Electrophilic addition of phenols to 1-vinyl-4,5,6,7-tetrahydroindole

M. V. Markova; A. I. Mikhaleva; M. V. Sigalov; L. V. Morozova; I. A. Aliev; B. A. Trofimov

doi:10.1007/BF00482492

Electrophilic addition of phenols to 1-vinyl-4,5,6,7-tetrahydroindole

M. V. Markova, A. I. Mikhaleva, M. V. Sigalov, L. V. Morozova, I. A. Aliev, B. A. Trofimov

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

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Abstract

Both uncatalyzed and acid-catalyzed (CH₃COOH) addition of phenols to 1-vinyl-4,5,6,7-tetrahydroindole gave 1-(1-aroxyethyl)-4,5,6,7-tetrahydroindoles. With increasing acidity of the phenol and in the presence of CF₃COOH the yield of adducts was lowered because of the oligomerization of 1-vinyl-4,5,6,7-tetrahydroindole.

Original language	English
Pages (from-to)	501-503
Number of pages	3
Journal	Chemistry of Heterocyclic Compounds
Volume	25
Issue number	5
DOIs	https://doi.org/10.1007/BF00482492
State	Published - 1 May 1989
Externally published	Yes

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Organic Chemistry

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title = "Electrophilic addition of phenols to 1-vinyl-4,5,6,7-tetrahydroindole",

abstract = "Both uncatalyzed and acid-catalyzed (CH3COOH) addition of phenols to 1-vinyl-4,5,6,7-tetrahydroindole gave 1-(1-aroxyethyl)-4,5,6,7-tetrahydroindoles. With increasing acidity of the phenol and in the presence of CF3COOH the yield of adducts was lowered because of the oligomerization of 1-vinyl-4,5,6,7-tetrahydroindole.",

author = "Markova, {M. V.} and Mikhaleva, {A. I.} and Sigalov, {M. V.} and Morozova, {L. V.} and Aliev, {I. A.} and Trofimov, {B. A.}",

year = "1989",

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doi = "10.1007/BF00482492",

language = "English",

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pages = "501--503",

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TY - JOUR

T1 - Electrophilic addition of phenols to 1-vinyl-4,5,6,7-tetrahydroindole

AU - Markova, M. V.

AU - Mikhaleva, A. I.

AU - Sigalov, M. V.

AU - Morozova, L. V.

AU - Aliev, I. A.

AU - Trofimov, B. A.

PY - 1989/5/1

Y1 - 1989/5/1

N2 - Both uncatalyzed and acid-catalyzed (CH3COOH) addition of phenols to 1-vinyl-4,5,6,7-tetrahydroindole gave 1-(1-aroxyethyl)-4,5,6,7-tetrahydroindoles. With increasing acidity of the phenol and in the presence of CF3COOH the yield of adducts was lowered because of the oligomerization of 1-vinyl-4,5,6,7-tetrahydroindole.

AB - Both uncatalyzed and acid-catalyzed (CH3COOH) addition of phenols to 1-vinyl-4,5,6,7-tetrahydroindole gave 1-(1-aroxyethyl)-4,5,6,7-tetrahydroindoles. With increasing acidity of the phenol and in the presence of CF3COOH the yield of adducts was lowered because of the oligomerization of 1-vinyl-4,5,6,7-tetrahydroindole.

UR - http://www.scopus.com/inward/record.url?scp=34249973349&partnerID=8YFLogxK

U2 - 10.1007/BF00482492

DO - 10.1007/BF00482492

M3 - Article

AN - SCOPUS:34249973349

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VL - 25

SP - 501

EP - 503

JO - Chemistry of Heterocyclic Compounds

JF - Chemistry of Heterocyclic Compounds

IS - 5

ER -

Electrophilic addition of phenols to 1-vinyl-4,5,6,7-tetrahydroindole

Abstract

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