Intermolecular Diels-Alder reaction of the diene I, formed in the thermal decarbonylation of the keto-anhydride II in the presence of maleic anhydride, followed by esterification generates the title compound III
5-(1-Menthyloxy)-2(5H)-furanone was used as a chiral dienophile in thermal asymmetric Diels-Alder re...
The title compound, C27H29NO11, is a product of the tandem domino Diels-Alder reaction. The mol-ecul...
The title compound, C27H29NO11, is a product of the tandem `domino' Diels–Alder reaction. ...
Intermolecular Diels-Alder reaction of the diene I, formed in the thermal decarbonylation of the ket...
Endo cis-4-cyclohexane-1,2-dicarboxylic anhydride Synthesis through Diels-Alder Three common reactio...
An economical route to the title system, starting from COT-MA Diels-Alder adduct 2 via the ketoanhyd...
Synthesis of methyl 2, 7-dimethyltricyclo{5.2.2.0(1,5}undec-5-en-6-carboxylates, the tricyclic skele...
The structure of the by-product, obtained in the Diels-Alder condensation of maleic anhydride with β...
The structure of the by-product, obtained in the Diels-Alder condensation of maleic anhydride with β...
Synthesis of methyl 2, 7-dimethyltricyclo{5.2.2.0(1,5}undec-5-en-6-carboxylates, the tricyclic skele...
5-(1-Menthyloxy)-2(5H)-furanone was used as a chiral dienophile in thermal asymmetric Diels-Alder re...
5-(1-Menthyloxy)-2(5H)-furanone was used as a chiral dienophile in thermal asymmetric Diels-Alder re...
5-(1-Menthyloxy)-2(5H)-furanone was used as a chiral dienophile in thermal asymmetric Diels-Alder re...
The title compound, C27H29NO11, is a product of the tandem domino Diels-Alder reaction. The mol-ecul...
The title compound, C26H36O5, is a derivative of abietic acid formed by an endo-Diels-Alder reaction...
5-(1-Menthyloxy)-2(5H)-furanone was used as a chiral dienophile in thermal asymmetric Diels-Alder re...
The title compound, C27H29NO11, is a product of the tandem domino Diels-Alder reaction. The mol-ecul...
The title compound, C27H29NO11, is a product of the tandem `domino' Diels–Alder reaction. ...
Intermolecular Diels-Alder reaction of the diene I, formed in the thermal decarbonylation of the ket...
Endo cis-4-cyclohexane-1,2-dicarboxylic anhydride Synthesis through Diels-Alder Three common reactio...
An economical route to the title system, starting from COT-MA Diels-Alder adduct 2 via the ketoanhyd...
Synthesis of methyl 2, 7-dimethyltricyclo{5.2.2.0(1,5}undec-5-en-6-carboxylates, the tricyclic skele...
The structure of the by-product, obtained in the Diels-Alder condensation of maleic anhydride with β...
The structure of the by-product, obtained in the Diels-Alder condensation of maleic anhydride with β...
Synthesis of methyl 2, 7-dimethyltricyclo{5.2.2.0(1,5}undec-5-en-6-carboxylates, the tricyclic skele...
5-(1-Menthyloxy)-2(5H)-furanone was used as a chiral dienophile in thermal asymmetric Diels-Alder re...
5-(1-Menthyloxy)-2(5H)-furanone was used as a chiral dienophile in thermal asymmetric Diels-Alder re...
5-(1-Menthyloxy)-2(5H)-furanone was used as a chiral dienophile in thermal asymmetric Diels-Alder re...
The title compound, C27H29NO11, is a product of the tandem domino Diels-Alder reaction. The mol-ecul...
The title compound, C26H36O5, is a derivative of abietic acid formed by an endo-Diels-Alder reaction...
5-(1-Menthyloxy)-2(5H)-furanone was used as a chiral dienophile in thermal asymmetric Diels-Alder re...
The title compound, C27H29NO11, is a product of the tandem domino Diels-Alder reaction. The mol-ecul...
The title compound, C27H29NO11, is a product of the tandem `domino' Diels–Alder reaction. ...