A practical one-pot synthesis of 2,3-disubstituted indoles from unactivated anilines

Makoto Tokunaga; Mitsuru Ota; Masa aki Haga; Yasuo Wakatsuki

doi:10.1016/S0040-4039(01)00588-3

A practical one-pot synthesis of 2,3-disubstituted indoles from unactivated anilines

Makoto Tokunaga, Mitsuru Ota, Masa aki Haga, Yasuo Wakatsuki

研究成果: ジャーナルへの寄稿 › 学術誌 › 査読

53 被引用数 (Scopus)

抄録

2-Substituted-3-methyl indoles are synthesized with good regioselectivity from readily available substrates and catalysts, i.e. the reaction of anilines with propargyl alcohols in the presence of 0.36-1 mol% Ru₃(CO)₁₂.

本文言語	英語
ページ（範囲）	3865-3868
ページ数	4
ジャーナル	Tetrahedron Letters
巻	42
号	23
DOI	https://doi.org/10.1016/S0040-4039(01)00588-3
出版ステータス	出版済み - 6月 4 2001
外部発表	はい

!!!All Science Journal Classification (ASJC) codes

生化学
創薬
有機化学

文献へのアクセス

10.1016/S0040-4039(01)00588-3

他のファイルとリンク

引用スタイル

@article{0791df9bcdbe42c9899f8db9ca7b987b,

title = "A practical one-pot synthesis of 2,3-disubstituted indoles from unactivated anilines",

abstract = "2-Substituted-3-methyl indoles are synthesized with good regioselectivity from readily available substrates and catalysts, i.e. the reaction of anilines with propargyl alcohols in the presence of 0.36-1 mol% Ru3(CO)12.",

author = "Makoto Tokunaga and Mitsuru Ota and Haga, {Masa aki} and Yasuo Wakatsuki",

year = "2001",

month = jun,

day = "4",

doi = "10.1016/S0040-4039(01)00588-3",

language = "English",

volume = "42",

pages = "3865--3868",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Limited",

number = "23",

}

TY - JOUR

T1 - A practical one-pot synthesis of 2,3-disubstituted indoles from unactivated anilines

AU - Tokunaga, Makoto

AU - Ota, Mitsuru

AU - Haga, Masa aki

AU - Wakatsuki, Yasuo

PY - 2001/6/4

Y1 - 2001/6/4

N2 - 2-Substituted-3-methyl indoles are synthesized with good regioselectivity from readily available substrates and catalysts, i.e. the reaction of anilines with propargyl alcohols in the presence of 0.36-1 mol% Ru3(CO)12.

AB - 2-Substituted-3-methyl indoles are synthesized with good regioselectivity from readily available substrates and catalysts, i.e. the reaction of anilines with propargyl alcohols in the presence of 0.36-1 mol% Ru3(CO)12.

UR - http://www.scopus.com/inward/record.url?scp=0035806306&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0035806306&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(01)00588-3

DO - 10.1016/S0040-4039(01)00588-3

M3 - Article

AN - SCOPUS:0035806306

SN - 0040-4039

VL - 42

SP - 3865

EP - 3868

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 23

ER -

A practical one-pot synthesis of 2,3-disubstituted indoles from unactivated anilines

抄録

!!!All Science Journal Classification (ASJC) codes

文献へのアクセス

他のファイルとリンク

フィンガープリント

引用スタイル