Cyclizaticn of 3-formyl-2-acetylenylindole oximes

T. A. Prikhod'ko, S. F. Vasilevskii, M. S. Shvartsberg

Research output: Contribution to journal › Article › peer-review

Abstract

3-Formyl-2-acetylenyl-1-methylindole oximes readily undergo intramolecular heterocyclization with closure of a pyridine ring and formation of substituted γ-carboline N-oxides.

Original language	English
Pages (from-to)	2383-2385
Number of pages	3
Journal	Bulletin of the Academy of Sciences of the USSR Division of Chemical Science
Volume	33
Issue number	11
DOIs	https://doi.org/10.1007/BF00948858
Publication status	Published - 1 Nov 1984
Externally published	Yes

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Chemistry(all)

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title = "Cyclizaticn of 3-formyl-2-acetylenylindole oximes",

abstract = "3-Formyl-2-acetylenyl-1-methylindole oximes readily undergo intramolecular heterocyclization with closure of a pyridine ring and formation of substituted γ-carboline N-oxides.",

author = "Prikhod'ko, {T. A.} and Vasilevskii, {S. F.} and Shvartsberg, {M. S.}",

year = "1984",

month = nov,

day = "1",

doi = "10.1007/BF00948858",

language = "English",

volume = "33",

pages = "2383--2385",

journal = "Russian Chemical Bulletin",

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publisher = "Consultants Bureau",

number = "11",

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T1 - Cyclizaticn of 3-formyl-2-acetylenylindole oximes

AU - Prikhod'ko, T. A.

AU - Vasilevskii, S. F.

AU - Shvartsberg, M. S.

PY - 1984/11/1

Y1 - 1984/11/1

N2 - 3-Formyl-2-acetylenyl-1-methylindole oximes readily undergo intramolecular heterocyclization with closure of a pyridine ring and formation of substituted γ-carboline N-oxides.

AB - 3-Formyl-2-acetylenyl-1-methylindole oximes readily undergo intramolecular heterocyclization with closure of a pyridine ring and formation of substituted γ-carboline N-oxides.

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U2 - 10.1007/BF00948858

DO - 10.1007/BF00948858

M3 - Article

AN - SCOPUS:0037694382

VL - 33

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EP - 2385

JO - Russian Chemical Bulletin

JF - Russian Chemical Bulletin

SN - 0568-5230

IS - 11

ER -

Cyclizaticn of 3-formyl-2-acetylenylindole oximes

Abstract

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