## Abstract For Abstract see ChemInform Abstract in Full Text.
Hetero-1,3-dipolar cycloadditions of dithiolane-isocyanate imminium methylides: A novel route to 1,3-oxazolidine- and thiazolidine-2-thiones
โ Scribed by Colin W.G. Fishwick; Richard J. Foster; Robin E. Carr
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- French
- Weight
- 168 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
The 1,3-cycloadditions of thione S-methylides 2 and 9 to dimethyl 2,3\_dicyanofumarate and 2,3\_dicyanomaleate are nonstere5speciFi.c. A preceding cis,trans isomerization of the unsaturated dipolarophiles catalyzed by the thiadiazolines (precursors of the thione S-methylides) had to be suppressed in
A Novel and Effective Route to 1,3-Oxazolidine Derivatives. Palladium-Catalyzed Regioselective [3 + 2] Cycloaddition of Vinylic Oxiranes with Imines. -The present palladium-catalyzed intermolecular regioselective [3 + 2] cycloaddition of imines (I) with vinylic oxiranes (II) is a new version of 1,3