Diversifying the superbase-catalyzed C=N bond ethynylation: triaryl-1-pyrrolines and triaryl-1H-pyrroles from N-benzyl aldimines and arylacetylenes
Publication type: Journal Article
Publication date: 2023-01-01
scimago Q3
wos Q3
SJR: 0.305
CiteScore: 3.0
Impact factor: 1.7
ISSN: 09599436, 1364551X
General Chemistry
Abstract
N-Benzyl aldimines react with arylacetylenes in the presence of ButOK/DMSO superbase system to afford 2,3,5-triaryl-1-pyrrolines as two tautomers with 1,2- and 1,5-location of the double bond, both being the trans-diastereomers. This version of the C=N bond ethynylation differs from the previous one with N-benzyl ketimines. The oxidation of the pyrroline tautomeric mixtures without their isolation gives 2,3,5-triaryl-1H-pyrroles.
Found
Nothing found, try to update filter.
Found
Nothing found, try to update filter.
Top-30
Journals
|
1
2
|
|
|
Mendeleev Communications
2 publications, 25%
|
|
|
Journal of Organic Chemistry
1 publication, 12.5%
|
|
|
Russian Journal of Organic Chemistry
1 publication, 12.5%
|
|
|
Organic Letters
1 publication, 12.5%
|
|
|
Журнал органической химии
1 publication, 12.5%
|
|
|
Russian Chemical Reviews
1 publication, 12.5%
|
|
|
ACS Omega
1 publication, 12.5%
|
|
|
1
2
|
Publishers
|
1
2
3
|
|
|
American Chemical Society (ACS)
3 publications, 37.5%
|
|
|
OOO Zhurnal "Mendeleevskie Soobshcheniya"
2 publications, 25%
|
|
|
Pleiades Publishing
1 publication, 12.5%
|
|
|
Akademizdatcenter Nauka
1 publication, 12.5%
|
|
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 12.5%
|
|
|
1
2
3
|
- 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
8
Total citations:
8
Citations from 2024:
5
(62.5%)
Cite this
GOST |
RIS |
BibTex |
MLA
Cite this
GOST
Copy
Bidusenko I. A. et al. Diversifying the superbase-catalyzed C=N bond ethynylation: triaryl-1-pyrrolines and triaryl-1H-pyrroles from N-benzyl aldimines and arylacetylenes // Mendeleev Communications. 2023. Vol. 33. No. 1. pp. 24-26.
GOST all authors (up to 50)
Copy
Bidusenko I. A., Schmidt E. Yu., Protsuk N. I., Ushakov I. A., Trofimov B. A. Diversifying the superbase-catalyzed C=N bond ethynylation: triaryl-1-pyrrolines and triaryl-1H-pyrroles from N-benzyl aldimines and arylacetylenes // Mendeleev Communications. 2023. Vol. 33. No. 1. pp. 24-26.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1016/j.mencom.2023.01.007
UR - https://doi.org/10.1016/j.mencom.2023.01.007
TI - Diversifying the superbase-catalyzed C=N bond ethynylation: triaryl-1-pyrrolines and triaryl-1H-pyrroles from N-benzyl aldimines and arylacetylenes
T2 - Mendeleev Communications
AU - Bidusenko, Ivan A
AU - Schmidt, Elena Yu
AU - Protsuk, Nadezhda I
AU - Ushakov, I A
AU - Trofimov, B. A.
PY - 2023
DA - 2023/01/01
PB - OOO Zhurnal "Mendeleevskie Soobshcheniya"
SP - 24-26
IS - 1
VL - 33
SN - 0959-9436
SN - 1364-551X
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2023_Bidusenko,
author = {Ivan A Bidusenko and Elena Yu Schmidt and Nadezhda I Protsuk and I A Ushakov and B. A. Trofimov},
title = {Diversifying the superbase-catalyzed C=N bond ethynylation: triaryl-1-pyrrolines and triaryl-1H-pyrroles from N-benzyl aldimines and arylacetylenes},
journal = {Mendeleev Communications},
year = {2023},
volume = {33},
publisher = {OOO Zhurnal "Mendeleevskie Soobshcheniya"},
month = {jan},
url = {https://doi.org/10.1016/j.mencom.2023.01.007},
number = {1},
pages = {24--26},
doi = {10.1016/j.mencom.2023.01.007}
}
Cite this
MLA
Copy
Bidusenko, Ivan A., et al. “Diversifying the superbase-catalyzed C=N bond ethynylation: triaryl-1-pyrrolines and triaryl-1H-pyrroles from N-benzyl aldimines and arylacetylenes.” Mendeleev Communications, vol. 33, no. 1, Jan. 2023, pp. 24-26. https://doi.org/10.1016/j.mencom.2023.01.007.
Profiles