Standard

A one-pot synthesis of 1-arylalka-1,3-diynes by sequential acetylene zipper and Sonogashira reactions. / Balova, Irina A.; Morozkina, Svetlana N.; Knight, David W.; Vasilevsky, Sergei F.

In: Tetrahedron Letters, Vol. 44, No. 1, 01.01.2003, p. 107-109.

Research output: Contribution to journalArticlepeer-review

Harvard

Balova, IA, Morozkina, SN, Knight, DW & Vasilevsky, SF 2003, 'A one-pot synthesis of 1-arylalka-1,3-diynes by sequential acetylene zipper and Sonogashira reactions', Tetrahedron Letters, vol. 44, no. 1, pp. 107-109. https://doi.org/10.1016/S0040-4039(02)02496-6

APA

Vancouver

Author

Balova, Irina A. ; Morozkina, Svetlana N. ; Knight, David W. ; Vasilevsky, Sergei F. / A one-pot synthesis of 1-arylalka-1,3-diynes by sequential acetylene zipper and Sonogashira reactions. In: Tetrahedron Letters. 2003 ; Vol. 44, No. 1. pp. 107-109.

BibTeX

@article{f98d9eb830e7423791e4a83d61324581,
title = "A one-pot synthesis of 1-arylalka-1,3-diynes by sequential acetylene zipper and Sonogashira reactions",
abstract = "1,3-Diynes, formed in situ by base-induced acetylene zipper reactions, following anion quenching with water, undergo smooth Sonogashira-type couplings with functionalized aryl iodides, to give good overall yields of 1-arylalka-1,3-diynes.",
author = "Balova, {Irina A.} and Morozkina, {Svetlana N.} and Knight, {David W.} and Vasilevsky, {Sergei F.}",
note = "Funding Information: We gratefully acknowledge financial support from INTAS, Grant 97-31999 and RFBR Grant 02-03-32229.",
year = "2003",
month = jan,
day = "1",
doi = "10.1016/S0040-4039(02)02496-6",
language = "English",
volume = "44",
pages = "107--109",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier",
number = "1",

}

RIS

TY - JOUR

T1 - A one-pot synthesis of 1-arylalka-1,3-diynes by sequential acetylene zipper and Sonogashira reactions

AU - Balova, Irina A.

AU - Morozkina, Svetlana N.

AU - Knight, David W.

AU - Vasilevsky, Sergei F.

N1 - Funding Information: We gratefully acknowledge financial support from INTAS, Grant 97-31999 and RFBR Grant 02-03-32229.

PY - 2003/1/1

Y1 - 2003/1/1

N2 - 1,3-Diynes, formed in situ by base-induced acetylene zipper reactions, following anion quenching with water, undergo smooth Sonogashira-type couplings with functionalized aryl iodides, to give good overall yields of 1-arylalka-1,3-diynes.

AB - 1,3-Diynes, formed in situ by base-induced acetylene zipper reactions, following anion quenching with water, undergo smooth Sonogashira-type couplings with functionalized aryl iodides, to give good overall yields of 1-arylalka-1,3-diynes.

UR - http://www.scopus.com/inward/record.url?scp=0037213004&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(02)02496-6

DO - 10.1016/S0040-4039(02)02496-6

M3 - Article

AN - SCOPUS:0037213004

VL - 44

SP - 107

EP - 109

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 1

ER -

ID: 96688029