-
1
-
-
0000884192
-
Solvent free organic synthesis
-
Tanaka, K.; Toda, F. Solvent free organic synthesis. Chem. Rev. 2000, 100, 1025.
-
(2000)
Chem. Rev.
, vol.100
, pp. 1025
-
-
Tanaka, K.1
Toda, F.2
-
2
-
-
0024818583
-
Substituted 1,4-dihydropyrimidines. 3. Synthesis of selectively functionalized 2-hetero 1,4-dihydropyrimidines
-
(a) Atwal, K.S.; Rovnyak, G.C.; O'Reilly, B.C.; Schwartz, J. Substituted 1,4-dihydropyrimidines. 3. Synthesis of selectively functionalized 2-hetero 1,4-dihydropyrimidines. J. Org. Chem. 1989, 54, 5898;
-
(1989)
J. Org. Chem.
, vol.54
, pp. 5898
-
-
Atwal, K.S.1
Rovnyak, G.C.2
O'Reilly, B.C.3
Schwartz, J.4
-
3
-
-
0029036894
-
Calcium entry blockers and activators: Conformational and structural determinants of dihydropyrimidine calcium channel modulators
-
(b) Rovnyak, G.C.; Kimball, S.D.; Beyer, B.; Cucinotta, G.; Dimarco, J.D.; Gougoutas, J.; Hedberg, A.; Malley, M.; McCarthy, J.P.; Zhang, R.; Moreland, S. Calcium entry blockers and activators: conformational and structural determinants of dihydropyrimidine calcium channel modulators. J. Med. Chem. 1995, 38, 119.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 119
-
-
Rovnyak, G.C.1
Kimball, S.D.2
Beyer, B.3
Cucinotta, G.4
Dimarco, J.D.5
Gougoutas, J.6
Hedberg, A.7
Malley, M.8
McCarthy, J.P.9
Zhang, R.10
Moreland, S.11
-
4
-
-
0031584880
-
Conformational analysis of 4-aryl-dihydropyrimidine calcium channel modulators. A comparison of Ab-initio, semiemperical, and x-ray crystallographic studies
-
(a) Kappe, C.O.; Fabian, W.M.F.; Semones, M.A. Conformational analysis of 4-aryl-dihydropyrimidine calcium channel modulators. A comparison of ab-initio, semiemperical, and x-ray crystallographic studies. Tetrahedron 1997, 53, 2803;
-
(1997)
Tetrahedron
, vol.53
, pp. 2803
-
-
Kappe, C.O.1
Fabian, W.M.F.2
Semones, M.A.3
-
5
-
-
0032524801
-
Unprecedented catalutic three component one-pot condensation reaction: An efficient synthesis of 5-alkoxycarbonyl-4-aryl-3,4-dihydropyrimidin-2(1H)-ones
-
(b) Hu, E.H.; Sidler, D.R.; Dolling, U.H. Unprecedented catalutic three component one-pot condensation reaction: an efficient synthesis of 5-alkoxycarbonyl-4-aryl-3,4-dihydropyrimidin-2(1H)-ones. J. Org. Chem. 1998, 63, 3454.
-
(1998)
J. Org. Chem.
, vol.63
, pp. 3454
-
-
Hu, E.H.1
Sidler, D.R.2
Dolling, U.H.3
-
6
-
-
0026065919
-
Dihydropyrimidine calcium channel blockers. 3,3-Carbamoyl-4-aryl-1,2,3,4-tetrahydro-6-methyl-5-pyrimidine carboxylic acid esters as orally efffective antihypertensive agents
-
Atwal, K.S.; Swanson, B.N.; Unger, S.E.; Floyd, D.M.; Moreland, S.; Hedberg, A.; O'Reilly, B.C. Dihydropyrimidine calcium channel blockers. 3,3-carbamoyl-4-aryl-1,2,3,4-tetrahydro-6-methyl-5-pyrimidine carboxylic acid esters as orally efffective antihypertensive agents. J. Med. Chem. 1991, 34, 806.
-
(1991)
J. Med. Chem.
, vol.34
, pp. 806
-
-
Atwal, K.S.1
Swanson, B.N.2
Unger, S.E.3
Floyd, D.M.4
Moreland, S.5
Hedberg, A.6
O'Reilly, B.C.7
-
7
-
-
0029095690
-
-
Grover, G.J.; Dzwonczyk, S.; McMullen, D.M.; Normadinam, C.S.; Sleph, P.G.; Moreland, S.J. J. Cardiovasc. Pharmacol. 1995, 26, 289.
-
(1995)
J. Cardiovasc. Pharmacol.
, vol.26
, pp. 289
-
-
Grover, G.J.1
Dzwonczyk, S.2
McMullen, D.M.3
Normadinam, C.S.4
Sleph, P.G.5
Moreland, S.J.6
-
8
-
-
0028939869
-
Enantioselective total synthesis of (-)-ptibmycalin A
-
(a) Overman, L.E.; Rabinowitz, M.H.; Renhowe, P.A. Enantioselective total synthesis of (-)-ptibmycalin A. J. Am. Chem. Soc. 1995, 117, 2657;
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 2657
-
-
Overman, L.E.1
Rabinowitz, M.H.2
Renhowe, P.A.3
-
9
-
-
33751385241
-
Biomimetic synthesis of (0 ± 0)-crambines A, B, C1, C2. Revision of the structure of crambines B and C1
-
(b) Snider, B.; Shi, Z. Biomimetic synthesis of (0 ± 0)-crambines A, B, C1, and C2. Revision of the structure of crambines B and C1. J. Org. Chem. 1993, 58, 3828.
-
(1993)
J. Org. Chem.
, vol.58
, pp. 3828
-
-
Snider, B.1
Shi, Z.2
-
10
-
-
0036759851
-
Samarium chloride catalyzed Biginelli reaction: One-pot synthesis of 3,4-dihydropyrimidin-2(1H)-ones
-
(a) Fan, X.; Zhang, X.; Zhang, Y. Samarium chloride catalyzed Biginelli reaction: one-pot synthesis of 3,4-dihydropyrimidin-2(1H)-ones. J. Chem. Res. (S) 2002, 436;
-
(2002)
J. Chem. Res. (S)
, pp. 436
-
-
Fan, X.1
Zhang, X.2
Zhang, Y.3
-
11
-
-
0036193521
-
Catalysis of the Biginelli reaction by ferric and nickel chloride hexahydrates. One-pot synthesis of 3,4-dihydropyridine-2-(1H)-ones
-
(b) Lu, J.; Bai, Y. Catalysis of the Biginelli reaction by ferric and nickel chloride hexahydrates. one-pot synthesis of 3,4-dihydropyridine-2-(1H)-ones. Synthesis 2002, 466;
-
(2002)
Synthesis.
, pp. 466
-
-
Lu, J.1
Bai, Y.2
-
12
-
-
0036125953
-
A simple and efficient synthesis of 3,4-dihydropyrimidin-2-ones catalyzed by amidosulfonic acid
-
(c) Jin, T.; Zhang, S.; Guo, J.; Li, T. A simple and efficient synthesis of 3,4-dihydropyrimidin-2-ones catalyzed by amidosulfonic acid. J. Chem. Res. (S) 2002, 37;
-
(2002)
J. Chem. Res. (S)
, pp. 37
-
-
Jin, T.1
Zhang, S.2
Guo, J.3
Li, T.4
-
13
-
-
0037244559
-
Bismuth triflate catalyzed one-pot synthesis of 3,4-dihydropyrimidin-2-(1H)-ones: An improved protocal for the Biginelli reaction
-
(d) Varala, R.; Alam, M.M.; Adapa, S.R. Bismuth triflate catalyzed one-pot synthesis of 3,4-dihydropyrimidin-2-(1H)-ones: an improved protocal for the Biginelli reaction. Synlett. 2003, 67;
-
(2003)
Synlett
, pp. 67
-
-
Varala, R.1
Alam, M.M.2
Adapa, S.R.3
-
14
-
-
0038632309
-
One-pot synthesis of dihydropyrimidinones using iodotrimethylsilane; facile and new improved protocal for the Biginelli reaction at room temperature
-
(e) Kiran Kumar Reddy, G.S.; Srinivas Reddy, Ch.; Yadav, J.S.; Sabitha, G. One-pot synthesis of dihydropyrimidinones using iodotrimethylsilane; facile and new improved protocal for the Biginelli reaction at room temperature. Synlett. 2003, 858;
-
(2003)
Synlett
, pp. 858
-
-
Kiran Kumar Reddy, G.S.1
Srinivas Reddy, Ch.2
Yadav, J.S.3
Sabitha, G.4
-
15
-
-
0034703416
-
Indium(III) chloride-catalyzed one-pot synthesis of dihydropyrimidinones by a three-component coupling of 1,3-dicarbonyl compounds, aldehydes and urea: An improved procedure for the Biginelli reaction
-
(f) Ranu, B.C.; Hajra, A.; Jana, U. Indium(III) chloride-catalyzed one-pot synthesis of dihydropyrimidinones by a three-component coupling of 1,3-dicarbonyl compounds, aldehydes, and urea: an improved procedure for the Biginelli reaction. J. Org. Chem. 2000, 65, 6270;
-
(2000)
J. Org. Chem.
, vol.65
, pp. 6270
-
-
Ranu, B.C.1
Hajra, A.2
Jana, U.3
-
16
-
-
0034674776
-
Lanthanide triflate catalyzed Biginelli reaction. One-pot synthesis of dihydropyrimidinone under solvent-free conditions
-
(g) Yun, M.; Changtao, Q.; Limin, W.; Min, Y. Lanthanide triflate catalyzed Biginelli reaction. One-pot synthesis of dihydropyrimidinone under solvent-free conditions. J. Org. Chem. 2000, 65, 3864;
-
(2000)
J. Org. Chem.
, vol.65
, pp. 3864
-
-
Yun, M.1
Changtao, Q.2
Limin, W.3
Min, Y.4
-
18
-
-
0037462396
-
Green chemistry approaches to the synthesis of 5-alkoxycarbonyl-4-aryl-3,4-dihydropyrimidin-2(1H)-ones by a three component coupling of one-pot condensation reaction: Comparison of ethanol, water, and solvent-free conditions
-
(i) Bose, D.S.; Fatima, L.; Mereyala, H.B. Green chemistry approaches to the synthesis of 5-alkoxycarbonyl-4-aryl-3,4-dihydropyrimidin-2(1H)-ones by a three component coupling of one-pot condensation reaction: comparison of ethanol, water, and solvent-free conditions. J. Org. Chem. 2003, 68, 587.
-
(2003)
J. Org. Chem.
, vol.68
, pp. 587
-
-
Bose, D.S.1
Fatima, L.2
Mereyala, H.B.3
-
20
-
-
0035851385
-
A facile and efficient method for the rearrangement of aryl-substituted epoxides to aldehydes and ketones using bismuth triflate
-
(b) Bhatia, K.A.; Eash, K.J.; Leonard; N.M.; Oswald, M.C.; Mohan, R.S. A facile and efficient method for the rearrangement of aryl-substituted epoxides to aldehydes and ketones using bismuth triflate. Tetrahedron Lett. 2001, 46, 8129;
-
(2001)
Tetrahedron Lett.
, vol.46
, pp. 8129
-
-
Bhatia, K.A.1
Eash, K.J.2
Leonard, N.M.3
Oswald, M.C.4
Mohan, R.S.5
-
21
-
-
0036166340
-
Bismuth(III) chloride and triflate: Novel catalysts for acylation and sulfonylation reactions. Survey and mechanistic aspects
-
(c) Roux, C.L.; Dubac, J. Bismuth(III) chloride and triflate: novel catalysts for acylation and sulfonylation reactions. Survey and mechanistic aspects. Synlett. 2002, 2, 181.
-
(2002)
Synlett
, vol.2
, pp. 181
-
-
Roux, C.L.1
Dubac, J.2
-
22
-
-
57249111561
-
Efficient and selective conversion of trimethylsilyl and tetrahydropyranyl ethers to their corresponding acetates and benzoates catalyzed by bismuth(III) salts
-
(a) Mohammadpoor-Baltork, I.; Khosropour, A.R. Efficient and selective conversion of trimethylsilyl and tetrahydropyranyl ethers to their corresponding acetates and benzoates catalyzed by bismuth(III) salts. Monatshefte für Chemie 2002, 133, 189;
-
(2002)
Monatshefte für Chemie
, vol.133
, pp. 189
-
-
Mohammadpoor-Baltork, I.1
Khosropour, A.R.2
-
23
-
-
0035796424
-
Bismuth(III) salts as convenient and efficient catalysts for the selective acetylation and benzoylation of alcohols and phenols
-
(b) Mohammadpoor-Baltork, I.; Aliyan, H.; Khosropour, A.R. Bismuth(III) salts as convenient and efficient catalysts for the selective acetylation and benzoylation of alcohols and phenols. Tetrahedron 2001, 57, 5851;
-
(2001)
Tetrahedron
, vol.57
, pp. 5851
-
-
Mohammadpoor-Baltork, I.1
Aliyan, H.2
Khosropour, A.R.3
-
24
-
-
0034819766
-
A convenient and chemoselective acetylation and formylation of alcohols and phenols using acetic acid and ethyl formate in the presence of Bi(III) salts
-
(c) Mohammadpoor-Baltork, I.; Khosropour, A.R.; Aliyan, H. A convenient and chemoselective acetylation and formylation of alcohols and phenols using acetic acid and ethyl formate in the presence of Bi(III) salts. J. Chem. Research (S) 2001, 7, 780;
-
(2001)
J. Chem. Research (S)
, vol.7
, pp. 780
-
-
Mohammadpoor-Baltork, I.1
Khosropour, A.R.2
Aliyan, H.3
-
25
-
-
0742297280
-
3 and catalyzed conversions of epoxides to thiiranes with ammonium thiocyanate and thiourea under non-aqueous conditions
-
3 and catalyzed conversions of epoxides to thiiranes with ammonium thiocyanate and thiourea under non-aqueous conditions. Molecules 2001, 6, 996;
-
(2001)
Molecules
, vol.6
, pp. 996
-
-
Mohammadpoor-Baltork, I.1
Khosropour, A.R.2
-
26
-
-
2442679796
-
Bi(III) salts as new catalysts for the selective conversion of trimethylsilyl and tetrahydropyranyl ethers to their corresponding acetates and formates
-
(e) Mohammadpoor-Baltork, I.; Khosropour, A.R. Bi(III) salts as new catalysts for the selective conversion of trimethylsilyl and tetrahydropyranyl ethers to their corresponding acetates and formates. Synth. Commun. 2001, 21, 3411.
-
(2001)
Synth. Commun.
, vol.21
, pp. 3411
-
-
Mohammadpoor-Baltork, I.1
Khosropour, A.R.2
-
27
-
-
0036134488
-
Bismuth nitrate pentahydrate: A new and enviromentally benign reagent for guanidylation of N-benzoylthioureas
-
(a) Cunha, S.; Lima, B.R.; Souza, A.R. Bismuth nitrate pentahydrate: a new and enviromentally benign reagent for guanidylation of N-benzoylthioureas. Tetrahedron Lett. 2002, 43, 49;
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 49
-
-
Cunha, S.1
Lima, B.R.2
Souza, A.R.3
-
28
-
-
0037433944
-
Bismuth(III) nitrate pentahydrate: A convenient and selective reagent for conversion of thiocarbonyls to their carbonyl compounds
-
and references therein
-
(b) Mohammadpoor-Baltork, I.; Khodaei, M.M.; Nikoofar, K. Bismuth(III) nitrate pentahydrate: a convenient and selective reagent for conversion of thiocarbonyls to their carbonyl compounds. Tetrahedron Lett. 2003, 44, 591 and references therein.
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 591
-
-
Mohammadpoor-Baltork, I.1
Khodaei, M.M.2
Nikoofar, K.3
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