91660-91-2Relevant academic research and scientific papers
ENOLBORONATES: NEW PRACTICAL REAGENTS FOR REGIOSELECTIVE ALDOL CONDENSATIONS.
Gennari, Cesare,Colombo, Lino,Poli, Giovanni
, p. 2279 - 2282 (1984)
Enolboronates, new enolates directly accessible from carbonyl compounds and giving aldol products regioselectively and in good yield with aliphatic and aromatic aldehydes, are described.
A New Protocol for Regio- and Stereocontrolled Aldol Reactions through the Conjugate Addition of Dialkylboranes to α,β-Unsaturated Ketones
Boldrini, Gian Paolo,Bortolotti, Michele,Mancini, Fabrizio,Tagliavini, Emilio,Trombini, Claudio,Umani-Ronchi, Achille
, p. 5820 - 5826 (2007/10/02)
A one-pot, two-step procedure, consisting of the 1,4-addition of dialkylboranes to β-substituted (E)-α,β-unsaturated ketones followed by the reaction of the resulting configurationally pure (Z)-(vinyloxy)boranes with aldehydes, is reported.The overall process corresponds to a regio- and stereocontrolled aldol addition of an unsymmetrical ketone to an aldehyde.A concerted 1,4-addition mechanism accounts for the stereochemical outcome of the hydroboration reaction; cyclic enones do not undergo conjugate addition, while (Z)-β-substituted or β,β-disubstituted α,β-unsaturated ketones still react in a 1,4-fashion, but with a slower rate and a lower degree of chemoselectivity with respect to β-substituted (E)-α,β-unsaturated ketones.In the cases of α,β-disubstituted α,β-unsaturated ketones and (E)-(S-phenylthio)cinnamate, which react with dicyclohexylborane to give a mixture of E and Z enolates, an alternative mechanism is proposed.
