volume 52 issue 12 pages 1002-1004

Synthesis of 1,3-dihydro-2H-benzimidazol-2-ones (microreview)

Publication typeJournal Article
Publication date2016-12-01
scimago Q4
wos Q4
SJR0.243
CiteScore2.7
Impact factor1.0
ISSN00093122, 15738353
Organic Chemistry
Abstract
This microreview covers data regarding the synthesis of 1,3-dihydro-2H-benzimidazol-2-ones published during the last five years. The synthetic routes to benzimidazolones can be classified into several types: cyclocarbonylation of 1,2-diaminobenzenes, transformation of benzimidazolium salts, synthesis from arylureas, a Curtius reaction of anthranilic acids or phthalic anhydrides, and other pathways.
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Armenta R., Sarmiento Sánchez J. I. Synthesis of 1,3-dihydro-2H-benzimidazol-2-ones (microreview) // Chemistry of Heterocyclic Compounds. 2016. Vol. 52. No. 12. pp. 1002-1004.
GOST all authors (up to 50) Copy
Armenta R., Sarmiento Sánchez J. I. Synthesis of 1,3-dihydro-2H-benzimidazol-2-ones (microreview) // Chemistry of Heterocyclic Compounds. 2016. Vol. 52. No. 12. pp. 1002-1004.
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RIS Copy
TY - JOUR
DO - 10.1007/s10593-017-1999-7
UR - https://doi.org/10.1007/s10593-017-1999-7
TI - Synthesis of 1,3-dihydro-2H-benzimidazol-2-ones (microreview)
T2 - Chemistry of Heterocyclic Compounds
AU - Armenta, Ramón
AU - Sarmiento Sánchez, Juan I
PY - 2016
DA - 2016/12/01
PB - Springer Nature
SP - 1002-1004
IS - 12
VL - 52
SN - 0009-3122
SN - 1573-8353
ER -
BibTex |
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BibTex (up to 50 authors) Copy
@article{2016_Armenta,
author = {Ramón Armenta and Juan I Sarmiento Sánchez},
title = {Synthesis of 1,3-dihydro-2H-benzimidazol-2-ones (microreview)},
journal = {Chemistry of Heterocyclic Compounds},
year = {2016},
volume = {52},
publisher = {Springer Nature},
month = {dec},
url = {https://doi.org/10.1007/s10593-017-1999-7},
number = {12},
pages = {1002--1004},
doi = {10.1007/s10593-017-1999-7}
}
MLA
Cite this
MLA Copy
Armenta, Ramón, and Juan I Sarmiento Sánchez. “Synthesis of 1,3-dihydro-2H-benzimidazol-2-ones (microreview).” Chemistry of Heterocyclic Compounds, vol. 52, no. 12, Dec. 2016, pp. 1002-1004. https://doi.org/10.1007/s10593-017-1999-7.