Standard

5-Iodo-1H-1,2,3-triazoles as Versatile Building Blocks. / Danilkina, Natalia A.; Govdi, Anastasia I.; Balova, Irina A.

в: Synthesis, Том 52, № 13, 01.07.2020, стр. 1874–1896.

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

Harvard

Danilkina, NA, Govdi, AI & Balova, IA 2020, '5-Iodo-1H-1,2,3-triazoles as Versatile Building Blocks', Synthesis, Том. 52, № 13, стр. 1874–1896. https://doi.org/10.1055/s-0039-1690858

APA

Danilkina, N. A., Govdi, A. I., & Balova, I. A. (2020). 5-Iodo-1H-1,2,3-triazoles as Versatile Building Blocks. Synthesis, 52(13), 1874–1896. https://doi.org/10.1055/s-0039-1690858

Vancouver

Danilkina NA, Govdi AI, Balova IA. 5-Iodo-1H-1,2,3-triazoles as Versatile Building Blocks. Synthesis. 2020 Июль 1;52(13):1874–1896. https://doi.org/10.1055/s-0039-1690858

Author

Danilkina, Natalia A. ; Govdi, Anastasia I. ; Balova, Irina A. / 5-Iodo-1H-1,2,3-triazoles as Versatile Building Blocks. в: Synthesis. 2020 ; Том 52, № 13. стр. 1874–1896.

BibTeX

@article{faa327a0b54449da8d55ce1dbca5e3d0,
title = "5-Iodo-1H-1,2,3-triazoles as Versatile Building Blocks",
abstract = "Copper-catalyzed azide–alkyne cycloaddition is a useful tool for the synthesis of both 1,2,3-triazoles and 5-iodo-1H-1,2,3-triazoles starting from either terminal alkynes or iodoalkynes. 5-Iodotriazoles have been recognized as very useful building blocks for the synthesis of diverse 1,4,5-trisubstituted 1,2,3-triazoles. Synthetic application of 5-iodo-1,2,3-triazoles through the creation of a new C–C, C–heteroatom, or C–D(T) bond along with the application areas of both iodotriazoles and products of their modification including radiolabeled compounds are discussed.",
keywords = "CuAAC, 5-iodo-1,2,3-triazoles, iodoacetylenes, cross-coupling, hetero-coupling, halogen exchange, radiolabeling, ONE-POT REACTION, ORGANIC AZIDES, SUBSTITUTED 1,2,3-TRIAZOLES, ALKYNE, CROSS-COUPLING REACTIONS, IN-VITRO, 1,3-DIPOLAR CYCLOADDITION, REGIOSELECTIVE SYNTHESIS, CLICK-CHEMISTRY, METAL-FREE",
author = "Danilkina, {Natalia A.} and Govdi, {Anastasia I.} and Balova, {Irina A.}",
note = "Publisher Copyright: {\textcopyright} 2020 Georg Thieme Verlag. All rights reserved.",
year = "2020",
month = jul,
day = "1",
doi = "10.1055/s-0039-1690858",
language = "English",
volume = "52",
pages = "1874–1896",
journal = "Synthesis",
issn = "0039-7881",
publisher = "Georg Thieme Verlag",
number = "13",

}

RIS

TY - JOUR

T1 - 5-Iodo-1H-1,2,3-triazoles as Versatile Building Blocks

AU - Danilkina, Natalia A.

AU - Govdi, Anastasia I.

AU - Balova, Irina A.

N1 - Publisher Copyright: © 2020 Georg Thieme Verlag. All rights reserved.

PY - 2020/7/1

Y1 - 2020/7/1

N2 - Copper-catalyzed azide–alkyne cycloaddition is a useful tool for the synthesis of both 1,2,3-triazoles and 5-iodo-1H-1,2,3-triazoles starting from either terminal alkynes or iodoalkynes. 5-Iodotriazoles have been recognized as very useful building blocks for the synthesis of diverse 1,4,5-trisubstituted 1,2,3-triazoles. Synthetic application of 5-iodo-1,2,3-triazoles through the creation of a new C–C, C–heteroatom, or C–D(T) bond along with the application areas of both iodotriazoles and products of their modification including radiolabeled compounds are discussed.

AB - Copper-catalyzed azide–alkyne cycloaddition is a useful tool for the synthesis of both 1,2,3-triazoles and 5-iodo-1H-1,2,3-triazoles starting from either terminal alkynes or iodoalkynes. 5-Iodotriazoles have been recognized as very useful building blocks for the synthesis of diverse 1,4,5-trisubstituted 1,2,3-triazoles. Synthetic application of 5-iodo-1,2,3-triazoles through the creation of a new C–C, C–heteroatom, or C–D(T) bond along with the application areas of both iodotriazoles and products of their modification including radiolabeled compounds are discussed.

KW - CuAAC

KW - 5-iodo-1,2,3-triazoles

KW - iodoacetylenes

KW - cross-coupling

KW - hetero-coupling

KW - halogen exchange

KW - radiolabeling

KW - ONE-POT REACTION

KW - ORGANIC AZIDES

KW - SUBSTITUTED 1,2,3-TRIAZOLES

KW - ALKYNE

KW - CROSS-COUPLING REACTIONS

KW - IN-VITRO

KW - 1,3-DIPOLAR CYCLOADDITION

KW - REGIOSELECTIVE SYNTHESIS

KW - CLICK-CHEMISTRY

KW - METAL-FREE

UR - http://www.scopus.com/inward/record.url?scp=85087046552&partnerID=8YFLogxK

UR - https://www.mendeley.com/catalogue/218aaf55-af33-31d0-898c-ee9813b803e5/

U2 - 10.1055/s-0039-1690858

DO - 10.1055/s-0039-1690858

M3 - Review article

VL - 52

SP - 1874

EP - 1896

JO - Synthesis

JF - Synthesis

SN - 0039-7881

IS - 13

ER -

ID: 54236200