Synthetic communications

Regioselective nitration of 1-acyl-4-methoxyindolines leads to efficient synthesis of a photolabile L-glutamate precursor

G Papageorgiou, JET Corrie

Index: Papageorgiou, George; Corrie, John E. T. Synthetic Communications, 2002 , vol. 32, # 10 p. 1571 - 1577

Full Text: HTML

Citation Number: 18

Abstract

ABSTRACT Different nitrating reagents give different ratios of 5-and 7-nitro isomers of the title indolines. The best ratio of the 7-nitro isomer was obtained with claycop–acetic anhydride, and these conditions were particularly useful for preparation of a photolabile l- glutamate derivative.

Related Articles:

Effects of aromatic substituents on the photocleavage of 1-acyl-7-nitroindolines

[Papageorgiou, George; Corrie, John E.T Tetrahedron, 2000 , vol. 56, # 41 p. 8197 - 8205]

Effects of aromatic substituents on the photocleavage of 1-acyl-7-nitroindolines

[Papageorgiou, George; Corrie, John E.T Tetrahedron, 2000 , vol. 56, # 41 p. 8197 - 8205]

More Articles...