Oxonium ylides were formed via an intramolecular reaction between a series of dioxalanes and metallocarbenes. The substitution patterns present in the ketals greatly affect the rearrangements of the oxonium ylides. It was also demonstrated that electron-deficient copper (II) species are superior catalysts for these systems
Despite the importance of allylic ylide rearrangements for the synthesis of complex molecules, the c...
The first computational study of the rearrangement reactions of oxiranes initiated by lithium dialky...
Synthetically useful α,β-unsaturated carbonyl compounds were obtained from gold-catalyzed oxidative ...
Oxonium ylides were formed via an intramolecular reaction between a series of dioxalanes and metallo...
Intramolecular exposure of cyclic ketals to metal carbenoids generates a proposed oxonium ylide inte...
A series of ketal-containing diazocarbonyl substrates was prepared. Exposure of these substrates to ...
The axial–equatorial conformational isomer distribution of the reactant diazoacetoacetate or its met...
The variety of α-diazo β-keto esters (3a-f, 8a-f) with varying substituents (ED/EW) on the...
Rh(II)-catalyzed oxonium ylide formation–[2,3] sigmatropic rearrangement of α-diazo-β-ketoesters po...
Rhodium-, copper- and iridium-catalyzed reactions of the <sup>13</sup>C-labelled diazo c...
Detailed in this account are our efforts toward efficient oxacycle syntheses. Two complementary appr...
We have developed catalyst-controlled regiodivergent rearrangements of onium-ylides derived from ind...
The synthesis and rearrangements of the chiral carbinols 8 and 9 are described. With KH-THF. both th...
Summary: Metal carbenes, divalent carbon species, are versatile intermediates that enable novel synt...
l,2-Dioxines are an important class of compounds that are useful in organic synthesis for the incorp...
Despite the importance of allylic ylide rearrangements for the synthesis of complex molecules, the c...
The first computational study of the rearrangement reactions of oxiranes initiated by lithium dialky...
Synthetically useful α,β-unsaturated carbonyl compounds were obtained from gold-catalyzed oxidative ...
Oxonium ylides were formed via an intramolecular reaction between a series of dioxalanes and metallo...
Intramolecular exposure of cyclic ketals to metal carbenoids generates a proposed oxonium ylide inte...
A series of ketal-containing diazocarbonyl substrates was prepared. Exposure of these substrates to ...
The axial–equatorial conformational isomer distribution of the reactant diazoacetoacetate or its met...
The variety of α-diazo β-keto esters (3a-f, 8a-f) with varying substituents (ED/EW) on the...
Rh(II)-catalyzed oxonium ylide formation–[2,3] sigmatropic rearrangement of α-diazo-β-ketoesters po...
Rhodium-, copper- and iridium-catalyzed reactions of the <sup>13</sup>C-labelled diazo c...
Detailed in this account are our efforts toward efficient oxacycle syntheses. Two complementary appr...
We have developed catalyst-controlled regiodivergent rearrangements of onium-ylides derived from ind...
The synthesis and rearrangements of the chiral carbinols 8 and 9 are described. With KH-THF. both th...
Summary: Metal carbenes, divalent carbon species, are versatile intermediates that enable novel synt...
l,2-Dioxines are an important class of compounds that are useful in organic synthesis for the incorp...
Despite the importance of allylic ylide rearrangements for the synthesis of complex molecules, the c...
The first computational study of the rearrangement reactions of oxiranes initiated by lithium dialky...
Synthetically useful α,β-unsaturated carbonyl compounds were obtained from gold-catalyzed oxidative ...