An efficient route for the synthesis of benzimidazoles via a hydrogen-transfer strategy between o -nitroanilines and alcohols
Publication type: Journal Article
Publication date: 2016-10-01
scimago Q3
wos Q3
SJR: 0.334
CiteScore: 3.2
Impact factor: 1.5
ISSN: 00404039, 18733581
Organic Chemistry
Drug Discovery
Biochemistry
Abstract
[1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II) has been used as an efficient catalyst for the synthesis of 2-substituted benzimidazoles via a hydrogen-transfer strategy. Various 2-substituted benzimidazoles were synthesized in good to excellent yields (up to 97%). The reaction shows good functional group tolerance. And no additional additive, oxidant, or reductant was required for the reaction.
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27
Total citations:
27
Citations from 2024:
2
(7.41%)
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GOST
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Li Xiaotong X. et al. An efficient route for the synthesis of benzimidazoles via a hydrogen-transfer strategy between o -nitroanilines and alcohols // Tetrahedron Letters. 2016. Vol. 57. No. 41. pp. 4645-4649.
GOST all authors (up to 50)
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Li Xiaotong X., Hu R., Tong Y., Pan Q., Miao D., Han S. An efficient route for the synthesis of benzimidazoles via a hydrogen-transfer strategy between o -nitroanilines and alcohols // Tetrahedron Letters. 2016. Vol. 57. No. 41. pp. 4645-4649.
Cite this
RIS
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TY - JOUR
DO - 10.1016/j.tetlet.2016.09.018
UR - https://doi.org/10.1016/j.tetlet.2016.09.018
TI - An efficient route for the synthesis of benzimidazoles via a hydrogen-transfer strategy between o -nitroanilines and alcohols
T2 - Tetrahedron Letters
AU - Li Xiaotong, Xiaotong
AU - Hu, Renhe
AU - Tong, Yao
AU - Pan, Qiang
AU - Miao, Dazhuang
AU - Han, Shiqing
PY - 2016
DA - 2016/10/01
PB - Elsevier
SP - 4645-4649
IS - 41
VL - 57
SN - 0040-4039
SN - 1873-3581
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2016_Li Xiaotong,
author = {Xiaotong Li Xiaotong and Renhe Hu and Yao Tong and Qiang Pan and Dazhuang Miao and Shiqing Han},
title = {An efficient route for the synthesis of benzimidazoles via a hydrogen-transfer strategy between o -nitroanilines and alcohols},
journal = {Tetrahedron Letters},
year = {2016},
volume = {57},
publisher = {Elsevier},
month = {oct},
url = {https://doi.org/10.1016/j.tetlet.2016.09.018},
number = {41},
pages = {4645--4649},
doi = {10.1016/j.tetlet.2016.09.018}
}
Cite this
MLA
Copy
Li Xiaotong, Xiaotong, et al. “An efficient route for the synthesis of benzimidazoles via a hydrogen-transfer strategy between o -nitroanilines and alcohols.” Tetrahedron Letters, vol. 57, no. 41, Oct. 2016, pp. 4645-4649. https://doi.org/10.1016/j.tetlet.2016.09.018.