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2002 amino acids, peptides amino acids, peptides U 0400 40 - 196 Regioselective Nitration of 1-Acyl-4-methoxyindolines Leads to Efficient Synthesis of a Photolabile L-Glutamate Precursor. Selective nitration of the title indoline (I) in 7-position can be achieved by using Claycop as the nitrating agent. — (PAPAGEORGIOU, GEORGE; CORRIE, JOHN E. T.; Synth. Commun. 32 (2002) 10, 1571-1577; Natl. Inst. Med. Res., London NW7 1AA, UK; EN) 1

Regioselective Nitration of 1-Acyl-4-methoxyindolines Leads to Efficient Synthesis of a Photolabile L-Glutamate Precursor

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Page 1: Regioselective Nitration of 1-Acyl-4-methoxyindolines Leads to Efficient Synthesis of a Photolabile L-Glutamate Precursor

2002 amino acids, peptides

amino acids, peptidesU 0400

40 - 196Regioselective Nitration of 1-Acyl-4-methoxyindolines Leads toEfficient Synthesis of a Photolabile L-Glutamate Precursor. —Selective nitration of the title indoline (I) in 7-position can be achieved by usingClaycop as the nitrating agent. — (PAPAGEORGIOU, GEORGE; CORRIE,JOHN E. T.; Synth. Commun. 32 (2002) 10, 1571-1577; Natl. Inst. Med. Res.,London NW7 1AA, UK; EN)

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