Synthesis of an indole analog of magallanesine via the [1,2]-Meisenheimer rearrangement

DOI: 10.1002/jhet.5570330658

Source and publish data:

Journal of Heterocyclic Chemistry p. 1909 - 1913 (1996)

Update date:2022-08-05

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Authors:

Yoneda, Ryuji

Kimura, Tetsuya

Kinomoto, Junko

Harusawa, Shinya

Kurihara, Takushi

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Article abstract of DOI:10.1002/jhet.5570330658

Ring expansion of azetopyridoindole 11 via the [1,2]-Meisenheimer rearrangement of the corresponding N-oxide 12 gave azocinoindole 14, which was converted into the N-benzoylenaminone 18 in 5 steps. Intramolecular cyclization of 18 was accomplished by a mo

Full text of DOI:10.1002/jhet.5570330658

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