6), 1996, pp. 555-558
Citations number
17
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Heterocyclic communications → ACNP
ISSN journal
07930283
Volume
2
Issue
6
Year of publication
1996
Pages
555 - 558
Database
ISI
SICI code
0793-0283(1996)2:6<555:RCO1AT>2.0.ZU;2-1
Abstract
A quarternary carbon substituent was efficiently introduced at their 2 and 7-positions of the indole nucleus by cyclization of 1-(3-methyl-2 -butenoyl)-indole derivatives 4 and 7, and derived to a reversed preny l group found in teleocidins 3 or echinulin 11.