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Title: Titanium mediated olefination of aldehydes with α-haloacetates: an exceptionally stereoselective and general approach to (Z)-α-haloacrylates. Author: Augustine JK, Bombrun A, Venkatachaliah S, Jothi A. Journal: Org Biomol Chem; 2013 Dec 14; 11(46):8065-72. PubMed ID: 24145668. Abstract: An exceptionally stereoselective and general synthesis of (Z)-α-haloacrylates, ready to undergo various synthetic transformations, has been demonstrated from α-haloacetates and aldehydes in a one-pot manner via the titanium-enolate based asymmetric aldol condensation. Besides being an expedient synthetic procedure, the ready availability of diverse α-haloacetates, exceptional stereoselectivity, and high yields make the process a versatile transformation in organic synthesis. The potential of this method in up-scaling operations has been illustrated.[Abstract] [Full Text] [Related] [New Search]