Click chemistry is a term coined by Barry Sharpless to describe chemical reactions that are modular, efficient, broadly applicable, high yield, and free of harmful by-products. The best-known example of a "click" reaction is the copper(I)-catalyzed azide-alkyne 1,3-dipolar cycloaddition (CuAAC), which leads to 1,4-disubstituted penta-membered 1,2, 3-triazole ring.
Click chemistry
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- N-(1R,8S,9s)-Bicyclo[6.1.0]non-4-yn-9-ylmethyloxycarbonyl-1,8-diamino-3,6-dioxaoctane
Cas#:1263166-93-3
Starting at $219.90
- 2,2,6,6-Tetramethyl-4-(2-propynyloxy)piperidine 1-Oxyl Free Radical
Cas#:147045-24-7
Starting at $25.90
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![N-(1R,8S,9s)-Bicyclo[6.1.0]non-4-yn-9-ylmethyloxycarbonyl-1,8-diamino-3,6-dioxaoctane](https://media-prod.aladdinsci.com/media/catalog/product/cache/5a65292c9ea620f6e55f72f0a2fa59fb/n/1/n159029.png)
