Verma, Naimish K. published the artcileRegioselective Synthesis of 1,4,5-Trisubstituted 1,2,3-Triazole Derivatives from α,β-Unsaturated Carbonyls, Computed Properties of 143-15-7, the publication is European Journal of Organic Chemistry (2022), 2022(28), e202200317, database is CAplus.
The copper-catalyzed oxidative azide-olefin cycloaddition (OAOC) reaction of differently substituted α,β-unsaturated carbonyls with azides provided an efficient method for preparing biol. active 1,4,5-trisubstituted 1,2,3-triazoles. In this study, the cycloaddition reaction was found to be a simple and powerful method for constructing diverse mono- and bis-(1,4,5-trisubstituted 1,2,3-triazole) functionalized heterocyclic compounds in moderate to high yields with great regioselectivity. The XRD-anal. data of one of the bis-triazole derivatives supported the regioselectivity as well as the conformity of the method in the construction of the triazole nucleus. The preliminary antifungal profile against C. albicans was observed with cinnamaldehyde-based triazole derivatives demonstrating promising results.
European Journal of Organic Chemistry published new progress about 143-15-7. 143-15-7 belongs to bromides-buliding-blocks, auxiliary class Bromide,Aliphatic hydrocarbon chain, name is 1-Bromododecane, and the molecular formula is C23H43NP2, Computed Properties of 143-15-7.
Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary