FACILE SYNTHESIS OF THE KEY INTERMEDIATE OF EO-9 VIA THE FORMATION OFTHE INDOLE SKELETON USING THE NENITZESCU REACTION

Authors
KINUGAWA M ARAI H NISHIKAWA H SAKAGUCHI A OGASA T TOMIOKA S KASAI M
Citation
M. Kinugawa et al., FACILE SYNTHESIS OF THE KEY INTERMEDIATE OF EO-9 VIA THE FORMATION OFTHE INDOLE SKELETON USING THE NENITZESCU REACTION, Journal of the Chemical Society. Perkin transactions. I, (21), 1995, pp. 2677-2678
Citations number
10
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Journal of the Chemical Society. Perkin transactions. I → ACNP
ISSN journal
0300922X
Issue
21
Year of publication
1995
Pages
2677 - 2678
Database
ISI
SICI code
0300-922X(1995):21<2677:FSOTKI>2.0.ZU;2-C
Abstract
A Nenitzescu reaction has been used to prepare the indole skeleton 6 h aving all the functional groups necessary for its conversion into 10a, a key intermediate in a short synthesis of the indolequinone EO 9.