Cu-catalyzed transannulation reaction of pyridotriazoles with terminal alkynes under aerobic conditions: Efficient synthesis of indolizines

V. Helan; A. V. Gulevich; V. Gevorgyan

doi:10.1039/c4sc03358b

Cu-catalyzed transannulation reaction of pyridotriazoles with terminal alkynes under aerobic conditions: Efficient synthesis of indolizines

V. Helan, A. V. Gulevich, V. Gevorgyan

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

132 Scopus citations

Abstract

A Cu(i)-catalyzed denitrogenative transannulation reaction of pyridotriazoles with terminal alkynes en route to indolizines was developed. Compared to the previously reported Rh-catalyzed transannulation reaction, this Cu-catalyzed method features aerobic conditions and a much broader scope of pyridotriazoles and alkynes.

Original language	English (US)
Pages (from-to)	1928-1931
Number of pages	4
Journal	Chemical Science
Volume	6
Issue number	3
DOIs	https://doi.org/10.1039/c4sc03358b
State	Published - Mar 1 2015
Externally published	Yes

ASJC Scopus subject areas

Chemistry(all)

Access to Document

10.1039/c4sc03358b

Cite this

@article{d30b6a3a2bcd4f989bcc504e17c23e21,

title = "Cu-catalyzed transannulation reaction of pyridotriazoles with terminal alkynes under aerobic conditions: Efficient synthesis of indolizines",

abstract = "A Cu(i)-catalyzed denitrogenative transannulation reaction of pyridotriazoles with terminal alkynes en route to indolizines was developed. Compared to the previously reported Rh-catalyzed transannulation reaction, this Cu-catalyzed method features aerobic conditions and a much broader scope of pyridotriazoles and alkynes.",

author = "V. Helan and Gulevich, {A. V.} and V. Gevorgyan",

note = "Publisher Copyright: {\textcopyright} The Royal Society of Chemistry 2015.",

year = "2015",

month = mar,

day = "1",

doi = "10.1039/c4sc03358b",

language = "English (US)",

volume = "6",

pages = "1928--1931",

journal = "Chemical Science",

issn = "2041-6520",

publisher = "Royal Society of Chemistry",

number = "3",

}

TY - JOUR

T1 - Cu-catalyzed transannulation reaction of pyridotriazoles with terminal alkynes under aerobic conditions

T2 - Efficient synthesis of indolizines

AU - Helan, V.

AU - Gulevich, A. V.

AU - Gevorgyan, V.

N1 - Publisher Copyright: © The Royal Society of Chemistry 2015.

PY - 2015/3/1

Y1 - 2015/3/1

N2 - A Cu(i)-catalyzed denitrogenative transannulation reaction of pyridotriazoles with terminal alkynes en route to indolizines was developed. Compared to the previously reported Rh-catalyzed transannulation reaction, this Cu-catalyzed method features aerobic conditions and a much broader scope of pyridotriazoles and alkynes.

AB - A Cu(i)-catalyzed denitrogenative transannulation reaction of pyridotriazoles with terminal alkynes en route to indolizines was developed. Compared to the previously reported Rh-catalyzed transannulation reaction, this Cu-catalyzed method features aerobic conditions and a much broader scope of pyridotriazoles and alkynes.

UR - http://www.scopus.com/inward/record.url?scp=84923207216&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84923207216&partnerID=8YFLogxK

U2 - 10.1039/c4sc03358b

DO - 10.1039/c4sc03358b

M3 - Article

AN - SCOPUS:84923207216

SN - 2041-6520

VL - 6

SP - 1928

EP - 1931

JO - Chemical Science

JF - Chemical Science

IS - 3

ER -

Cu-catalyzed transannulation reaction of pyridotriazoles with terminal alkynes under aerobic conditions: Efficient synthesis of indolizines

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this