The use of bulky Lewis acids, aluminum tris(2,6-diphenylphenoxide) (ATPH) and aluminum tris(2,6-di-2-naphthylphenoxide) (ATNP), in the doubly vinylogous aldol reaction between methyl-5-methyl-2-furoate and aldehydes or ketones is described. These reactions proceed smoothly and in high yields with both enolizable and non-enolizable substrates. This C–C bond-forming reaction enables a new bond construction for the synthesis of functionalized furans
Two carbon homologation of aromatic and heterocyclic aldehydes is achieved by reacting them with ace...
In this paper the aldol condensation of furfural (C5) with acetone (C3) over Ca/ZSM-5 was studied wi...
Formaldehyde is used as a one-carbon electrophile(1) in several organic transformations to functiona...
The synthesis of the novel Lewis acid, aluminum tris(2,6-di-2-naphthylphenoxide) (ATNP), and its use...
textAldol reactions are widely used in forming new carbon-carbon bonds. Since the discovery of the a...
The vinylogous aldol reactions provides access to a range of structurally diverse targets but has lo...
Metallated difluoroenol carbamate 1 reacted with aldehydes and ketones in the presence of highly oxo...
Vicinally substituted trimethylsilylmethyl cyclopropyl ketones undergo facile desilylative ring open...
NaOH catalyzed condensation reaction between 5-hydroxymethylfurfural and levulinic acid in water giv...
Alditols have been obtained in very high yield using an excess of electron-rich furans with respect ...
M.Sc.The objective of the project described in this dissertation was to develop environmentally beni...
A vinylogous, silylative, and direct variant of the venerable Mukaiyama aldol reaction has been deve...
Silica sulfuric acid was found to be an efficient catalyst for the vinylogous Mukaiyama aldol reacti...
A Lewis base-catalyzed intramolecular vinylogous aldol reaction of o-(allyloxy)phenyl ketoesters or ...
International audienceA one-pot synthesis of 2,5-disubstituted furans from γ-ketoacids is reported. ...
Two carbon homologation of aromatic and heterocyclic aldehydes is achieved by reacting them with ace...
In this paper the aldol condensation of furfural (C5) with acetone (C3) over Ca/ZSM-5 was studied wi...
Formaldehyde is used as a one-carbon electrophile(1) in several organic transformations to functiona...
The synthesis of the novel Lewis acid, aluminum tris(2,6-di-2-naphthylphenoxide) (ATNP), and its use...
textAldol reactions are widely used in forming new carbon-carbon bonds. Since the discovery of the a...
The vinylogous aldol reactions provides access to a range of structurally diverse targets but has lo...
Metallated difluoroenol carbamate 1 reacted with aldehydes and ketones in the presence of highly oxo...
Vicinally substituted trimethylsilylmethyl cyclopropyl ketones undergo facile desilylative ring open...
NaOH catalyzed condensation reaction between 5-hydroxymethylfurfural and levulinic acid in water giv...
Alditols have been obtained in very high yield using an excess of electron-rich furans with respect ...
M.Sc.The objective of the project described in this dissertation was to develop environmentally beni...
A vinylogous, silylative, and direct variant of the venerable Mukaiyama aldol reaction has been deve...
Silica sulfuric acid was found to be an efficient catalyst for the vinylogous Mukaiyama aldol reacti...
A Lewis base-catalyzed intramolecular vinylogous aldol reaction of o-(allyloxy)phenyl ketoesters or ...
International audienceA one-pot synthesis of 2,5-disubstituted furans from γ-ketoacids is reported. ...
Two carbon homologation of aromatic and heterocyclic aldehydes is achieved by reacting them with ace...
In this paper the aldol condensation of furfural (C5) with acetone (C3) over Ca/ZSM-5 was studied wi...
Formaldehyde is used as a one-carbon electrophile(1) in several organic transformations to functiona...