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Titanium mediated olefination of aldehydes with α-haloacetates: an exceptionally stereoselective and general approach to (Z)-α-haloacrylates.
Augustine, John Kallikat; Bombrun, Agnes; Venkatachaliah, Srinivasa; Jothi, Anandh.
Affiliation
  • Augustine JK; Syngene International Ltd., Biocon Park, Plot Nos. 2 & 3, Bommasandra IV Phase, Jigani Link Road, Bangalore - 560 099, India. john.kallikat@syngeneintl.com john.kallikat@gmail.com.
Org Biomol Chem ; 11(46): 8065-72, 2013 Dec 14.
Article in En | MEDLINE | ID: mdl-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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Titanium / Acrylates / Aldehydes / Alkenes / Hydrocarbons, Halogenated / Acetates Language: En Journal: Org Biomol Chem Journal subject: BIOQUIMICA / QUIMICA Year: 2013 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Titanium / Acrylates / Aldehydes / Alkenes / Hydrocarbons, Halogenated / Acetates Language: En Journal: Org Biomol Chem Journal subject: BIOQUIMICA / QUIMICA Year: 2013 Document type: Article