RhCl3/amine-catalyzed cyclotrimerization of alkynes

Kenta Yoshida; Ichiro Morimoto; Koichi Mitsudo; Hideo Tanaka

doi:10.1246/cl.2007.998

RhCl₃/amine-catalyzed cyclotrimerization of alkynes

Kenta Yoshida, Ichiro Morimoto, Koichi Mitsudo, Hideo Tanaka

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

23 Citations (Scopus)

Abstract

RhCl₃/amine was found to be an efficient catalyst for the cyclotrimerization of alkynes. The [2 + 2 + 2] cyclotrimerization of internal alkynes proceeded smoothly to afford hexa-substituted benzenes regioselectively in moderate to high yields.

Original language	English
Pages (from-to)	998-999
Number of pages	2
Journal	Chemistry Letters
Volume	36
Issue number	8
DOIs	https://doi.org/10.1246/cl.2007.998
Publication status	Published - Aug 5 2007

ASJC Scopus subject areas

Chemistry(all)

Access to Document

10.1246/cl.2007.998

Fingerprint Dive into the research topics of 'RhCl<sub>3</sub>/amine-catalyzed cyclotrimerization of alkynes'. Together they form a unique fingerprint.

Cite this

@article{609f1d6195184038b2e37aef48487b83,

title = "RhCl3/amine-catalyzed cyclotrimerization of alkynes",

abstract = "RhCl3/amine was found to be an efficient catalyst for the cyclotrimerization of alkynes. The [2 + 2 + 2] cyclotrimerization of internal alkynes proceeded smoothly to afford hexa-substituted benzenes regioselectively in moderate to high yields.",

author = "Kenta Yoshida and Ichiro Morimoto and Koichi Mitsudo and Hideo Tanaka",

year = "2007",

month = aug,

day = "5",

doi = "10.1246/cl.2007.998",

language = "English",

volume = "36",

pages = "998--999",

journal = "Chemistry Letters",

issn = "0366-7022",

publisher = "Chemical Society of Japan",

number = "8",

}

TY - JOUR

T1 - RhCl3/amine-catalyzed cyclotrimerization of alkynes

AU - Yoshida, Kenta

AU - Morimoto, Ichiro

AU - Mitsudo, Koichi

AU - Tanaka, Hideo

PY - 2007/8/5

Y1 - 2007/8/5

N2 - RhCl3/amine was found to be an efficient catalyst for the cyclotrimerization of alkynes. The [2 + 2 + 2] cyclotrimerization of internal alkynes proceeded smoothly to afford hexa-substituted benzenes regioselectively in moderate to high yields.

AB - RhCl3/amine was found to be an efficient catalyst for the cyclotrimerization of alkynes. The [2 + 2 + 2] cyclotrimerization of internal alkynes proceeded smoothly to afford hexa-substituted benzenes regioselectively in moderate to high yields.

UR - http://www.scopus.com/inward/record.url?scp=34548321129&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=34548321129&partnerID=8YFLogxK

U2 - 10.1246/cl.2007.998

DO - 10.1246/cl.2007.998

M3 - Article

AN - SCOPUS:34548321129

VL - 36

SP - 998

EP - 999

JO - Chemistry Letters

JF - Chemistry Letters

SN - 0366-7022

IS - 8

ER -