Green Chemistry

, том 24 , издание 2 , страницы 748-753

Methanol as the C₁ source: redox coupling of nitrobenzenes and alcohols for the synthesis of benzimidazoles

Тип публикации: Journal Article

Дата публикации: 2022-01-01

Royal Society of Chemistry (RSC)

Green Chemistry

SCImago Q1

Tоп 10% SCImago

WOS Q1

БС1

SJR: 1.811

CiteScore: 16

Impact factor: 10.6

ISSN: 14639262, 14639270

DOI: 10.1039/d1gc03907e

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Environmental Chemistry

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Краткое описание

We present an operationally simple redox coupling for the synthesis of N-1 substituted benzimidazoles using feedstock building block 2-nitroaniline derivatives as the precursors and methanol as the C1 source. Higher atom, step, and redox economies and excellent regioselectivity were achieved compared with conventional synthesis using diaminobenzene and formic acid derivatives.

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Journal of Organic Chemistry	Journal of Organic Chemistry, 3, 13.64% Journal of Organic Chemistry 3 публикации, 13.64%
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Organic and Biomolecular Chemistry	Organic and Biomolecular Chemistry, 2, 9.09% Organic and Biomolecular Chemistry 2 публикации, 9.09%
Coordination Chemistry Reviews	Coordination Chemistry Reviews, 2, 9.09% Coordination Chemistry Reviews 2 публикации, 9.09%
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Applied Catalysis B: Environmental	Applied Catalysis B: Environmental, 1, 4.55% Applied Catalysis B: Environmental 1 публикация, 4.55%
Synthetic Communications	Synthetic Communications, 1, 4.55% Synthetic Communications 1 публикация, 4.55%
Asian Journal of Organic Chemistry	Asian Journal of Organic Chemistry, 1, 4.55% Asian Journal of Organic Chemistry 1 публикация, 4.55%
Molecular Catalysis	Molecular Catalysis, 1, 4.55% Molecular Catalysis 1 публикация, 4.55%
Advanced Synthesis and Catalysis	Advanced Synthesis and Catalysis, 1, 4.55% Advanced Synthesis and Catalysis 1 публикация, 4.55%
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American Chemical Society (ACS)	American Chemical Society (ACS), 7, 31.82% American Chemical Society (ACS) 7 публикаций, 31.82%
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ГОСТ |

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Li H. et al. Methanol as the C1 source: redox coupling of nitrobenzenes and alcohols for the synthesis of benzimidazoles // Green Chemistry. 2022. Vol. 24. No. 2. pp. 748-753.

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Li H., Zhang Y., Yan Z., Lai Z., Yang R., Peng M., Sun Y., AN J. Methanol as the C1 source: redox coupling of nitrobenzenes and alcohols for the synthesis of benzimidazoles // Green Chemistry. 2022. Vol. 24. No. 2. pp. 748-753.

RIS |

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TY - JOUR

DO - 10.1039/d1gc03907e

UR - https://xlink.rsc.org/?DOI=D1GC03907E

TI - Methanol as the C1 source: redox coupling of nitrobenzenes and alcohols for the synthesis of benzimidazoles

T2 - Green Chemistry

AU - Li, Hengzhao

AU - Zhang, Yuntong

AU - Yan, Zihan

AU - Lai, Zemin

AU - Yang, Ruoyan

AU - Peng, Mengqi

AU - Sun, Yanhao

AU - AN, JIE

PY - 2022

DA - 2022/01/01

PB - Royal Society of Chemistry (RSC)

SP - 748-753

IS - 2

VL - 24

SN - 1463-9262

SN - 1463-9270

ER -

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@article{2022_Li,

author = {Hengzhao Li and Yuntong Zhang and Zihan Yan and Zemin Lai and Ruoyan Yang and Mengqi Peng and Yanhao Sun and JIE AN},

title = {Methanol as the C1 source: redox coupling of nitrobenzenes and alcohols for the synthesis of benzimidazoles},

journal = {Green Chemistry},

year = {2022},

volume = {24},

publisher = {Royal Society of Chemistry (RSC)},

month = {jan},

url = {https://xlink.rsc.org/?DOI=D1GC03907E},

number = {2},

pages = {748--753},

doi = {10.1039/d1gc03907e}

}

MLA

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MLA Скопировать

Li, Hengzhao, et al. “Methanol as the C1 source: redox coupling of nitrobenzenes and alcohols for the synthesis of benzimidazoles.” Green Chemistry, vol. 24, no. 2, Jan. 2022, pp. 748-753. https://xlink.rsc.org/?DOI=D1GC03907E.

Издатель

Royal Society of Chemistry (RSC)

Журнал

Green Chemistry

SCImago Q1

Tоп 10% SCImago

WOS Q1

БС1

SJR

1.811

CiteScore

Impact factor