Alkynes as Privileged Synthons in Selected Organic Name Reactions.
Publication type: Journal Article
Publication date: 2019-03-03
scimago Q3
wos Q2
SJR: 0.377
CiteScore: 4.0
Impact factor: 2.5
ISSN: 15701794, 18756271
PubMed ID:
31975673
Organic Chemistry
Biochemistry
Abstract
BACKGROUND
Alkynes are actually basic chemicals, serving as privileged synthons for planning new organic reactions for assemblage of a reactive motif, which easily undergoes a further desirable transformation. Name reactions, in organic chemistry are referred to those reactions which are well-recognized and reached to such status for being called as their explorers, discoverers or developers. Alkynes have been used in various name reactions. In this review, we try to underscore the applications of alkynes as privileged synthons in prevalent name reactions such as Huisgen 1,3-dipolar cycloaddtion via Click reaction, Sonogashira reaction, and Hetero Diels-Alder reaction.
OBJECTIVE
In this review, we try to underscore the applications of alkynes as privileged synthons in the formation of heterocycles, focused on the selected reactions of alkynes as a synthon or impending utilization in synthetic organic chemistry, which have reached such high status for being included in the list of name reactions in organic chemistry.
CONCLUSION
Alkynes (including acetylene) are an unsaturated hydrocarbon bearing one or more triple C-C bond. Remarkably, alkynes and their derivatives are frequently being used as molecular scaffolds for planning new organic reactions and installing reactive functional group for further reaction. It is worth mentioning that in general, the terminal alkynes are more useful and more frequently being used in the art of organic synthesis. Remarkably, alkynes have found different applications in pharmacology, nanotechnology, as well as being known as appropriate starting precursors for the total synthesis of natural products and biologically active complex compounds. They are predominantly applied in various name reactions such as Sonogashira, Glaser reaction, Friedel-crafts reaction, Castro-Stephens coupling, Huisgen 1.3-dipolar cycloaddtion reaction via Click reaction, Sonogashira reaction, hetero-Diels-Alder reaction. In this review, we tried to impress the readers by presenting selected name reactions, which use the alkynes as either stating materials or precursors. We disclosed the applications of alkynes as a privileged synthons in several popular reactions, which reached to such high status being classified as name reactions. They are thriving and well known and established name reactions in organic chemistry such as Regioselective, 1,3-dipolar Huisgen cycloaddtion reaction via Click reaction, Sonogashira reaction and Diels-Alder reaction.
Found
Nothing found, try to update filter.
Found
Nothing found, try to update filter.
Top-30
Journals
|
1
2
3
|
|
|
Organic Letters
3 publications, 10%
|
|
|
Organic and Biomolecular Chemistry
3 publications, 10%
|
|
|
Russian Chemical Reviews
2 publications, 6.67%
|
|
|
Mendeleev Communications
2 publications, 6.67%
|
|
|
Journal of Organic Chemistry
2 publications, 6.67%
|
|
|
Chemical Communications
2 publications, 6.67%
|
|
|
Advances in Heterocyclic Chemistry
1 publication, 3.33%
|
|
|
Molecules
1 publication, 3.33%
|
|
|
Catalysis Letters
1 publication, 3.33%
|
|
|
Inorganica Chimica Acta
1 publication, 3.33%
|
|
|
Chemical Reviews
1 publication, 3.33%
|
|
|
Journal of Molecular Liquids
1 publication, 3.33%
|
|
|
Green Chemistry
1 publication, 3.33%
|
|
|
Physical Chemistry Chemical Physics
1 publication, 3.33%
|
|
|
Advanced Synthesis and Catalysis
1 publication, 3.33%
|
|
|
Process Safety and Environmental Protection
1 publication, 3.33%
|
|
|
Nature Chemistry
1 publication, 3.33%
|
|
|
Steroids
1 publication, 3.33%
|
|
|
ACS Catalysis
1 publication, 3.33%
|
|
|
Journal of Catalysis
1 publication, 3.33%
|
|
|
1
2
3
|
Publishers
|
1
2
3
4
5
6
7
|
|
|
Elsevier
7 publications, 23.33%
|
|
|
American Chemical Society (ACS)
7 publications, 23.33%
|
|
|
Royal Society of Chemistry (RSC)
7 publications, 23.33%
|
|
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
2 publications, 6.67%
|
|
|
Springer Nature
2 publications, 6.67%
|
|
|
OOO Zhurnal "Mendeleevskie Soobshcheniya"
2 publications, 6.67%
|
|
|
Wiley
2 publications, 6.67%
|
|
|
MDPI
1 publication, 3.33%
|
|
|
1
2
3
4
5
6
7
|
- We do not take into account publications without a DOI.
- Statistics recalculated weekly.
Are you a researcher?
Create a profile to get free access to personal recommendations for colleagues and new articles.
Metrics
30
Total citations:
30
Citations from 2024:
11
(36.67%)
Cite this
GOST |
RIS |
BibTex |
MLA
Cite this
GOST
Copy
HERAVI M. M. et al. Alkynes as Privileged Synthons in Selected Organic Name Reactions. // Current Organic Synthesis. 2019. Vol. 16. No. 2. pp. 205-243.
GOST all authors (up to 50)
Copy
HERAVI M. M., Dehghani M., Zadsirjan V., Ghanbarian M. Alkynes as Privileged Synthons in Selected Organic Name Reactions. // Current Organic Synthesis. 2019. Vol. 16. No. 2. pp. 205-243.
Cite this
RIS
Copy
TY - JOUR
DO - 10.2174/1570179416666190126100744
UR - https://doi.org/10.2174/1570179416666190126100744
TI - Alkynes as Privileged Synthons in Selected Organic Name Reactions.
T2 - Current Organic Synthesis
AU - HERAVI, MAJID M.
AU - Dehghani, Mahzad
AU - Zadsirjan, Vahideh
AU - Ghanbarian, Manijheh
PY - 2019
DA - 2019/03/03
PB - Bentham Science Publishers Ltd.
SP - 205-243
IS - 2
VL - 16
PMID - 31975673
SN - 1570-1794
SN - 1875-6271
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2019_HERAVI,
author = {MAJID M. HERAVI and Mahzad Dehghani and Vahideh Zadsirjan and Manijheh Ghanbarian},
title = {Alkynes as Privileged Synthons in Selected Organic Name Reactions.},
journal = {Current Organic Synthesis},
year = {2019},
volume = {16},
publisher = {Bentham Science Publishers Ltd.},
month = {mar},
url = {https://doi.org/10.2174/1570179416666190126100744},
number = {2},
pages = {205--243},
doi = {10.2174/1570179416666190126100744}
}
Cite this
MLA
Copy
HERAVI, MAJID M., et al. “Alkynes as Privileged Synthons in Selected Organic Name Reactions..” Current Organic Synthesis, vol. 16, no. 2, Mar. 2019, pp. 205-243. https://doi.org/10.2174/1570179416666190126100744.