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[3+2]-Cycloaddition of α-Diazocarbonyl Compounds with Arenediazonium Salts Catalyzed by Silver Nitrate Delivers 2,5-Disubstituted Tetrazoles. / Chuprun, Sergey; Dar'In, Dmitry; Kantin, Grigory; Krasavin, Mikhail.

в: Synthesis (Germany), Том 51, № 21, 2019, стр. 3998-4005.

Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование

Harvard

Chuprun, S, Dar'In, D, Kantin, G & Krasavin, M 2019, '[3+2]-Cycloaddition of α-Diazocarbonyl Compounds with Arenediazonium Salts Catalyzed by Silver Nitrate Delivers 2,5-Disubstituted Tetrazoles', Synthesis (Germany), Том. 51, № 21, стр. 3998-4005. https://doi.org/10.1055/s-0039-1690159

APA

Chuprun, S., Dar'In, D., Kantin, G., & Krasavin, M. (2019). [3+2]-Cycloaddition of α-Diazocarbonyl Compounds with Arenediazonium Salts Catalyzed by Silver Nitrate Delivers 2,5-Disubstituted Tetrazoles. Synthesis (Germany), 51(21), 3998-4005. https://doi.org/10.1055/s-0039-1690159

Vancouver

Chuprun S, Dar'In D, Kantin G, Krasavin M. [3+2]-Cycloaddition of α-Diazocarbonyl Compounds with Arenediazonium Salts Catalyzed by Silver Nitrate Delivers 2,5-Disubstituted Tetrazoles. Synthesis (Germany). 2019;51(21):3998-4005. https://doi.org/10.1055/s-0039-1690159

Author

Chuprun, Sergey ; Dar'In, Dmitry ; Kantin, Grigory ; Krasavin, Mikhail. / [3+2]-Cycloaddition of α-Diazocarbonyl Compounds with Arenediazonium Salts Catalyzed by Silver Nitrate Delivers 2,5-Disubstituted Tetrazoles. в: Synthesis (Germany). 2019 ; Том 51, № 21. стр. 3998-4005.

BibTeX

@article{e15531b1625743b7a23ae87c642b8a60,
title = "[3+2]-Cycloaddition of α-Diazocarbonyl Compounds with Arenediazonium Salts Catalyzed by Silver Nitrate Delivers 2,5-Disubstituted Tetrazoles",
abstract = "[3+2]-Cycloaddition of arenediazonium salts with diazo compounds (earlier exemplified only for trimethylsilyldiazomethane and 2,2,2-trifluorodiazoethane) has been developed to include a wide range of readily available α-diazocarbonyl compounds. The resulting 2-aryl-5-acyl-2 H -tetrazoles are of high value in medicinal chemistry.",
keywords = "arenediazonium tosylates, silver nitrate, tetrazoles, [3+2]-cycloaddition, α-diazocarbonyl compounds, 5-SUBSTITUTED 1H-TETRAZOLES, ACID, ISOCYANIDES, DIAZO-COMPOUNDS, REGIOSELECTIVE 3+2 CYCLOADDITION, MEDICINAL CHEMISTRY, NITRILES, alpha-diazocarbonyl compounds, DIAZOKETONES, INHIBITORS, ACCESS",
author = "Sergey Chuprun and Dmitry Dar'In and Grigory Kantin and Mikhail Krasavin",
year = "2019",
doi = "10.1055/s-0039-1690159",
language = "English",
volume = "51",
pages = "3998--4005",
journal = "Synthesis",
issn = "0039-7881",
publisher = "Georg Thieme Verlag",
number = "21",

}

RIS

TY - JOUR

T1 - [3+2]-Cycloaddition of α-Diazocarbonyl Compounds with Arenediazonium Salts Catalyzed by Silver Nitrate Delivers 2,5-Disubstituted Tetrazoles

AU - Chuprun, Sergey

AU - Dar'In, Dmitry

AU - Kantin, Grigory

AU - Krasavin, Mikhail

PY - 2019

Y1 - 2019

N2 - [3+2]-Cycloaddition of arenediazonium salts with diazo compounds (earlier exemplified only for trimethylsilyldiazomethane and 2,2,2-trifluorodiazoethane) has been developed to include a wide range of readily available α-diazocarbonyl compounds. The resulting 2-aryl-5-acyl-2 H -tetrazoles are of high value in medicinal chemistry.

AB - [3+2]-Cycloaddition of arenediazonium salts with diazo compounds (earlier exemplified only for trimethylsilyldiazomethane and 2,2,2-trifluorodiazoethane) has been developed to include a wide range of readily available α-diazocarbonyl compounds. The resulting 2-aryl-5-acyl-2 H -tetrazoles are of high value in medicinal chemistry.

KW - arenediazonium tosylates

KW - silver nitrate

KW - tetrazoles

KW - [3+2]-cycloaddition

KW - α-diazocarbonyl compounds

KW - 5-SUBSTITUTED 1H-TETRAZOLES

KW - ACID

KW - ISOCYANIDES

KW - DIAZO-COMPOUNDS

KW - REGIOSELECTIVE 3+2 CYCLOADDITION

KW - MEDICINAL CHEMISTRY

KW - NITRILES

KW - alpha-diazocarbonyl compounds

KW - DIAZOKETONES

KW - INHIBITORS

KW - ACCESS

UR - http://www.scopus.com/inward/record.url?scp=85073752880&partnerID=8YFLogxK

U2 - 10.1055/s-0039-1690159

DO - 10.1055/s-0039-1690159

M3 - Article

AN - SCOPUS:85073752880

VL - 51

SP - 3998

EP - 4005

JO - Synthesis

JF - Synthesis

SN - 0039-7881

IS - 21

ER -

ID: 49033698