Silver(I)-Catalyzed Enantioselective [3+2]-Cycloaddition Reaction of α-Silylimines: A Facile Route to Quaternary-Carbon-Rich Scaffolds
Publication type: Journal Article
Publication date: 2016-11-08
scimago Q1
wos Q2
SJR: 0.981
CiteScore: 6.7
Impact factor: 3.7
ISSN: 09476539, 15213765
PubMed ID:
27740700
General Chemistry
Catalysis
Organic Chemistry
Abstract
A silver-catalyzed highly enantioselective 1,3-dipolar cycloaddition reaction of α-silylimines with pyrone-based trisubstituted olefins was developed affording bi- and tricyclic α-quaternary-carbon-rich pyrano-pyrrolidines in excellent yields. The tricyclic benzopyrone adducts thus obtained were efficiently transformed into highly complex tetracyclic scaffolds supporting four consecutive stereogenic centers with three quaternary carbons.
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19
Total citations:
19
Citations from 2024:
3
(16.67%)
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GOST
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Kesava Reddy N. et al. Silver(I)-Catalyzed Enantioselective [3+2]-Cycloaddition Reaction of α-Silylimines: A Facile Route to Quaternary-Carbon-Rich Scaffolds // Chemistry - A European Journal. 2016. Vol. 22. No. 51. pp. 18373-18377.
GOST all authors (up to 50)
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Kesava Reddy N., Golz C., Strohmann C., Kumar K. Silver(I)-Catalyzed Enantioselective [3+2]-Cycloaddition Reaction of α-Silylimines: A Facile Route to Quaternary-Carbon-Rich Scaffolds // Chemistry - A European Journal. 2016. Vol. 22. No. 51. pp. 18373-18377.
Cite this
RIS
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TY - JOUR
DO - 10.1002/chem.201604793
UR - https://doi.org/10.1002/chem.201604793
TI - Silver(I)-Catalyzed Enantioselective [3+2]-Cycloaddition Reaction of α-Silylimines: A Facile Route to Quaternary-Carbon-Rich Scaffolds
T2 - Chemistry - A European Journal
AU - Kesava Reddy, Naredla
AU - Golz, Christopher
AU - Strohmann, Carsten
AU - Kumar, Kamal
PY - 2016
DA - 2016/11/08
PB - Wiley
SP - 18373-18377
IS - 51
VL - 22
PMID - 27740700
SN - 0947-6539
SN - 1521-3765
ER -
Cite this
BibTex (up to 50 authors)
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@article{2016_Kesava Reddy,
author = {Naredla Kesava Reddy and Christopher Golz and Carsten Strohmann and Kamal Kumar},
title = {Silver(I)-Catalyzed Enantioselective [3+2]-Cycloaddition Reaction of α-Silylimines: A Facile Route to Quaternary-Carbon-Rich Scaffolds},
journal = {Chemistry - A European Journal},
year = {2016},
volume = {22},
publisher = {Wiley},
month = {nov},
url = {https://doi.org/10.1002/chem.201604793},
number = {51},
pages = {18373--18377},
doi = {10.1002/chem.201604793}
}
Cite this
MLA
Copy
Kesava Reddy, Naredla, et al. “Silver(I)-Catalyzed Enantioselective [3+2]-Cycloaddition Reaction of α-Silylimines: A Facile Route to Quaternary-Carbon-Rich Scaffolds.” Chemistry - A European Journal, vol. 22, no. 51, Nov. 2016, pp. 18373-18377. https://doi.org/10.1002/chem.201604793.