volume 26 issue 27

Synthesis of Heterocycles from 2‐Acylbenzoic Acids

Publication typeJournal Article
Publication date2023-06-20
scimago Q2
wos Q2
SJR0.558
CiteScore4.3
Impact factor2.7
ISSN1434193X, 10990690
Organic Chemistry
Physical and Theoretical Chemistry
Abstract

Heterocyclics are the crucial scaffolds present in pharmaceuticals, natural products, biologically active compounds and agrochemicals. Consequently, the development of simple and practical methods for constructing heterocyclics has always been a fascinating field in organic synthesis. Recently, 2‐acylbenzoic acids, highly reactive and versatile synthons, have been broadly applied in the construction of heterocycles due to their multiple reaction sites. In this review, we summarized recent progress in the application of 2‐acylbenzoic acids for the synthesis of heterocycles including phthalides, isochromanones, isoindolines, phthalazinones, and quinolones. The substrate scopes, proposed mechanisms, and product application of different types of reactions are discussed.

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GOST Copy
Liu Y., Li C., Yang G. P. Synthesis of Heterocycles from 2‐Acylbenzoic Acids // European Journal of Organic Chemistry. 2023. Vol. 26. No. 27.
GOST all authors (up to 50) Copy
Liu Y., Li C., Yang G. P. Synthesis of Heterocycles from 2‐Acylbenzoic Acids // European Journal of Organic Chemistry. 2023. Vol. 26. No. 27.
RIS |
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RIS Copy
TY - JOUR
DO - 10.1002/ejoc.202300452
UR - https://doi.org/10.1002/ejoc.202300452
TI - Synthesis of Heterocycles from 2‐Acylbenzoic Acids
T2 - European Journal of Organic Chemistry
AU - Liu, Yu-Feng
AU - Li, Cui
AU - Yang, Guo Ping
PY - 2023
DA - 2023/06/20
PB - Wiley
IS - 27
VL - 26
SN - 1434-193X
SN - 1099-0690
ER -
BibTex
Cite this
BibTex (up to 50 authors) Copy
@article{2023_Liu,
author = {Yu-Feng Liu and Cui Li and Guo Ping Yang},
title = {Synthesis of Heterocycles from 2‐Acylbenzoic Acids},
journal = {European Journal of Organic Chemistry},
year = {2023},
volume = {26},
publisher = {Wiley},
month = {jun},
url = {https://doi.org/10.1002/ejoc.202300452},
number = {27},
doi = {10.1002/ejoc.202300452}
}