Ethynylation of Isoquinoline and Quinoline Derivatives with Calcium Carbide
Publication type: Journal Article
Publication date: 2017-07-14
scimago Q3
wos Q3
SJR: 0.437
CiteScore: 3.3
Impact factor: 1.4
ISSN: 09365214, 14372096
Organic Chemistry
Abstract
An operatically simple method for the ethynylation of isoquinolines and quinolines is described. The ionic adduct derived from an alkynoic ester and the N-heterocycle was attacked by calcium carbide to give the ethynylation product. The procedure uses tetrabutylammonium fluoride trihydrate as a catalyst in aqueous N,N-dimethylacetamide. Steric and electronic effects of various substituents on the outcome of the reaction were examined.
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GOST
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Samzadeh Kermani A. Ethynylation of Isoquinoline and Quinoline Derivatives with Calcium Carbide // Synlett. 2017. Vol. 28. No. 16. pp. 2126-2130.
GOST all authors (up to 50)
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Samzadeh Kermani A. Ethynylation of Isoquinoline and Quinoline Derivatives with Calcium Carbide // Synlett. 2017. Vol. 28. No. 16. pp. 2126-2130.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1055/s-0036-1590815
UR - https://doi.org/10.1055/s-0036-1590815
TI - Ethynylation of Isoquinoline and Quinoline Derivatives with Calcium Carbide
T2 - Synlett
AU - Samzadeh Kermani, A
PY - 2017
DA - 2017/07/14
PB - Georg Thieme Verlag KG
SP - 2126-2130
IS - 16
VL - 28
SN - 0936-5214
SN - 1437-2096
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2017_Samzadeh Kermani,
author = {A Samzadeh Kermani},
title = {Ethynylation of Isoquinoline and Quinoline Derivatives with Calcium Carbide},
journal = {Synlett},
year = {2017},
volume = {28},
publisher = {Georg Thieme Verlag KG},
month = {jul},
url = {https://doi.org/10.1055/s-0036-1590815},
number = {16},
pages = {2126--2130},
doi = {10.1055/s-0036-1590815}
}
Cite this
MLA
Copy
Samzadeh Kermani, A.. “Ethynylation of Isoquinoline and Quinoline Derivatives with Calcium Carbide.” Synlett, vol. 28, no. 16, Jul. 2017, pp. 2126-2130. https://doi.org/10.1055/s-0036-1590815.