Navigation

0 Hits

  • Previous / Next

You are using Science Of Synthesis as a Guest.
Please login to access the full content or check if you have access via
18.6.6.1.2.4 Method 4: Palladium-Catalyzed Reaction of 2-Vinylthiiranes with Isocyanates

DOI: 10.1055/sos-SD-018-00578

Rossi, L.Science of Synthesis, (200518627.

The palladium-catalyzed ring expansion of 2-vinylthiiranes with isocyanates affords thiazolidin-2-ones, e.g. 339, in moderate yields (Scheme 243). The reaction is catalyzed by a tris(dibenzylideneacetone)dipalladiumchloroform complex in the presence of a bidentate phosphine ligand.[‌558‌]

Meeeee 888 Meeeeeeee-Meeeeeeee Meeeeeee ee 8-Meeeeeeeeeeeee eeee Meeeeeeeeee[‌888‌]

Meeeeeeeeeee Meeeeeeee

8-(8-Meeeeeeeeeee)-8-eeeee-8,8-eeeeeeeeeee-8-eee (888); Meeeeee Meeeeeeee:[‌888‌]

M eeeeeee ee eee Me eeeeeeee (8.88eeee), eeeeeeeee eeeeee (8.88eeee), eee MMM (8eM) eee eeeeeee eeeee M8 eeeeeeeeee ee e eeeee eeeeeeeee ee ee eee 88eee. 8-Meeeeeeeeeeee (8eeee), 8-eeeeee-8-eeeeeeeeeeeeeeeee (8.8eeee), eee MMM (8eM) eeee eeeee, eee eee eeeeeee eee eeeeeee eeeee M8 (888Meee) ee 88°M eee 88e (eee eeeeeeeeee ee eee eeeeeeeeee eee eeeeeeeee ee MM). Mee eeeeeee eee eeeeeeee eeeeeee Meeeee eee eeeeeeeeeeee. Mee eeeeeee eee eeeeeeee ee eeeeeeeeeee MMM (eeeeeee/Me8M) ee eeee eee eeeeeee ee ee eeee eeeeee; eeeee: 88%; MM (ν̃): 8888ee8; 8MMMM (888MMe, MMMe8, δ): 8.88 (ee, 8M), 8.88 (ee, 8M), 8.88 (e, 8M), 8.88 (e, 8M).

References


Cookie-Einstellungen