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Title: Effect of ester on rhodium-catalyzed intermolecular [5+2] cycloaddition of 3-acyloxy-1,4-enynes and alkynes. Author: Schienebeck CM, Robichaux PJ, Li X, Chen L, Tang W. Journal: Chem Commun (Camb); 2013 Apr 04; 49(26):2616-8. PubMed ID: 23435501. Abstract: We systematically examined the effect of different esters on the rhodium-catalyzed intermolecular [5+2] cycloaddition of 3-acyloxy-1,4-enynes and alkynes with a concomitant 1,2-acyloxy migration. Significant rate acceleration was observed for benzoate substrates bearing an electron-donating substituent. The cycloaddition can now be conducted under much more practical conditions for most terminal alkynes.[Abstract] [Full Text] [Related] [New Search]