The Experts below are selected from a list of 1098 Experts worldwide ranked by ideXlab platform
Yanguang Wang - One of the best experts on this subject based on the ideXlab platform.
-
one pot three component synthesis of highly functionalized pyrimidone derivatives and access to indole fused pyrimidones via palladium catalyzed intramolecular heck reaction
ChemInform, 2014Co-Authors: Wan Tian, Ping Lu, Wei Li, Yanguang WangAbstract:A facile method for the synthesis of highly functionalized pyrimidone derivatives via three-component 1,4-dipolar cycloaddition is developed.
-
one pot three component synthesis of highly functionalized pyrimidone derivatives and access to indole fused pyrimidones via palladium catalyzed intramolecular heck reaction
Tetrahedron, 2014Co-Authors: Wan Tian, Ping Lu, Wei Li, Yanguang WangAbstract:Abstract A simple and facile approach to highly functionalized pyrimidone derivatives and indole fused pyrimidones has been developed. The synthesis of substituted pyrimidone derivatives in moderate to good yields involves [4+2] cycloaddition of 1,4-dipoles generated from α,β-unsarurated imines and dimethyl acetylenedicarboxylate (DMAD) with isocyanates as dipolarophiles. Furthermore, the pyrimidones resulted from 2-bromophenyl isocyanate could be transformed into various indole fused pyrimidones via intramolecular palladium-catalyzed Heck reaction under different conditions.
Wan Tian - One of the best experts on this subject based on the ideXlab platform.
-
one pot three component synthesis of highly functionalized pyrimidone derivatives and access to indole fused pyrimidones via palladium catalyzed intramolecular heck reaction
ChemInform, 2014Co-Authors: Wan Tian, Ping Lu, Wei Li, Yanguang WangAbstract:A facile method for the synthesis of highly functionalized pyrimidone derivatives via three-component 1,4-dipolar cycloaddition is developed.
-
one pot three component synthesis of highly functionalized pyrimidone derivatives and access to indole fused pyrimidones via palladium catalyzed intramolecular heck reaction
Tetrahedron, 2014Co-Authors: Wan Tian, Ping Lu, Wei Li, Yanguang WangAbstract:Abstract A simple and facile approach to highly functionalized pyrimidone derivatives and indole fused pyrimidones has been developed. The synthesis of substituted pyrimidone derivatives in moderate to good yields involves [4+2] cycloaddition of 1,4-dipoles generated from α,β-unsarurated imines and dimethyl acetylenedicarboxylate (DMAD) with isocyanates as dipolarophiles. Furthermore, the pyrimidones resulted from 2-bromophenyl isocyanate could be transformed into various indole fused pyrimidones via intramolecular palladium-catalyzed Heck reaction under different conditions.
Ping Lu - One of the best experts on this subject based on the ideXlab platform.
-
one pot three component synthesis of highly functionalized pyrimidone derivatives and access to indole fused pyrimidones via palladium catalyzed intramolecular heck reaction
ChemInform, 2014Co-Authors: Wan Tian, Ping Lu, Wei Li, Yanguang WangAbstract:A facile method for the synthesis of highly functionalized pyrimidone derivatives via three-component 1,4-dipolar cycloaddition is developed.
-
one pot three component synthesis of highly functionalized pyrimidone derivatives and access to indole fused pyrimidones via palladium catalyzed intramolecular heck reaction
Tetrahedron, 2014Co-Authors: Wan Tian, Ping Lu, Wei Li, Yanguang WangAbstract:Abstract A simple and facile approach to highly functionalized pyrimidone derivatives and indole fused pyrimidones has been developed. The synthesis of substituted pyrimidone derivatives in moderate to good yields involves [4+2] cycloaddition of 1,4-dipoles generated from α,β-unsarurated imines and dimethyl acetylenedicarboxylate (DMAD) with isocyanates as dipolarophiles. Furthermore, the pyrimidones resulted from 2-bromophenyl isocyanate could be transformed into various indole fused pyrimidones via intramolecular palladium-catalyzed Heck reaction under different conditions.
Wei Li - One of the best experts on this subject based on the ideXlab platform.
-
one pot three component synthesis of highly functionalized pyrimidone derivatives and access to indole fused pyrimidones via palladium catalyzed intramolecular heck reaction
ChemInform, 2014Co-Authors: Wan Tian, Ping Lu, Wei Li, Yanguang WangAbstract:A facile method for the synthesis of highly functionalized pyrimidone derivatives via three-component 1,4-dipolar cycloaddition is developed.
-
one pot three component synthesis of highly functionalized pyrimidone derivatives and access to indole fused pyrimidones via palladium catalyzed intramolecular heck reaction
Tetrahedron, 2014Co-Authors: Wan Tian, Ping Lu, Wei Li, Yanguang WangAbstract:Abstract A simple and facile approach to highly functionalized pyrimidone derivatives and indole fused pyrimidones has been developed. The synthesis of substituted pyrimidone derivatives in moderate to good yields involves [4+2] cycloaddition of 1,4-dipoles generated from α,β-unsarurated imines and dimethyl acetylenedicarboxylate (DMAD) with isocyanates as dipolarophiles. Furthermore, the pyrimidones resulted from 2-bromophenyl isocyanate could be transformed into various indole fused pyrimidones via intramolecular palladium-catalyzed Heck reaction under different conditions.
Rajagopal Nagarajan - One of the best experts on this subject based on the ideXlab platform.
-
nis mediated regioselective amidation of indole with quinazolinone and pyrimidone
ChemInform, 2015Co-Authors: Suman Kr Ghosh, Rajagopal NagarajanAbstract:A direct regioselective C2 amidation of pyrroles and indoles with pyrimidone and quinazolinone derivatives is developed.
-
nis mediated regioselective amidation of indole with quinazolinone and pyrimidone
RSC Advances, 2014Co-Authors: Suman Kr Ghosh, Rajagopal NagarajanAbstract:A mild, metal-free condition was developed for the direct regioselective C2 amidation of indoles and pyrroles with quinazolinone and pyrimidone derivatives in intermolecular fashion, which led to novel indolyl/pyrrolyl quinazolinone and pyrimidone derivatives in moderate to good yields.