The zwitterion formed by the reaction of dimethoxycarbene and DMAD adds efficiently to one of the carbonyl groups of 1,2-dicarbonyl compounds and anhydrides to generate dihydrofurans and spirodihydrofurans in good yields. In many cases, the carbene inserts into the C-C bond of the dione to yield masked vicinal tricarbonyl systems
352-356Oxidative addition of 1,3-dicarbonyl compounds to dienes constitutes a facile method for the...
This dissertation details the development and investigation of three independent research projects. ...
A new method was developed to synthesize polyfunctionalized dihydrofuran and tetrahydrofuran derivat...
The reaction of 1:1 zwitterionic species, generated in situ by the addition of dimethoxycarbene to d...
The vicinal tricarbonyl system participates in a novel reaction with the zwitterion derived from iso...
The Rh(II)-catalyzed reaction of dimethyl diazomalonate with aryl aldehydes and β-nitrostyrenes resu...
This paper describes the intermolecular generation of carbonyl ylides by dirhodium(II) tetraacetate-...
This paper describes the intermolecular generation of carbonyl ylides by dirhodium(II) tetraacetate-...
Carbon-carbon and carbon-heteroatom bond formations constitute the central events in organic synthes...
Polysubstituted tetrahydrofurans appear in a large variety of bioactive structures of both natural a...
Successful trapping of the carbonyl ylides generated from dicarbomethoxycarbene and aldehydes with 1...
The insertion reaction of alkylidene carbenes is demonstrated to be an effective method for the synt...
The insertion of vinylidene carbenes into C-H bonds is an efficient method for the synthesis of 2,5-...
The reaction of 1:1 zwitterionic intermediate generated in situ from dimethyl acetylenedicarboxylate...
An efficient and highly diastereoselective synthesis of highly substituted tetrahydrofurans from the...
352-356Oxidative addition of 1,3-dicarbonyl compounds to dienes constitutes a facile method for the...
This dissertation details the development and investigation of three independent research projects. ...
A new method was developed to synthesize polyfunctionalized dihydrofuran and tetrahydrofuran derivat...
The reaction of 1:1 zwitterionic species, generated in situ by the addition of dimethoxycarbene to d...
The vicinal tricarbonyl system participates in a novel reaction with the zwitterion derived from iso...
The Rh(II)-catalyzed reaction of dimethyl diazomalonate with aryl aldehydes and β-nitrostyrenes resu...
This paper describes the intermolecular generation of carbonyl ylides by dirhodium(II) tetraacetate-...
This paper describes the intermolecular generation of carbonyl ylides by dirhodium(II) tetraacetate-...
Carbon-carbon and carbon-heteroatom bond formations constitute the central events in organic synthes...
Polysubstituted tetrahydrofurans appear in a large variety of bioactive structures of both natural a...
Successful trapping of the carbonyl ylides generated from dicarbomethoxycarbene and aldehydes with 1...
The insertion reaction of alkylidene carbenes is demonstrated to be an effective method for the synt...
The insertion of vinylidene carbenes into C-H bonds is an efficient method for the synthesis of 2,5-...
The reaction of 1:1 zwitterionic intermediate generated in situ from dimethyl acetylenedicarboxylate...
An efficient and highly diastereoselective synthesis of highly substituted tetrahydrofurans from the...
352-356Oxidative addition of 1,3-dicarbonyl compounds to dienes constitutes a facile method for the...
This dissertation details the development and investigation of three independent research projects. ...
A new method was developed to synthesize polyfunctionalized dihydrofuran and tetrahydrofuran derivat...