Moderating Strain without Sacrificing Reactivity: Design of Fast and Tunable Noncatalyzed Alkyne–Azide Cycloadditions via Stereoelectronically Controlled Transition State Stabilization-Reference-Cited by-同舟云学术

Moderating Strain without Sacrificing Reactivity: Design of Fast and Tunable Noncatalyzed Alkyne–Azide Cycloadditions via Stereoelectronically Controlled Transition State Stabilization

Published:2013-01-15 Issue:4 Volume:135 Page:1558-1569
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Gold Brian¹,Dudley Gregory B.¹,Alabugin Igor V.¹

Affiliation:

1. Department of Chemistry and Biochemistry, Florida State University, Tallahassee, Florida, 32306-4390, United States

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja3114196

Reference111 articles.

1. Click Chemistry: Diverse Chemical Function from a Few Good Reactions

2. Front cover

3. Click chemistry reactions in medicinal chemistry: Applications of the 1,3-dipolar cycloaddition between azides and alkynes

4. Cu-free click cycloaddition reactions in chemical biology

5. Visualizing Metabolically Labeled Glycoconjugates of Living Cells by Copper-Free and Fast Huisgen Cycloadditions

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