𝔖 Bobbio Scriptorium
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1,3-Dipolar cycloaddition of diazocompounds to 1-alkenylboronic esters

✍ Scribed by Mohammed Jazouli; Bertrand Carboni; Robert Carrié; Mohammed Soufiaoui; Loïc Toupet


Book ID
102228874
Publisher
John Wiley and Sons
Year
1994
Tongue
English
Weight
488 KB
Volume
5
Category
Article
ISSN
1042-7163

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✦ Synopsis


A variety of diazo compounds was added to the parent vinylboronic ester derived from pinacol. The reactivity of some substituted I -alkenylboronic esters is also briefly examined. The nonisolated primary adducts spontaneously rearrange via a I ,3-boron migration and lead to I -borylated-2-pyrazolines. The structure of one of these compounds has been established by X-ray difiaction analysis.


📜 SIMILAR VOLUMES


1,3-Dipolar cycloadditions to alkyldicya
✍ P. H. Benders; D. N. Reinhoudt; D. M. W. van den Ham 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 413 KB

## Abstract The 1,3‐dipoles 2,4,6‐trimethylbenzonitrile oxide and benzyl azide react with alkyldicyanamides (**1**) to give the 3,5‐disubstituted 1,2,4‐oxadiazoles **2** and the 1,5‐disubstituted tetrazole **4**, respectively, by (3 + 2)‐cycloaddition. The structure of 4 has been determined by a si