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Kinetics and mechanism of 1,3-cycloaddition of a substituted benzonitrile oxide to a series of arylacetylenes

✍ Scribed by Beltrame, P.; Veglio, C.; Simonetta, M.

Book ID
121306405
Publisher
Royal Society of Chemistry
Year
1967
Weight
1019 KB
Category
Article
ISSN
0045-6470

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1,3-Dipolar Cycloaddition of Benzonitril
1,3-Dipolar Cycloaddition of Benzonitrile Oxide to Substituted 4,5-Dihydro-3-methylene-2(3H)-furanones
✍ Štverková, Slávka ;Žák, Zdirad ;Jonas, Jaroslav 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 English ⚖ 462 KB

## Abstract Benzonitrile oxide cycloadds to the CC bond of substituted 4,5‐dihydro‐3‐methylene‐2(3__H__)‐furanones 1a–1g. Thus, (__E__)‐1a and (__E__)‐1b are converted into the corresponding isoxazolinespirodihydrofuranones (4__RS__,5__RS__)‐2a and (4__RS__,5__RS__)‐2b, and (__E__)‐1c is converted