PHOTOLYSIS OF PHENYLTELLUROTRIFLUOROACETIMIDATES - A NEW APPROACH TO GENERATION OF ALPHA-TRIFLUOROACETIMIDOYL RADICALS LEADING TO THE SYNTHESIS OF INDOLE-DERIVATIVES

Authors
UEDA Y WATANABE H UEMURA J UNEYAMA K
Citation
Y. Ueda et al., PHOTOLYSIS OF PHENYLTELLUROTRIFLUOROACETIMIDATES - A NEW APPROACH TO GENERATION OF ALPHA-TRIFLUOROACETIMIDOYL RADICALS LEADING TO THE SYNTHESIS OF INDOLE-DERIVATIVES, Tetrahedron letters, 34(49), 1993, pp. 7933-7934
Citations number
19
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
34
Issue
49
Year of publication
1993
Pages
7933 - 7934
Database
ISI
SICI code
0040-4039(1993)34:49<7933:POP-AN>2.0.ZU;2-W
Abstract
Photolysis of N-aryl phenyltellurotrifluoroacetimidates generates N-ar yl trifluoroacetimidoyl radicals, which undergo an intramolecular exo- attack to carbon-carbon triple bond leading to indole derivatives.