Consecutive isomerization and cyclization of 3-(2-Aminophenyl)-1-arylprop- 2-yn-1-ols leading to 2-arylquinolines in the presence of potassium hydroxide

Chan Sik Cho; Na Young Lee; Tae Jeong Kim; Sang Chul Shim

doi:10.1002/jhet.5570410317

Consecutive isomerization and cyclization of 3-(2-Aminophenyl)-1-arylprop- 2-yn-1-ols leading to 2-arylquinolines in the presence of potassium hydroxide

Chan Sik Cho, Na Young Lee, Tae Jeong Kim, Sang Chul Shim

Department of Applied Chemistry

Kyungpook National University

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

16 Scopus citations

Abstract

3-(2-Aminophenyl)-1-arylprop-2-yn-1-ols are readily converted to 2-arylquinolines in good yields in ethanol at 80° in the presence of potassium hydroxide via domino isomerization and cyclization.

Original language	English
Pages (from-to)	409-411
Number of pages	3
Journal	Journal of Heterocyclic Chemistry
Volume	41
Issue number	3
DOIs	https://doi.org/10.1002/jhet.5570410317
State	Published - 2004

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title = "Consecutive isomerization and cyclization of 3-(2-Aminophenyl)-1-arylprop- 2-yn-1-ols leading to 2-arylquinolines in the presence of potassium hydroxide",

abstract = "3-(2-Aminophenyl)-1-arylprop-2-yn-1-ols are readily converted to 2-arylquinolines in good yields in ethanol at 80° in the presence of potassium hydroxide via domino isomerization and cyclization.",

author = "Cho, {Chan Sik} and Lee, {Na Young} and Kim, {Tae Jeong} and Shim, {Sang Chul}",

year = "2004",

doi = "10.1002/jhet.5570410317",

language = "English",

volume = "41",

pages = "409--411",

journal = "Journal of Heterocyclic Chemistry",

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publisher = "Wiley-Blackwell",

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T1 - Consecutive isomerization and cyclization of 3-(2-Aminophenyl)-1-arylprop- 2-yn-1-ols leading to 2-arylquinolines in the presence of potassium hydroxide

AU - Cho, Chan Sik

AU - Lee, Na Young

AU - Kim, Tae Jeong

AU - Shim, Sang Chul

PY - 2004

Y1 - 2004

N2 - 3-(2-Aminophenyl)-1-arylprop-2-yn-1-ols are readily converted to 2-arylquinolines in good yields in ethanol at 80° in the presence of potassium hydroxide via domino isomerization and cyclization.

AB - 3-(2-Aminophenyl)-1-arylprop-2-yn-1-ols are readily converted to 2-arylquinolines in good yields in ethanol at 80° in the presence of potassium hydroxide via domino isomerization and cyclization.

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U2 - 10.1002/jhet.5570410317

DO - 10.1002/jhet.5570410317

M3 - Article

AN - SCOPUS:3042765986

SN - 0022-152X

VL - 41

SP - 409

EP - 411

JO - Journal of Heterocyclic Chemistry

JF - Journal of Heterocyclic Chemistry

IS - 3

ER -

Consecutive isomerization and cyclization of 3-(2-Aminophenyl)-1-arylprop- 2-yn-1-ols leading to 2-arylquinolines in the presence of potassium hydroxide

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