The dienolate aldol reaction of (E)-N-crotonoyl C(4)-isopropyl SuperQuat: asymmetric synthesis of α-vinyl-β-hydroxycarboxylic acid derivatives and conversion to α-ethylidene-β-hydroxyesters (β-substituted Baylis–Hillman products)

The synthesis of α-vinyl-β-hydroxyesters and α-ethylidene-β-hydroxyesters (β-substituted Baylis–Hillman products) via the dienolate aldol reaction of (E)-N-crotonoyl C(4)-isopropyl SuperQuat is described. High levels of syn-diastereoselectivity (up to >98% de) are observed for the dienolate aldol reaction with boron enolates, generated either directly with Bu2BOTf or by transmetalation of the potassium enolate with B-bromocatecholborane. Cleavage of the resultant syn-aldol products from the auxiliary gives α-vinyl-β-hydroxyesters in >98% de and >98% ee. Subsequent isomerisation of the double bond into conjugation provides α-ethylidene-β-hydroxyesters (β-substituted Baylis–Hillman products) in high diastereo- and enantiopurity (≥91:9 [(E):(Z)] and >98% ee).

Graphical abstractThe asymmetric dienolate aldol reaction of (E)-N-crotonoyl C(4)-isopropyl SuperQuat provides (after deprotection) α-vinyl-β-hydroxyesters in >98% de and >98% ee. Subsequent double bond isomerisation gives α-ethylidene-β-hydroxyesters in high diastereo- and enantiopurity (≥91:9 [(E)/(Z)] and >98% ee).Figure optionsDownload full-size imageDownload as PowerPoint slide