Indexed keywords
1,2,3,4 TETRAHYDRO 1,6 DIMETHYL 2 OXOPHENYLPYRIMIDINE 5 CARBOXYLIC ACID;
1,2,3,4 TETRAHYDRO 1,6 DIMETHYL 4 (3 NITROPHENYL) 2 OXOPYRIMIDINE 5 CARBOXYLIC ACID;
1,2,3,4 TETRAHYDRO 6 METHYL 2 OXOPHENYLPYRIMIDINE 5 CARBOXYLIC ACID;
3 FLUOROBENZYL 6 METHYL 4 PHENYL 2 OXO 1,2,3,4 TETRAHYDROPYRIMIDINE 5 CARBOXYLATE;
ALLYL 1,6 DIMETHYL 4 (3 NITROPHENYL) 2 OXO 1,2,3,4 TETRAHYDROPYRIMIDINE 5 CARBOXYLATE;
ALLYL 6 METHYL 4 (2 CHLOROPHENYL) 2 THIOXO 1,2,3,4 TETRAHYDROPYRIMIDINE 5 CARBOXYLATE;
ALLYL 6 METHYL 4 (3 NITROPHENYL) 2 THIOXO 1,2,3,4 TETRAHYDROPYRIMIDINE 5 CARBOXYLATE;
ALLYL 6 METHYL 4 (4 BROMOPHENYL) 2 OXO 1,2,3,4 TETRAHYDROPYRIMIDINE 5 CARBOXYLATE;
ALLYL 6 METHYL 4 (4 CHLOROPHENYL) 2 OXO 1,2,3,4 TETRAHYDROPYRIMIDINE 5 CARBOXYLATE;
ALLYL 6 METHYL 4 PHENYL 2 THIOXO 1,2,3,4 TETRAHYDROPYRIMIDINE 5 CARBOXYLATE;
ALLYL 6 METHYL 4 TOLYL 2 THIOXO 1,2,3,4 TETRAHYDROPYRIMIDINE 5 CARBOXYLATE;
BENZYL 1,6 DIMETHYL 4 PHENYL 2 OXO 1,2,3,4 TETRAHYDROPYRIMIDINE 5 CARBOXYLATE;
BENZYL 4,6 DIPHENYL 2 OXO 1,2,3,4 TETRAHYDROPYRIMIDINE 5 CARBOXYLATE;
BENZYL 6 METHYL 4 PHENYL 2 OXO 1,2,3,4 TETRAHYDROPYRIMIDINE 5 CARBOXYLATE;
BENZYL 6 METHYL 4 TOLYL 2 OXO 1,2,3,4 TETRAHYDROPYRIMIDINE 5 CARBOXYLATE;
BUTYL 6 METHYL 4 PHENYL 2 OXO 1,2,3,4 TETRAHYDROPYRIMIDINE 5 CARBOXYLATE;
N BENZYL 1,2,3,4 TETRAHYDRO 1,6 DIMETHYL 2 OXO 4 (3 NITROPHENYL)PYRIMIDINE 5 CARBOXAMIDE;
N BENZYL 1,2,3,4 TETRAHYDRO 2 OXO 4,6 DIPHENYLPYRIMIDINE 5 CARBOXAMIDE;
N BENZYL 1,2,3,4 TETRAHYDRO 6 METHYL 2 OXO 4 (4 TOLYL)PYRIMIDINE 5 CARBOXAMIDE;
N BENZYL 1,2,3,4 TETRAHYDRO 6 METHYL 2 OXO 4 PHENYLPYRIMIDINE 5 CARBOXAMIDE;
N BENZYL 1,2,3,4 TETRAHYDRO 6 METHYL 2 THIOXO 4 (2 CHLOROPHENYL)PYRIMIDINE 5 CARBOXAMIDE;
N BENZYL 1,2,3,4 TETRAHYDRO 6 METHYL 2 THIOXO 4 (4 TOLYL)PYRIMIDINE 5 CARBOXAMIDE;
N PROPYL 1,2,3,4 TETRAHYDRO 1,6 DIMETHYL 2 OXO 4 PHENYLPYRIMIDINE 5 CARBOXAMIDE;
N PROPYL 1,2,3,4 TETRAHYDRO 6 METHYL 2 OXO 4 (4 BROMOPHENYL)PYRIMIDINE 5 CARBOXAMIDE;
N PROPYL 1,2,3,4 TETRAHYDRO 6 METHYL 2 THIOXO 4 (3 NITROPHENYL)PYRIMIDINE 5 CARBOXAMIDE;
N PROPYL 1,2,3,4 TETRAHYDRO 6 METHYL 2 THIOXO 4 PHENYLPYRIMIDINE 5 CARBOXAMIDE;
PROPYL 1 METHYL 6 METHYL 4 PHENYL 2 OXO 1,2,3,4 TETRAHYDROPYRIMIDINE 5 CARBOXYLATE;
PYRIMIDINE DERIVATIVE;
UNCLASSIFIED DRUG;
ARTICLE;
AUTOMATION;
BIGINELLI REACTION;
DEPROTECTION REACTION;
DRUG PURIFICATION;
DRUG STRUCTURE;
DRUG SYNTHESIS;
HYDROGENATION;
MICROWAVE RADIATION;
MITSUNOBU REACTION;
PRIORITY JOURNAL;
1
33645972149
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In addition, a solid-phase organic synthesis protocol to introduce carboxamido acid functionality on the C5 position of the DHPMs using amino acids as precursors was also reported:
In addition, a solid-phase organic synthesis protocol to introduce carboxamido acid functionality on the C5 position of the DHPMs using amino acids as precursors was also reported:. Zhang L., and Rana T.M. J. Comb. Chem. 6 (2004) 457
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note
In a collaboration with D. Sauer (Abbott Labs, USA) a library of 480 DHPM C5 amides of type 6 was generated by decorating the 10 DHPM acid cores 5a-j each with a set of 48 diverse amines. The procedure was performed in a fully robotic microwave synthesis station capable of automated reagent dispensing, vial handling and SPE purification.
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33646006909
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69
33645992647
For reviews on fluorous synthesis, see:
73
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Basic ion exchange Amberlite IRA-900 resin in carbonate form was prepared from Amberlite IRA-900 Cl ion exchange resin according to (preparation of Amberlyst A26 in bicarbonate form):
Basic ion exchange Amberlite IRA-900 resin in carbonate form was prepared from Amberlite IRA-900 Cl ion exchange resin according to (preparation of Amberlyst A26 in bicarbonate form):. Hodge P., Ji-Long J., Owen G.J., and Houghton M. Polymer 37 (1996) 5059
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