Organic Letters

, том 17 , издание 10 , страницы 2562-2565

Concise Access to 2-Aroylbenzothiazoles by Redox Condensation Reaction between o-Halonitrobenzenes, Acetophenones, and Elemental Sulfur

Тип публикации: Journal Article

Дата публикации: 2015-05-01

American Chemical Society (ACS)

Organic Letters

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SJR: 1.007

CiteScore: 7.7

Impact factor: 4.7

ISSN: 15237060, 15237052

DOI: 10.1021/acs.orglett.5b01182

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PubMed ID: 25929738

Organic Chemistry

Biochemistry

Physical and Theoretical Chemistry

Краткое описание

A wide range of 2-aroylbenzothiazoles 3 including some pharmacologically relevant derivatives can be obtained in high yields by simply heating o-halonitrobenzenes 1, acetophenones 2, elemental sulfur, and N-methylmorpholine. This three-component nitro methyl coupling was found to occur in an excellent atom-, step-, and redox-efficient manner in which elemental sulfur played the role of nucleophile building block and redox moderating agent to fulfill electronic requirements of the global reaction.

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Nguyen T. B. et al. Concise Access to 2-Aroylbenzothiazoles by Redox Condensation Reaction between o-Halonitrobenzenes, Acetophenones, and Elemental Sulfur // Organic Letters. 2015. Vol. 17. No. 10. pp. 2562-2565.

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Nguyen T. B., Pasturaud K., Ermolenko L., Al-Mourabit A. Concise Access to 2-Aroylbenzothiazoles by Redox Condensation Reaction between o-Halonitrobenzenes, Acetophenones, and Elemental Sulfur // Organic Letters. 2015. Vol. 17. No. 10. pp. 2562-2565.

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TY - JOUR

DO - 10.1021/acs.orglett.5b01182

UR - https://doi.org/10.1021/acs.orglett.5b01182

TI - Concise Access to 2-Aroylbenzothiazoles by Redox Condensation Reaction between o-Halonitrobenzenes, Acetophenones, and Elemental Sulfur

T2 - Organic Letters

AU - Nguyen, Thanh Binh

AU - Pasturaud, Karine

AU - Ermolenko, Ludmila

AU - Al-Mourabit, Ali

PY - 2015

DA - 2015/05/01

PB - American Chemical Society (ACS)

SP - 2562-2565

IS - 10

VL - 17

PMID - 25929738

SN - 1523-7060

SN - 1523-7052

ER -

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@article{2015_Nguyen,

author = {Thanh Binh Nguyen and Karine Pasturaud and Ludmila Ermolenko and Ali Al-Mourabit},

title = {Concise Access to 2-Aroylbenzothiazoles by Redox Condensation Reaction between o-Halonitrobenzenes, Acetophenones, and Elemental Sulfur},

journal = {Organic Letters},

year = {2015},

volume = {17},

publisher = {American Chemical Society (ACS)},

month = {may},

url = {https://doi.org/10.1021/acs.orglett.5b01182},

number = {10},

pages = {2562--2565},

doi = {10.1021/acs.orglett.5b01182}

}

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Nguyen, Thanh Binh, et al. “Concise Access to 2-Aroylbenzothiazoles by Redox Condensation Reaction between o-Halonitrobenzenes, Acetophenones, and Elemental Sulfur.” Organic Letters, vol. 17, no. 10, May. 2015, pp. 2562-2565. https://doi.org/10.1021/acs.orglett.5b01182.

Издатель

American Chemical Society (ACS)

Журнал

Organic Letters

SCImago Q1

Tоп 10% SCImago

WOS Q1

БС1