The Experts below are selected from a list of 6180 Experts worldwide ranked by ideXlab platform
Gunter Haufe - One of the best experts on this subject based on the ideXlab platform.
-
diels alder reaction of ethyl 3 benzamido 2 oxo 6 trifluoromethyl 2h pyran 5 carboxylate with alkoxyalkenes as an effective approach to trifluoromethyl containing 3 Aminobenzoic Acid derivatives
ChemInform, 2015Co-Authors: Ivan S Kondratov, Nataliya A Tolmachova, Violetta G Dolovanyuk, Igor I Gerus, Klaus Bergander, Constantingabriel Daniliuc, Gunter HaufeAbstract:Diels—Alder reaction of pyrone (I) with alkoxy alkenes at 120 °C provides the corresponding cycloadducts (III) and (IV).
-
diels alder reaction of ethyl 3 benzamido 2 oxo 6 trifluoromethyl 2h pyran 5 carboxylate with alkoxyalkenes as an effective approach to trifluoromethyl containing 3 Aminobenzoic Acid derivatives
European Journal of Organic Chemistry, 2014Co-Authors: Ivan S Kondratov, Nataliya A Tolmachova, Violetta G Dolovanyuk, Igor I Gerus, Klaus Bergander, Constantingabriel Daniliuc, Gunter HaufeAbstract:The Diels–Alder reactions of ethyl 3-benzamido-2-oxo-6-(trifluoromethyl)-2H-pyran-5-carboxylate with ethyl vinyl ether, 2-methoxypropene, and 1-ethoxypropene were investigated. Under different reaction conditions, intermediate oxabicyclo[2.2.2]octenones, alkoxycyclohexadienes, or aromatic products [5-benzamido-2-(trifluoromethyl)benzoates] were formed. The reaction is useful for the preparation of some hitherto unknown trifluoromethyl-containing derivatives of 3-Aminobenzoic Acid.
Ivan S Kondratov - One of the best experts on this subject based on the ideXlab platform.
-
diels alder reaction of ethyl 3 benzamido 2 oxo 6 trifluoromethyl 2h pyran 5 carboxylate with alkoxyalkenes as an effective approach to trifluoromethyl containing 3 Aminobenzoic Acid derivatives
ChemInform, 2015Co-Authors: Ivan S Kondratov, Nataliya A Tolmachova, Violetta G Dolovanyuk, Igor I Gerus, Klaus Bergander, Constantingabriel Daniliuc, Gunter HaufeAbstract:Diels—Alder reaction of pyrone (I) with alkoxy alkenes at 120 °C provides the corresponding cycloadducts (III) and (IV).
-
diels alder reaction of ethyl 3 benzamido 2 oxo 6 trifluoromethyl 2h pyran 5 carboxylate with alkoxyalkenes as an effective approach to trifluoromethyl containing 3 Aminobenzoic Acid derivatives
European Journal of Organic Chemistry, 2014Co-Authors: Ivan S Kondratov, Nataliya A Tolmachova, Violetta G Dolovanyuk, Igor I Gerus, Klaus Bergander, Constantingabriel Daniliuc, Gunter HaufeAbstract:The Diels–Alder reactions of ethyl 3-benzamido-2-oxo-6-(trifluoromethyl)-2H-pyran-5-carboxylate with ethyl vinyl ether, 2-methoxypropene, and 1-ethoxypropene were investigated. Under different reaction conditions, intermediate oxabicyclo[2.2.2]octenones, alkoxycyclohexadienes, or aromatic products [5-benzamido-2-(trifluoromethyl)benzoates] were formed. The reaction is useful for the preparation of some hitherto unknown trifluoromethyl-containing derivatives of 3-Aminobenzoic Acid.
Nataliya A Tolmachova - One of the best experts on this subject based on the ideXlab platform.
-
diels alder reaction of ethyl 3 benzamido 2 oxo 6 trifluoromethyl 2h pyran 5 carboxylate with alkoxyalkenes as an effective approach to trifluoromethyl containing 3 Aminobenzoic Acid derivatives
ChemInform, 2015Co-Authors: Ivan S Kondratov, Nataliya A Tolmachova, Violetta G Dolovanyuk, Igor I Gerus, Klaus Bergander, Constantingabriel Daniliuc, Gunter HaufeAbstract:Diels—Alder reaction of pyrone (I) with alkoxy alkenes at 120 °C provides the corresponding cycloadducts (III) and (IV).
-
diels alder reaction of ethyl 3 benzamido 2 oxo 6 trifluoromethyl 2h pyran 5 carboxylate with alkoxyalkenes as an effective approach to trifluoromethyl containing 3 Aminobenzoic Acid derivatives
European Journal of Organic Chemistry, 2014Co-Authors: Ivan S Kondratov, Nataliya A Tolmachova, Violetta G Dolovanyuk, Igor I Gerus, Klaus Bergander, Constantingabriel Daniliuc, Gunter HaufeAbstract:The Diels–Alder reactions of ethyl 3-benzamido-2-oxo-6-(trifluoromethyl)-2H-pyran-5-carboxylate with ethyl vinyl ether, 2-methoxypropene, and 1-ethoxypropene were investigated. Under different reaction conditions, intermediate oxabicyclo[2.2.2]octenones, alkoxycyclohexadienes, or aromatic products [5-benzamido-2-(trifluoromethyl)benzoates] were formed. The reaction is useful for the preparation of some hitherto unknown trifluoromethyl-containing derivatives of 3-Aminobenzoic Acid.
Violetta G Dolovanyuk - One of the best experts on this subject based on the ideXlab platform.
-
diels alder reaction of ethyl 3 benzamido 2 oxo 6 trifluoromethyl 2h pyran 5 carboxylate with alkoxyalkenes as an effective approach to trifluoromethyl containing 3 Aminobenzoic Acid derivatives
ChemInform, 2015Co-Authors: Ivan S Kondratov, Nataliya A Tolmachova, Violetta G Dolovanyuk, Igor I Gerus, Klaus Bergander, Constantingabriel Daniliuc, Gunter HaufeAbstract:Diels—Alder reaction of pyrone (I) with alkoxy alkenes at 120 °C provides the corresponding cycloadducts (III) and (IV).
-
diels alder reaction of ethyl 3 benzamido 2 oxo 6 trifluoromethyl 2h pyran 5 carboxylate with alkoxyalkenes as an effective approach to trifluoromethyl containing 3 Aminobenzoic Acid derivatives
European Journal of Organic Chemistry, 2014Co-Authors: Ivan S Kondratov, Nataliya A Tolmachova, Violetta G Dolovanyuk, Igor I Gerus, Klaus Bergander, Constantingabriel Daniliuc, Gunter HaufeAbstract:The Diels–Alder reactions of ethyl 3-benzamido-2-oxo-6-(trifluoromethyl)-2H-pyran-5-carboxylate with ethyl vinyl ether, 2-methoxypropene, and 1-ethoxypropene were investigated. Under different reaction conditions, intermediate oxabicyclo[2.2.2]octenones, alkoxycyclohexadienes, or aromatic products [5-benzamido-2-(trifluoromethyl)benzoates] were formed. The reaction is useful for the preparation of some hitherto unknown trifluoromethyl-containing derivatives of 3-Aminobenzoic Acid.
Igor I Gerus - One of the best experts on this subject based on the ideXlab platform.
-
diels alder reaction of ethyl 3 benzamido 2 oxo 6 trifluoromethyl 2h pyran 5 carboxylate with alkoxyalkenes as an effective approach to trifluoromethyl containing 3 Aminobenzoic Acid derivatives
ChemInform, 2015Co-Authors: Ivan S Kondratov, Nataliya A Tolmachova, Violetta G Dolovanyuk, Igor I Gerus, Klaus Bergander, Constantingabriel Daniliuc, Gunter HaufeAbstract:Diels—Alder reaction of pyrone (I) with alkoxy alkenes at 120 °C provides the corresponding cycloadducts (III) and (IV).
-
diels alder reaction of ethyl 3 benzamido 2 oxo 6 trifluoromethyl 2h pyran 5 carboxylate with alkoxyalkenes as an effective approach to trifluoromethyl containing 3 Aminobenzoic Acid derivatives
European Journal of Organic Chemistry, 2014Co-Authors: Ivan S Kondratov, Nataliya A Tolmachova, Violetta G Dolovanyuk, Igor I Gerus, Klaus Bergander, Constantingabriel Daniliuc, Gunter HaufeAbstract:The Diels–Alder reactions of ethyl 3-benzamido-2-oxo-6-(trifluoromethyl)-2H-pyran-5-carboxylate with ethyl vinyl ether, 2-methoxypropene, and 1-ethoxypropene were investigated. Under different reaction conditions, intermediate oxabicyclo[2.2.2]octenones, alkoxycyclohexadienes, or aromatic products [5-benzamido-2-(trifluoromethyl)benzoates] were formed. The reaction is useful for the preparation of some hitherto unknown trifluoromethyl-containing derivatives of 3-Aminobenzoic Acid.