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Search results with tag "Enolates"

Ch. 7 - Enolates - Purdue University

Ch. 7 - Enolates - Purdue University

www.chem.purdue.edu

651.06 209 Enolates Enolates are the conjugate anions of carbonyl compounds. Although they have been known and used since the turn of the 20th Century, it was the development of “specific enolates” (see below) by H. O. House of MIT in the 1960-1970s that made carbanion

  7 enolates, Enolates

O O E+ E - University of Texas at Dallas

O O E+ E - University of Texas at Dallas

www.utdallas.edu

Enols and Enolates! A type of reaction with carbonyl compounds is an α-substitution! (an electrophile adds to the α carbon of a carbonyl)! O O

  University, Lone, Texas, Dallas, University of texas at dallas, Enolates, Enols and enolates

123.312 Advanced Organic Chemistry: Retrosynthesis

123.312 Advanced Organic Chemistry: Retrosynthesis

www.massey.ac.nz

CO2H FGI hydrolysis CO2Et C=C CO2Et CHO CO2Et PPh3 The second is probably the hardest; there is no simple enolate disconnections so we have to look slightly further a field.

  Enolates

O NUC O H C CH H C CH NUC O - The University of Texas at ...

O NUC O H C CH H C CH NUC O - The University of Texas at ...

utdallas.edu

Reactions at α-Position! 2) To make a carbonyl compound even more nucleophilic at the α-position, ! a base can be added to form an enolate! H3C O

  Enolates

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