## Abstract For Abstract see ChemInform Abstract in Full Text.
Intramolecular 1,3-Dipolar Cycloaddition of Azomethine Ylides Generated from Ethoxycarbonylcarbenoids and Schiff Bases.
β Scribed by A. F. Khlebnikov; M. S. Novikov; R. R. Kostikov; J. Kopf
- Publisher
- John Wiley and Sons
- Year
- 2006
- Weight
- 22 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
Abstract
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π SIMILAR VOLUMES
## Abstract Azomethine ylides generated from 5β(alkoxycarbonylmethyl)phenanthridinium cations were studied in 1,3βdipolar cycloadditions with dimethyl maleate and dimethyl fumarate as dipolarophiles. The cycloadducts with the pyrrolidino[1,2βf]phenanthridine skeleton easily underwent dehydrogenatio
## Abstract For Abstract see ChemInform Abstract in Full Text.