A novel tryptophan dioxygenation by Superoxide

DOI: 10.1016/S0040-4039(00)92244-5

Source and publish data:

Tetrahedron Letters p. 2567 - 2570 (1992)

Update date:2022-08-06

Topics:

Authors:

Itakura, Koichi

Uchida, Koji

Kawakishi, Shunro

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Article abstract of DOI:10.1016/S0040-4039(00)92244-5

The reactions of N-acyl-L-tryptophans, (1) and (2, with O₂^- afforded their corresponding 2,3-bond cleavage compounds, (5) and (7), as the major products. On the other hand, the reactions of N-acyl-L-tryptophan alkylamides, (3) and (4

Full text of DOI:10.1016/S0040-4039(00)92244-5

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