Heterogeneous hydrogenation reactions using a continuous flow high pressure device

[21] Multiphase catalytic reactor engineering and design for pharmaceuticals and fine chemicals [J]. CATALYSIS TODAY, 1997, 37 (04) : 367 - 404

[22] Nishimura S., 2001, Handbook of Heterogeneous Catalytic Hydrogenation for Organic Synthesis

[23] Rylander P. N., 1979, Catalytic Hydrogenation in Organic Syntheses

[24] The use of a continuous flow-reactor employing a mixed hydrogen-liquid flow stream for the efficient reduction of imines to amines [J]. CHEMICAL COMMUNICATIONS, 2005, (23) : 2909 - 2911

[25] Microwave-assisted synthesis utilizing supported reagents: A rapid and efficient acylation procedure [J]. ORGANIC LETTERS, 2003, 5 (24) : 4721 - 4724

[26] Synthesis and reactions of Biginelli-compounds.: Part 23.: Chemoenzymatic syntheses of enantiomerically pure 4-aryl-3,4-dihydropyrimidin-2(1H)-ones [J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 2000, (24): : 4382 - 4389

[27] Spadoni C, 2005, CHIM OGGI, V23, P36

[28] Expedient synthesis of 5-unsubstituted 3,4-dihydropyrimidin-2(1H)-ones. [J]. TETRAHEDRON LETTERS, 1998, 39 (51) : 9315 - 9318

[29] A tandem intramolecular Michael-addition/elimination sequence in dihydropyrimidone to quinoline rearrangements [J]. ARKIVOC, 2002, : 71 - 79

[30] Tundo P., 1991, CONTINUOUS FLOW METH

[21] Multiphase catalytic reactor engineering and design for pharmaceuticals and fine chemicals [J]. CATALYSIS TODAY, 1997, 37 (04) : 367 - 404

[22] Nishimura S., 2001, Handbook of Heterogeneous Catalytic Hydrogenation for Organic Synthesis

[23] Rylander P. N., 1979, Catalytic Hydrogenation in Organic Syntheses

[24] The use of a continuous flow-reactor employing a mixed hydrogen-liquid flow stream for the efficient reduction of imines to amines [J]. CHEMICAL COMMUNICATIONS, 2005, (23) : 2909 - 2911

[25] Microwave-assisted synthesis utilizing supported reagents: A rapid and efficient acylation procedure [J]. ORGANIC LETTERS, 2003, 5 (24) : 4721 - 4724

[26] Synthesis and reactions of Biginelli-compounds.: Part 23.: Chemoenzymatic syntheses of enantiomerically pure 4-aryl-3,4-dihydropyrimidin-2(1H)-ones [J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 2000, (24): : 4382 - 4389

[27] Spadoni C, 2005, CHIM OGGI, V23, P36

[28] Expedient synthesis of 5-unsubstituted 3,4-dihydropyrimidin-2(1H)-ones. [J]. TETRAHEDRON LETTERS, 1998, 39 (51) : 9315 - 9318

[29] A tandem intramolecular Michael-addition/elimination sequence in dihydropyrimidone to quinoline rearrangements [J]. ARKIVOC, 2002, : 71 - 79

[30] Tundo P., 1991, CONTINUOUS FLOW METH