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1,3-Dipolar Cycloadditions of Fulminic Acid

✍ Scribed by Prof. R. Huisgen; Dipl.-Chem. M. Christl


Publisher
John Wiley and Sons
Year
1967
Tongue
English
Weight
218 KB
Volume
6
Category
Article
ISSN
0044-8249

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## Abstract Azomethine ylides generated from 5‐(alkoxycarbonylmethyl)phenanthridinium cations were studied in 1,3‐dipolar cycloadditions with dimethyl maleate and dimethyl fumarate as dipolarophiles. The cycloadducts with the pyrrolidino[1,2‐f]phenanthridine skeleton easily underwent dehydrogenatio