Chiral Primary Amine/Ketone Cooperative Catalysis for Asymmetric α-Hydroxylation with Hydrogen Peroxide

<p>Carbonyl and amine are yin and yang in organocatalysis that mutually activate and transform each other. As intrinsically reacting partners, carbonyl and amine tend to condensate, depleting their individual activity when employed as catalysts. Though widely established as prominent catalytic strategies, aminocatalysis and carbonyl catalysis seems not coexist well and a cooperative amine/carbonyl dual catalysis remains virtually unknown. Here we report a cooperative primary amine and ketone dual catalysis in the asymmetric <i>α</i>-hydroxylation with H₂O₂. Besides participating in the typical enamine catalytic cycle, the chiral primary amine catalyst was found to work cooperatively with a ketone catalyst to activate H₂O₂ <i>via</i> an oxaziridine intermediate derived from<i> in-situ</i> generated ketimine intermediate. The resulted enamine-oxaziridine coupling then facilitated highly-controlled hydroxylation of <i>β</i>-ketocarbonyls that are not possible with other catalytic methods. The dual catalytic approach allows for highly enantioselective <i>α</i>-hydroxylation of a broad range of <i>β</i>-ketocarbonyls. Particularly, late-stage hydroxylation for peptidyl amide or chiral esters can also be achieved with high stereoselectivity. With its operational simplicity and mild conditions, this cooperative amine/ketone catalysis provides a new strategy in catalytic activation of H₂O₂ and expands the domain of typical amine and carbonyl catalysis to include those challenging transformations.</p>

Chiral Primary Amine/Ketone Cooperative Catalysis for Asymmetric α-Hydroxylation with Hydrogen Peroxide

<p>Carbonyl and amine are yin and yang in organocatalysis that mutually activate and transform each other. As intrinsically reacting partners, carbonyl and amine tend to condensate, depleting their individual activity when employed as catalysts. Though widely established as prominent catalytic strategies, aminocatalysis and carbonyl catalysis seems not coexist well and a cooperative amine/carbonyl dual catalysis remains virtually unknown. Here we report a cooperative primary amine and ketone dual catalysis in the asymmetric <i>α</i>-hydroxylation with H₂O₂. Besides participating in the typical enamine catalytic cycle, the chiral primary amine catalyst was found to work cooperatively with a ketone catalyst to activate H₂O₂ <i>via</i> an oxaziridine intermediate derived from<i> in-situ</i> generated ketimine intermediate. The resulted enamine-oxaziridine coupling then facilitated highly-controlled hydroxylation of <i>β</i>-ketocarbonyls that are not possible with other catalytic methods. The dual catalytic approach allows for highly enantioselective <i>α</i>-hydroxylation of a broad range of <i>β</i>-ketocarbonyls. Particularly, late-stage hydroxylation for peptidyl amide or chiral esters can also be achieved with high stereoselectivity. With its operational simplicity and mild conditions, this cooperative amine/ketone catalysis provides a new strategy in catalytic activation of H₂O₂ and expands the domain of typical amine and carbonyl catalysis to include those challenging transformations.</p>

Rhodium-catalyzed asymmetric synthesis of β-branched esters from allylic amines

β-Substituted chiral esters are synthesized in excellent yields and enantioselectivities from allylic amines using [(BINAP)Rh]BArF4 as the chiral catalyst.