131897-91-1Relevant academic research and scientific papers
Anti-Selective enolboration-aldolization of propanoic acid
Ramachandran, P. Veeraraghavan,Chanda, Prem B.,Otoo, Barnabas
supporting information, p. 1289 - 1291 (2014/03/21)
A systematic examination of enolboration-aldolization of propanoic acid has led to an efficient synthesis of anti-β-hydroxy-α-methyl carboxylic acids in consistently high yields and diastereoselectivities by using B-bromodicyclohexylborane as the enolizat
DIRECT, ENANTIOSELECTIVE ALDOL COUPLING OF ALDEHYDES USING CHIRAL ORGANIC CATALYSTS
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Page/Page column 22-23, (2008/06/13)
Nonmetallic, chiral organic catalysts are used to catalyze an enantioselective aldol coupling reaction between aldehyde substrates. The reaction may be carried out with a single enolizable aldehyde, resulting in dimerization to give a β-hydroxy aldehyde,
REGIOSELECTIVE OPENINGS OF 2,3-EPOXY ACIDS WITH ORGANOCUPRATES
Chong, J. Michael,Sharpless, K. Barry
, p. 4683 - 4686 (2007/10/02)
Lithium organocuprates react with 3-alkyl-2,3-epoxy acids (glycidic acids) to afford the products of ring-opening in good yield.The regiochemistry of ringopening is dependent on the stereochemistry of the epoxy acid.
