Regioselective nitration of 1-acyl-4-methoxyindolines leads to efficient synthesis of a photolabile L-glutamate precursor
Regioselective nitration of 1-acyl-4-methoxyindolines leads to efficient synthesis of a photolabile L-glutamate precursor
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DOI:
10.1081/scc-120004148
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发表时间:
2002-01-01
影响因子:
2.1
通讯作者:
Corrie, JET
中科院分区:
文献类型:
--
作者:
Papageorgiou, G;Corrie, JET
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.