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An efficient dipolar-cycloaddition route to the pterosin family of sesquiterpenes

✍ Scribed by Erin A. Curtis; Vincent P. Sandanayaka; Albert Padwa


Publisher
Elsevier Science
Year
1995
Tongue
French
Weight
175 KB
Volume
36
Category
Article
ISSN
0040-4039

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πŸ“œ SIMILAR VOLUMES


1,3-Dipolar cycloaddition of stabilized
✍ Abdelmalek Bouraiou; Abdelmadjid Debache; Salah Rhouati; Ali Belfaitah; Bertrand πŸ“‚ Article πŸ“… 2008 πŸ› Journal of Heterocyclic Chemistry 🌐 English βš– 281 KB

## Abstract magnified image Some new polysubstituted 3‐pyrrolidinylquinolinyl derivatives were prepared by 1,3 dipolar cycloadditions of an azomethine ylide, generated __in situ__ from benzylideneimine of methylglycinate and triethylamine in the presence of LiBr, to quinolyl Ξ±,β‐unsaturated esters