Reaction of methiodides of 1,2,3,4-tetrahydro-γ-carbolines with nucleophilic agents

DOI: 10.1007/BF00503661

Source and publish data:

Chemistry of Heterocyclic Compounds p. 794 - 800 (1982)

Update date:2022-08-04

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Authors:

Yurovskaya

Rodionov

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Article abstract of DOI:10.1007/BF00503661

It is shown that C, N, and O nucleophiles smoothly cleave the hydrogenated ring of quaternized tetrahydro-γ-carbolines to give isotryptamine derivatives with a CH₂Z substituent in the 3 position (Z = Me, Ph, CN, OEt, piperidino, and morpholino)

Full text of DOI:10.1007/BF00503661

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