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
## 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