volume 119 pages 154413

Difluorocarbene enabled ester insertion/1,4-acyl rearrangement of 2-acetoxylpyridines: Modular access to gem-difluoromethylenated 2-pyridones

Publication typeJournal Article
Publication date2023-04-01
scimago Q3
wos Q3
SJR0.334
CiteScore3.2
Impact factor1.5
ISSN00404039, 18733581
Organic Chemistry
Drug Discovery
Biochemistry
Abstract
An efficient and simple protocol for the construction of gem-difluoromethylenated 2-pyridones via difluorocarbene enabled ester insertion/acyl rearrangement of 2-acetoxylpyridines and (bromodifluoromethyl)trimethylsilane has been documented. The reactions feature transition-metal free, mild reaction conditions and excellent functional group compatibility. The late-stage modification of bioactive molecules, scaled-up reaction, and synthetic transformations demonstrated the practicability of this protocol.
Found 
Found 

Top-30

Journals

1
2
Journal of Organic Chemistry
2 publications, 33.33%
European Journal of Organic Chemistry
1 publication, 16.67%
Organic and Biomolecular Chemistry
1 publication, 16.67%
Chemical Record
1 publication, 16.67%
Journal of Inorganic and Organometallic Polymers and Materials
1 publication, 16.67%
1
2

Publishers

1
2
Wiley
2 publications, 33.33%
American Chemical Society (ACS)
2 publications, 33.33%
Royal Society of Chemistry (RSC)
1 publication, 16.67%
Springer Nature
1 publication, 16.67%
1
2
  • 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
6
Share
Cite this
GOST |
Cite this
GOST Copy
Li S., Wang G., Ye Z. S. Difluorocarbene enabled ester insertion/1,4-acyl rearrangement of 2-acetoxylpyridines: Modular access to gem-difluoromethylenated 2-pyridones // Tetrahedron Letters. 2023. Vol. 119. p. 154413.
GOST all authors (up to 50) Copy
Li S., Wang G., Ye Z. S. Difluorocarbene enabled ester insertion/1,4-acyl rearrangement of 2-acetoxylpyridines: Modular access to gem-difluoromethylenated 2-pyridones // Tetrahedron Letters. 2023. Vol. 119. p. 154413.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.1016/j.tetlet.2023.154413
UR - https://doi.org/10.1016/j.tetlet.2023.154413
TI - Difluorocarbene enabled ester insertion/1,4-acyl rearrangement of 2-acetoxylpyridines: Modular access to gem-difluoromethylenated 2-pyridones
T2 - Tetrahedron Letters
AU - Li, Shiwei
AU - Wang, Gang
AU - Ye, Zhi Shi
PY - 2023
DA - 2023/04/01
PB - Elsevier
SP - 154413
VL - 119
SN - 0040-4039
SN - 1873-3581
ER -
BibTex
Cite this
BibTex (up to 50 authors) Copy
@article{2023_Li,
author = {Shiwei Li and Gang Wang and Zhi Shi Ye},
title = {Difluorocarbene enabled ester insertion/1,4-acyl rearrangement of 2-acetoxylpyridines: Modular access to gem-difluoromethylenated 2-pyridones},
journal = {Tetrahedron Letters},
year = {2023},
volume = {119},
publisher = {Elsevier},
month = {apr},
url = {https://doi.org/10.1016/j.tetlet.2023.154413},
pages = {154413},
doi = {10.1016/j.tetlet.2023.154413}
}