بازدید:41538 بروزرسانی: 10-11-1402
Ali Ramazani, Ebrahim Ahmadi and Nader Noshiranzadeh
Stereoselective Synthesis of Dialkyl 1,1-diacetyl-8a-hydroxy-8-oxo-1,2,8,8atetrahydrocyclopenta[ a]indene-2,3-dicarboxylates from the Reaction of Dialkyl 2-(1-acetyl-2- oxopropyl)-3-(tributylphosphoranylidene) Succinates with Indene-1,2,3-trione |
Protonation of the highly reactive 1 : 1 intermediates produced in the reaction between tributylphosphine and dialkyl acetylenedicarboxylates by acetylacetone leads to sterically congested phosphorus ylides. Reaction between the sterically congested phosphorus ylides with ninhydrin leads to stereoselective synthesis of dialkyl 1,1-diacetyl-8a-hydroxy-8-oxo-1,2,8,8a-tetrahydrocyclopenta[a]indene-2,3-carboxylates in the presence of magnesium sulfate powder in solvent-free conditions. |