Multifluorinated Aryl Azides for the Development of Improved H 2 S Probes, and Fast Strain‐promoted Azide‐Alkyne Cycloaddition and Staudinger Reactions-Reference-Cited by-同舟云学术

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Multifluorinated Aryl Azides for the Development of Improved H 2 S Probes, and Fast Strain‐promoted Azide‐Alkyne Cycloaddition and Staudinger Reactions

Published:2020-03-23 Issue:9 Volume:15 Page:1420-1429
ISSN:1861-4728
Container-title:Chemistry – An Asian Journal
language:en
Short-container-title:Chem. Asian J.

Author:

Kang Xueying¹,Cai Xuekang¹,Yi Long¹²^ORCID,Xi Zhen³²

Affiliation:

1. State Key Laboratory of Organic-Inorganic Composites and Beijing Key Lab of BioprocessBeijing University of Chemical Technology (BUCT) 15 Beisanhuan East Road Beijing 100029 China

2. Collaborative Innovation Center of Chemical Science and Engineering Tianjin 300072 China

3. State Key Laboratory of Elemento-Organic Chemistry and Department of Chemical Biology National Pesticide Engineering Research Center (Tianjin)Nankai University 94 Weijin Road Tianjin 300071 China

Funder

National Natural Science Foundation of China

Natural Science Foundation of Beijing Municipality

Publisher

Wiley

Subject

General Chemistry,Biochemistry,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/asia.202000005

Reference143 articles.

1. XVIII. On a new series of bodies in which nitrogen substituted for hydrogen

2.

3. Azides: their preparation and synthetic uses

4. Alkyl and Aryl Azides.

5. Organic Azides: An Exploding Diversity of a Unique Class of Compounds

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