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1,3-Dipolar Cycloaddition of Azomethine Ylides Generated from Schiff Bases and Difluorocarbene to Symmetric Olefins

โœ Scribed by M. S. Novikov; A. F. Khlebnikov; E. S. Sidorina; A. E. Masalev; J. Kopf; R. R. Kostikov


Book ID
110390038
Publisher
SP MAIK Nauka/Interperiodica
Year
2002
Tongue
English
Weight
115 KB
Volume
38
Category
Article
ISSN
1070-4280

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๐Ÿ“œ SIMILAR VOLUMES


Intramolecular 1,3-Dipolar Cycloaddition
โœ A. F. Khlebnikov; M. S. Novikov; R. R. Kostikov; J. Kopf ๐Ÿ“‚ Article ๐Ÿ“… 2006 ๐Ÿ› John Wiley and Sons โš– 22 KB ๐Ÿ‘ 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.

Generation and 1,3-dipolar cycloaddition
โœ Mikhail S. Novikov; Alexander F. Khlebnikov; Alexander E. Masalev; Rafael R. Kos ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 279 KB

Iminiodiflouromethanides, generated by the reaction of difluorocarbene with Nbenzylidene amines, undergo 1,3-dipolar cycloaddition to electron-deficient alkenes to give pyrrolidine derivatives in moderate to good yields.