148902-19-6Relevant articles and documents
Cycloaddition chemistry of anhydro-4-hydroxy-1,3-thiazolium hydroxides (thioisomunchnones) for the synthesis of heterocycles
Padwa,Harring,Hertzog,Nadler
, p. 993 - 1004 (2007/10/02)
A series of α,α-disubstituted thioisomunchnones were prepared by treating acyclic or cyclic thioamides with bromoacetyl chloride in the presence of triethylamine. The resulting mesoionic dipole was found to undergo bimolecular 1,3-dipolar cycloaddition wi
RHODIUM(II) CATALYZED CYCLIZATION OF DIAZO THIOCARBONYL COMPOUNDS FOR HETEROCYCLIC SYNTHESIS
Padwa, Albert,Kinder, Frederic R.,Nadler, William R.,Zhi, Lin
, p. 367 - 383 (2007/10/02)
The mesoionic thioisomuenchnone system was prepared from the rhodium(II) acetate catalyzed cyclization of a diazothioamide and was found to undergo smooth 1,3-dipolar cycloaddition with N-phenylmaleimide.In contrast to this system, the rhodium(II) reaction of α-diazo-β-oxo ester containing a thiocarbonyl group produced a cyclic thiocarbonyl ylide which extruded sulfur from a transient episulfide intermediate.