Chemical Communications

, volume 52 , issue 99 , pages 14188-14199

Regioselective synthesis of multisubstituted 1,2,3-triazoles: moving beyond the copper-catalyzed azide–alkyne cycloaddition

Fang Wei ¹

Weiguo Wang ¹

Yudao Ma ¹

Chen-Ho Tung ¹

Zhenghu Xu ^{1, 2}

Hide authors affiliations Show authors affiliations: 2 affiliations

Key Lab of Colloid and Interface Chemistry of Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, No. 27 South Shanda Road, Jinan, Shandong 250100, China |

State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, shanghai 200032, P. R. China |

Publication type: Journal Article

Publication date: 2016-09-26

Royal Society of Chemistry (RSC)

Chemical Communications

scimago Q1

wos Q2

SJR: 1.037

CiteScore: 7.4

Impact factor: 4.2

ISSN: 13597345, 1364548X

DOI: 10.1039/C6CC06194J

Copy DOI

PubMed ID: 27711308

Materials Chemistry

Metals and Alloys

Surfaces, Coatings and Films

General Chemistry

Ceramics and Composites

Electronic, Optical and Magnetic Materials

Catalysis

Abstract

Copper(i)-catalyzed azide–alkyne cycloaddition (CuAAC) provides an efficient synthesis of 1,4-disubstituted 1,2,3-triazoles. This feature article highlights the recent progress on the regisoselective synthesis of multisubstituted 1,2,3-triazoles, which current click reaction (CuAAC) is unable to do.

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GOST |

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GOST Copy

Wei F. et al. Regioselective synthesis of multisubstituted 1,2,3-triazoles: moving beyond the copper-catalyzed azide–alkyne cycloaddition // Chemical Communications. 2016. Vol. 52. No. 99. pp. 14188-14199.

GOST all authors (up to 50) Copy

Wei F., Wang W., Ma Y., Tung C., Xu Z. Regioselective synthesis of multisubstituted 1,2,3-triazoles: moving beyond the copper-catalyzed azide–alkyne cycloaddition // Chemical Communications. 2016. Vol. 52. No. 99. pp. 14188-14199.

RIS |

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RIS Copy

TY - JOUR

DO - 10.1039/C6CC06194J

UR - https://doi.org/10.1039/C6CC06194J

TI - Regioselective synthesis of multisubstituted 1,2,3-triazoles: moving beyond the copper-catalyzed azide–alkyne cycloaddition

T2 - Chemical Communications

AU - Wei, Fang

AU - Wang, Weiguo

AU - Ma, Yudao

AU - Tung, Chen-Ho

AU - Xu, Zhenghu

PY - 2016

DA - 2016/09/26

PB - Royal Society of Chemistry (RSC)

SP - 14188-14199

IS - 99

VL - 52

PMID - 27711308

SN - 1359-7345

SN - 1364-548X

ER -

BibTex |

Cite this

BibTex (up to 50 authors) Copy

@article{2016_Wei,

author = {Fang Wei and Weiguo Wang and Yudao Ma and Chen-Ho Tung and Zhenghu Xu},

title = {Regioselective synthesis of multisubstituted 1,2,3-triazoles: moving beyond the copper-catalyzed azide–alkyne cycloaddition},

journal = {Chemical Communications},

year = {2016},

volume = {52},

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

month = {sep},

url = {https://doi.org/10.1039/C6CC06194J},

number = {99},

pages = {14188--14199},

doi = {10.1039/C6CC06194J}

}

MLA

Cite this

MLA Copy

Wei, Fang, et al. “Regioselective synthesis of multisubstituted 1,2,3-triazoles: moving beyond the copper-catalyzed azide–alkyne cycloaddition.” Chemical Communications, vol. 52, no. 99, Sep. 2016, pp. 14188-14199. https://doi.org/10.1039/C6CC06194J.

Publisher

Royal Society of Chemistry (RSC)

Journal

Chemical Communications

scimago Q1

wos Q2

SJR

1.037

CiteScore

7.4

Impact factor

4.2

ISSN

13597345 (Print)

1364548X (Electronic)

Profiles

Chen-Ho F Tung