-
1
-
-
34548494813
-
Microwave-induced bismuth nitrate-catalyzed synthesis of dihydropyrimidones via Biginelli condensation under solventless conditions
-
10.1016/j.tetlet.2007.08.007 1:CAS:528:DC%2BD2sXhtVGisr7K
-
Banik BK, Reddy AT, Datta A, Mukhopadhyay C (2007) Microwave-induced bismuth nitrate-catalyzed synthesis of dihydropyrimidones via Biginelli condensation under solventless conditions. Tetrahedron Lett 48:7392-7394
-
(2007)
Tetrahedron Lett
, vol.48
, pp. 7392-7394
-
-
Banik, B.K.1
Reddy, A.T.2
Datta, A.3
Mukhopadhyay, C.4
-
2
-
-
8644234920
-
An efficient, high yield protocol for the one-pot synthesis of dihydropyrimidin-2(1H)-ones catalyzed by iodine
-
10.1016/j.tetlet.2004.10.021 1:CAS:528:DC%2BD2cXpsVKjsr8%3D
-
Bhosale RS, Bhosale SV, Bhosale SV, Wang T, Zubaidha PK (2004) An efficient, high yield protocol for the one-pot synthesis of dihydropyrimidin- 2(1H)-ones catalyzed by iodine. Tetrahedron Lett 45:9111-9113
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 9111-9113
-
-
Bhosale, R.S.1
Bhosale, S.V.2
Bhosale, S.V.3
Wang, T.4
Zubaidha, P.K.5
-
3
-
-
77952542304
-
Recent advances in multicomponent reactions for diversity- oriented synthesis
-
20392661 10.1016/j.cbpa.2010.03.003 1:CAS:528:DC%2BC3cXmvVWqsLk%3D
-
Biggs-Houck JE, Younai A, Shaw JT (2010) Recent advances in multicomponent reactions for diversity- oriented synthesis. Curr Opin Chem Biol 14:371-382
-
(2010)
Curr Opin Chem Biol
, vol.14
, pp. 371-382
-
-
Biggs-Houck, J.E.1
Younai, A.2
Shaw, J.T.3
-
4
-
-
0000176059
-
Aldehyde-urea derivatives of aceto- and oxaloacetic acids
-
Biginelli P (1893) Aldehyde-urea derivatives of aceto- and oxaloacetic acids. Gazz Chim Ital 23:360-413
-
(1893)
Gazz Chim Ital
, vol.23
, pp. 360-413
-
-
Biginelli, P.1
-
5
-
-
84873405546
-
Synthesis of novel dihydropyrimidin-2(1H)-ones derivatives using lipase and their antimicrobial activity
-
10.5267/j.ccl.2012.3.001 1:CAS:528:DC%2BC38Xhsl2iurzN
-
Borse BN, Borude VS, Shukla SR (2012) Synthesis of novel dihydropyrimidin-2(1H)-ones derivatives using lipase and their antimicrobial activity. Curr Chem Lett 1:59-68
-
(2012)
Curr Chem Lett
, vol.1
, pp. 59-68
-
-
Borse, B.N.1
Borude, V.S.2
Shukla, S.R.3
-
6
-
-
5144226547
-
A simplified green chemistry approach to the Biginelli reaction using 'Grindstone Chemistry'
-
10.1016/j.tetlet.2004.09.064 1:CAS:528:DC%2BD2cXotlSnurc%3D
-
Bose AK, Pednekar S, Ganguly SN, Chakraborty G, Manhas MS (2004) A simplified green chemistry approach to the Biginelli reaction using 'Grindstone Chemistry'. Tetrahedron Lett 45:8351-8353
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 8351-8353
-
-
Bose, A.K.1
Pednekar, S.2
Ganguly, S.N.3
Chakraborty, G.4
Manhas, M.S.5
-
7
-
-
21044431756
-
Serum albumin-catalyzed trigger system by using a tandem kemp elimination/b-elimination reaction
-
15800865 10.1002/cbic.200400255 1:CAS:528:DC%2BD2MXksFajs7c%3D
-
Boucher G, Sylvain R, Fargeas V, Dintinger T, Mathe-Allainmat M, Lebreton J, Tellier C (2005) Serum albumin-catalyzed trigger system by using a tandem kemp elimination/b-elimination reaction. ChemBioChem 6:807-810
-
(2005)
ChemBioChem
, vol.6
, pp. 807-810
-
-
Boucher, G.1
Sylvain, R.2
Fargeas, V.3
Dintinger, T.4
Mathe-Allainmat, M.5
Lebreton, J.6
Tellier, C.7
-
8
-
-
70449517106
-
Synthesis of 3,4-dihydropyrimidin-2-ones (DHPMs) using mesoporous aluminosilicate (AlKIT-5) catalyst with cage type pore structure
-
10.1016/j.tet.2009.10.074
-
Chari MA, Mano A, Selvan ST, Mukkanti K, Vinu A (2009) Synthesis of 3,4-dihydropyrimidin-2-ones (DHPMs) using mesoporous aluminosilicate (AlKIT-5) catalyst with cage type pore structure. Tetrahedron 65:10608-10611
-
(2009)
Tetrahedron
, vol.65
, pp. 10608-10611
-
-
Chari, M.A.1
Mano, A.2
Selvan, S.T.3
Mukkanti, K.4
Vinu, A.5
-
9
-
-
63449103697
-
Calcium fluoride: An efficient and reusable catalyst for the synthesis of 3,4- dihydropyrimidin-2(1H)-ones and their corresponding 2(1H)thione: An improved high yielding protocol for the Biginelli reaction
-
10.1016/j.tetlet.2009.02.162 1:CAS:528:DC%2BD1MXjsl2gt7k%3D
-
Chitra S, Pandiarajan K (2009) Calcium fluoride: an efficient and reusable catalyst for the synthesis of 3,4- dihydropyrimidin-2(1H)-ones and their corresponding 2(1H)thione: an improved high yielding protocol for the Biginelli reaction. Tetrahedron Lett 50:2222-2224
-
(2009)
Tetrahedron Lett
, vol.50
, pp. 2222-2224
-
-
Chitra, S.1
Pandiarajan, K.2
-
10
-
-
84856717640
-
Expanding the organic toolbox: A guide to integrating biocatalysis in synthesis
-
22234546 10.1039/c2cs15286j 1:CAS:528:DC%2BC38XhsVajs78%3D
-
Clouthier CM, Pelletier JN (2012) Expanding the organic toolbox: a guide to integrating biocatalysis in synthesis. Chem Soc Rev 41:1585-1605
-
(2012)
Chem Soc Rev
, vol.41
, pp. 1585-1605
-
-
Clouthier, C.M.1
Pelletier, J.N.2
-
11
-
-
50549098579
-
A one-pot Biginelli synthesis of 3,4- dihydropyrimidin-2-(1H)-ones/ thiones catalyzed by triphenylphosphine as Lewis base
-
10.1016/j.tetlet.2008.08.016 1:CAS:528:DC%2BD1cXhtVyis7zO
-
Debache A, Amimour M, Belfaitah A, Rhouati S, Carboni B (2008) A one-pot Biginelli synthesis of 3,4- dihydropyrimidin-2-(1H)-ones/thiones catalyzed by triphenylphosphine as Lewis base. Tetrahedron Lett 49:6119-6121
-
(2008)
Tetrahedron Lett
, vol.49
, pp. 6119-6121
-
-
Debache, A.1
Amimour, M.2
Belfaitah, A.3
Rhouati, S.4
Carboni, B.5
-
12
-
-
33745621606
-
Phenylboronic acid as a mild and efficient catalyst for Biginelli reaction
-
10.1016/j.tetlet.2006.06.015 1:CAS:528:DC%2BD28XmvFeku78%3D
-
Debache A, Boumoud B, Amimour M, Belfaitah A, Rhouati S, Carboni B (2006) Phenylboronic acid as a mild and efficient catalyst for Biginelli reaction. Tetrahedron Lett 47:5697-5699
-
(2006)
Tetrahedron Lett
, vol.47
, pp. 5697-5699
-
-
Debache, A.1
Boumoud, B.2
Amimour, M.3
Belfaitah, A.4
Rhouati, S.5
Carboni, B.6
-
13
-
-
70450172774
-
The three-component Biginelli reaction: A combined experimental and theoretical mechanistic investigation
-
19670193 10.1002/chem.200900470
-
De Souza ROMA, da Penha ET, Milagre HMS, Garden SJ, Esteves PM, Eberlin MN, Antunes OAC (2009) The three-component Biginelli reaction: a combined experimental and theoretical mechanistic investigation. Chem Eur J 15:9799-9804
-
(2009)
Chem Eur J
, vol.15
, pp. 9799-9804
-
-
De Souza, R.1
Da Penha, E.T.2
Milagre, H.M.S.3
Garden, S.J.4
Esteves, P.M.5
Eberlin, M.N.6
Antunes, O.A.C.7
-
14
-
-
31544434530
-
Recent developments in isocyanide based multicomponent reactions in applied chemistry
-
16402771 10.1021/cr0505728
-
Dömling A (2006) Recent developments in isocyanide based multicomponent reactions in applied chemistry. Chem Rev 106:17-89
-
(2006)
Chem Rev
, vol.106
, pp. 17-89
-
-
Dömling, A.1
-
15
-
-
79953823660
-
Efficient synthesis of 3,4-dihydropyrimidin-2-ones in low melting tartaric acid-urea mixtures
-
10.1039/c1gc00009h 1:CAS:528:DC%2BC3MXkt1Khsbg%3D
-
Gore S, Baskaran S, Koenig B (2011) Efficient synthesis of 3,4-dihydropyrimidin-2-ones in low melting tartaric acid-urea mixtures. Green Chem 13:1009-1013
-
(2011)
Green Chem
, vol.13
, pp. 1009-1013
-
-
Gore, S.1
Baskaran, S.2
Koenig, B.3
-
16
-
-
78549294812
-
1,3-Dichloro-5,5-dimethylhydantoin as a novel and efficient homogeneous catalyst in Biginelli reaction
-
10.5012/bkcs.2010.31.11.3238 1:CAS:528:DC%2BC3cXhsFCitLrF
-
Hojati SF, Gholizadeh M, Haghdoust M, Shafiezadeh F (2010) 1,3-Dichloro-5,5-dimethylhydantoin as a novel and efficient homogeneous catalyst in Biginelli reaction. Bull Kor Chem Soc 31:3238-3240
-
(2010)
Bull Kor Chem Soc
, vol.31
, pp. 3238-3240
-
-
Hojati, S.F.1
Gholizadeh, M.2
Haghdoust, M.3
Shafiezadeh, F.4
-
17
-
-
0029793086
-
Off-the-shelf proteins that rival tailor-made antibodies as catalysts
-
8779715 10.1038/383060a0 1:CAS:528:DyaK28XlsV2jsLc%3D
-
Hollfelder F, Kirby AJ, Tawfik DS (1996) Off-the-shelf proteins that rival tailor-made antibodies as catalysts. Nature 383:60-63
-
(1996)
Nature
, vol.383
, pp. 60-63
-
-
Hollfelder, F.1
Kirby, A.J.2
Tawfik, D.S.3
-
18
-
-
70350474764
-
Applications of biotransformations and biocatalysis to complexity generation in organic synthesis
-
19847346 10.1039/b901172m 1:CAS:528:DC%2BD1MXht12ht7rP
-
Hudlicky T, Reed JW (2009) Applications of biotransformations and biocatalysis to complexity generation in organic synthesis. Chem Soc Rev 38:3117-3132
-
(2009)
Chem Soc Rev
, vol.38
, pp. 3117-3132
-
-
Hudlicky, T.1
Reed, J.W.2
-
19
-
-
43049095353
-
Recent advances in selective a1-adrenoreceptor antagonists as antihypertensive agents
-
18378462 10.1016/j.bmc.2008.02.091 1:CAS:528:DC%2BD1cXlvVSqtr0%3D
-
Jain KS, Bariwal JB, Kathiravan MK, Phoujdar MS, Sahne RS, Chauhan BS, Shah AK, Yadav MR (2008) Recent advances in selective a1-adrenoreceptor antagonists as antihypertensive agents. Bioorg Med Chem 16:4759-4800
-
(2008)
Bioorg Med Chem
, vol.16
, pp. 4759-4800
-
-
Jain, K.S.1
Bariwal, J.B.2
Kathiravan, M.K.3
Phoujdar, M.S.4
Sahne, R.S.5
Chauhan, B.S.6
Shah, A.K.7
Yadav, M.R.8
-
20
-
-
0030732273
-
A re-examination of the mechanism of the Biginelli dihydropyrimidine synthesis. Support for an N-acyliminium ion intermediate
-
11671828 10.1021/jo971010u 1:CAS:528:DyaK2sXmvVClt7k%3D
-
Kappe CO (1997) A re-examination of the mechanism of the Biginelli dihydropyrimidine synthesis. Support for an N-acyliminium ion intermediate. J Org Chem 62:7201-7204
-
(1997)
J Org Chem
, vol.62
, pp. 7201-7204
-
-
Kappe, C.O.1
-
21
-
-
0037925172
-
4-Aryldihydropyrimidines via the Biginelli condensation: Aza analogs of nifedipine-type calcium channel modulators
-
10.3390/30100001 1:CAS:528:DyaK1cXmvFKktw%3D%3D
-
Kappe CO (1998) 4-Aryldihydropyrimidines via the Biginelli condensation: aza analogs of nifedipine-type calcium channel modulators. Molecules 3:1-9
-
(1998)
Molecules
, vol.3
, pp. 1-9
-
-
Kappe, C.O.1
-
22
-
-
0034519777
-
Biologically active dihydropyrimidones of the Biginelli-type - A literature survey
-
11248403 10.1016/S0223-5234(00)01189-2 1:CAS:528:DC%2BD3MXoslWkuw%3D%3D
-
Kappe CO (2000) Biologically active dihydropyrimidones of the Biginelli-type - a literature survey. Eur J Med Chem 35:1043-1052
-
(2000)
Eur J Med Chem
, vol.35
, pp. 1043-1052
-
-
Kappe, C.O.1
-
23
-
-
34249094538
-
Isolation and identification of a novel strain of Pseudomonas chlororaphis capable of transforming isoeugenol to vanillin
-
17487530 10.1007/s00284-006-0627-z 1:CAS:528:DC%2BD2sXlsVGgu7o%3D
-
Kasana RC, Sharma UK, Sharma N, Sinha AK (2007) Isolation and identification of a novel strain of Pseudomonas chlororaphis capable of transforming isoeugenol to vanillin. Curr Microbiol 54:457-461
-
(2007)
Curr Microbiol
, vol.54
, pp. 457-461
-
-
Kasana, R.C.1
Sharma, U.K.2
Sharma, N.3
Sinha, A.K.4
-
24
-
-
23944504818
-
Synthesis of 4-aryl-7,7-dimethyl-1,2,3,4,5,6,7,8- octahydroquinazoline-2- one/thione-5-one derivatives and evaluation as antibacterials
-
16122583 10.1016/j.ejmech.2005.02.009 1:CAS:528:DC%2BD2MXpt1aqsrk%3D
-
Kidwai M, Saxena S, Khan MKR, Thukral SS (2005) Synthesis of 4-aryl-7,7-dimethyl-1,2,3,4,5,6,7,8- octahydroquinazoline-2-one/thione-5-one derivatives and evaluation as antibacterials. Eur J Med Chem 40:816-819
-
(2005)
Eur J Med Chem
, vol.40
, pp. 816-819
-
-
Kidwai, M.1
Saxena, S.2
Khan, M.K.R.3
Thukral, S.S.4
-
25
-
-
0032080371
-
An enantioselective fluorimetric assay for alcohol dehydrogenases using albumin-catalyzed-elimination of umbelliferone
-
9871718 10.1016/S0960-894X(98)00165-6 1:CAS:528:DyaK1cXjtlSnur8%3D
-
Klein G, Reymond JM (1998) An enantioselective fluorimetric assay for alcohol dehydrogenases using albumin-catalyzed-elimination of umbelliferone. Bioorg Med Chem Lett 8:1113-1116
-
(1998)
Bioorg Med Chem Lett
, vol.8
, pp. 1113-1116
-
-
Klein, G.1
Reymond, J.M.2
-
26
-
-
34249306161
-
An efficient bakers' yeast catalyzed synthesis of 3,4-dihydropyrimidin-2- (1H)-ones
-
10.1016/j.tetlet.2007.04.130 1:CAS:528:DC%2BD2sXmtVamsb4%3D
-
Kumar A, Maurya RA (2007) An efficient bakers' yeast catalyzed synthesis of 3,4-dihydropyrimidin-2-(1H)-ones. Tetrahedron Lett 48:4569-4571
-
(2007)
Tetrahedron Lett
, vol.48
, pp. 4569-4571
-
-
Kumar, A.1
Maurya, R.A.2
-
27
-
-
67651175852
-
Novel Biginelli dihydropyrimidines with potential anticancer activity: A parallel synthesis and CoMSIA study
-
10.1016/j.ejmech.2009.05.014
-
Kumar P, Sankar BR, Nasir G, Baig RB, Chandrashekaran S (2009) Novel Biginelli dihydropyrimidines with potential anticancer activity: a parallel synthesis and CoMSIA study. Eur J Med Chem 44:4192-4198
-
(2009)
Eur J Med Chem
, vol.44
, pp. 4192-4198
-
-
Kumar, P.1
Sankar, B.R.2
Nasir, G.3
Baig, R.B.4
Chandrashekaran, S.5
-
28
-
-
38549112888
-
Applications of lanthanide trichloride hydrates, prepared from mischmetall, in the Biginelli reaction
-
Lannou MI, Hélion F, Namy JL (2008) Applications of lanthanide trichloride hydrates, prepared from mischmetall, in the Biginelli reaction. Synlett 105-107
-
(2008)
Synlett
, pp. 105-107
-
-
Lannou Mi, H.1
-
30
-
-
0033615357
-
Small molecule inhibitor of mitotic spindle bipolarity identified in a phenotype-based screen
-
10542155 10.1126/science.286.5441.971 1:CAS:528:DyaK1MXntFaqu7o%3D
-
Mayer TU, Kapoor TM, Haggarty SJ, King RW, Schreiber SL, Mitchison TJ (1999) Small molecule inhibitor of mitotic spindle bipolarity identified in a phenotype-based screen. Science 286:971-974
-
(1999)
Science
, vol.286
, pp. 971-974
-
-
Mayer, T.U.1
Kapoor, T.M.2
Haggarty, S.J.3
King, R.W.4
Schreiber, S.L.5
Mitchison, T.J.6
-
31
-
-
84871657772
-
Pressure & urea-induced denaturation of bovine serum albumin: Considerations about protein heterogeneity
-
10.4236/ojbiphy.2012.21002
-
Norberto DR, Vieira JM, de Souza AR, Bispo JA, Bonafe CFS (2012) Pressure & urea-induced denaturation of bovine serum albumin: considerations about protein heterogeneity. Open J Biophys 2:4-14
-
(2012)
Open J Biophys
, vol.2
, pp. 4-14
-
-
Norberto, D.R.1
Vieira, J.M.2
De Souza, A.R.3
Bispo, J.A.4
Bonafe, C.F.S.5
-
32
-
-
39749093400
-
Synthesis of chiral pharmaceutical intermediates by biocatalysis
-
10.1016/j.ccr.2007.10.031 1:CAS:528:DC%2BD1cXislajsrk%3D
-
Patel RN (2008) Synthesis of chiral pharmaceutical intermediates by biocatalysis. Coord Chem Rev 252:659-701
-
(2008)
Coord Chem Rev
, vol.252
, pp. 659-701
-
-
Patel, R.N.1
-
33
-
-
33846197938
-
Biocatalysis for pharmaceutical intermediates: The future is now
-
17184862 10.1016/j.tibtech.2006.12.005 1:CAS:528:DC%2BD2sXnslGisg%3D%3D
-
Pollard DJ, Woodley JM (2007) Biocatalysis for pharmaceutical intermediates: the future is now. Trends Biotechnol 25:66-73
-
(2007)
Trends Biotechnol
, vol.25
, pp. 66-73
-
-
Pollard, D.J.1
Woodley, J.M.2
-
34
-
-
34548504530
-
Biginelli reaction in aqueous medium: A greener and sustainable approach to substituted 3,4-dihydropyrimidin-2(1H)-ones
-
10.1016/j.tetlet.2007.08.031 1:CAS:528:DC%2BD2sXhtVGju7bN
-
Polshettiwar V, Varma RS (2007) Biginelli reaction in aqueous medium: a greener and sustainable approach to substituted 3,4-dihydropyrimidin-2(1H)-ones. Tetrahedron Lett 48:7343-7346
-
(2007)
Tetrahedron Lett
, vol.48
, pp. 7343-7346
-
-
Polshettiwar, V.1
Varma, R.S.2
-
35
-
-
76349121035
-
Synthesis and lipase-catalysed enantioselective acylation studies on Ethyl-4-aryl-3,4- dihydropyrimidin-2(1H)-ones
-
1:CAS:528:DC%2BC3cXitVaiuro%3D
-
Prasad AK, Arya P, Bhatia S, Sharma RK, Singh R, Singh BK, Van der Eycken E, Singh R, Olsen CE, Parmar VS (2009) Synthesis and lipase-catalysed enantioselective acylation studies on Ethyl-4-aryl-3,4- dihydropyrimidin-2(1H)- ones. Ind J Chem 48B:1738-1748
-
(2009)
Ind J Chem
, vol.48
, pp. 1738-1748
-
-
Prasad, A.K.1
Arya, P.2
Bhatia, S.3
Sharma, R.K.4
Singh, R.5
Singh, B.K.6
Van Der Eycken, E.7
Singh, R.8
Olsen, C.E.9
Parmar, V.S.10
-
36
-
-
33644989059
-
A practical and green approach towards synthesis of dihydropyrimidinones: Using heteropoly acids as efficient catalysts
-
16464580 10.1016/j.bmcl.2006.01.087 1:CAS:528:DC%2BD28XislCgsrg%3D
-
Rafiee E, Jafari H (2006) A practical and green approach towards synthesis of dihydropyrimidinones: using heteropoly acids as efficient catalysts. Bioorg Med Chem Lett 16:2463-2466
-
(2006)
Bioorg Med Chem Lett
, vol.16
, pp. 2463-2466
-
-
Rafiee, E.1
Jafari, H.2
-
37
-
-
77949568046
-
A piperidinium triflate catalyzed Biginelli reaction
-
10.1016/j.tet.2010.02.067 1:CAS:528:DC%2BC3cXjvF2ltrg%3D
-
Ramalingan C, Park S-J, Lee I-S, Kwak Y-W (2010) A piperidinium triflate catalyzed Biginelli reaction. Tetrahedron 66:2987-2994
-
(2010)
Tetrahedron
, vol.66
, pp. 2987-2994
-
-
Ramalingan, C.1
Park, S.-J.2
Lee, I.-S.3
Kwak, Y.-W.4
-
38
-
-
33846828574
-
Enzyme promiscuity: First protein-catalyzed Morita-Baylis-Hillman reaction
-
10.1016/j.tetlet.2007.01.063 1:CAS:528:DC%2BD2sXhsFyrsLk%3D
-
Reetz MT, Mondire R, Carballeira JD (2007) Enzyme promiscuity: first protein-catalyzed Morita-Baylis-Hillman reaction. Tetrahedron Lett 48:1679-1681
-
(2007)
Tetrahedron Lett
, vol.48
, pp. 1679-1681
-
-
Reetz, M.T.1
Mondire, R.2
Carballeira, J.D.3
-
39
-
-
0032412508
-
Comparison of antibody and albumin catalyzed hydrolysis of steroidal p-Nitrophenylcarbonates
-
10214695 10.1007/BF02787707 1:CAS:528:DyaK1MXisVelurs%3D
-
Riva S, Mendozza M, Carrea G, Chattopadhay P, Tramontano A (1998) Comparison of antibody and albumin catalyzed hydrolysis of steroidal p-Nitrophenylcarbonates. Appl Biochem Biotechnol 75:33-44
-
(1998)
Appl Biochem Biotechnol
, vol.75
, pp. 33-44
-
-
Riva, S.1
Mendozza, M.2
Carrea, G.3
Chattopadhay, P.4
Tramontano, A.5
-
40
-
-
78651512142
-
Enantioselective organocatalytic Biginelli reaction: Dependence of the catalyst on Sterics, hydrogen bonding, and reinforced chirality
-
21192642 10.1021/jo101717m 1:CAS:528:DC%2BC3cXhs1ensrvF
-
Saha S, Moorthy JN (2011) Enantioselective organocatalytic Biginelli reaction: dependence of the catalyst on Sterics, hydrogen bonding, and reinforced chirality. J Org Chem 76:396-402
-
(2011)
J Org Chem
, vol.76
, pp. 396-402
-
-
Saha, S.1
Moorthy, J.N.2
-
41
-
-
79251531635
-
Multienzyme-catalyzed processes: Next- generation biocatalysis
-
10.1021/op1002159 1:CAS:528:DC%2BC3cXhsFShtbrP
-
Santacoloma PA, Sin G, Gernaey KV, Woodley JM (2011) Multienzyme- catalyzed processes: next- generation biocatalysis. Org Process Res Develop 15:203-212
-
(2011)
Org Process Res Develop
, vol.15
, pp. 203-212
-
-
Santacoloma, P.A.1
Sin, G.2
Gernaey, K.V.3
Woodley, J.M.4
-
42
-
-
0035843170
-
Industrial biocatalysis today and tomorrow
-
11196655 10.1038/35051736 1:CAS:528:DC%2BD3MXlvFWhug%3D%3D
-
Schmid A, Dordick JS, Hauer B, Kiener A, Wubbolts M, Witholt B (2001) Industrial biocatalysis today and tomorrow. Nature 409:258-268
-
(2001)
Nature
, vol.409
, pp. 258-268
-
-
Schmid, A.1
Dordick, J.S.2
Hauer, B.3
Kiener, A.4
Wubbolts, M.5
Witholt, B.6
-
43
-
-
0034700664
-
Synthesis and reactions of Biginelli-compounds. Part 23. chemoenzymatic syntheses of enantiomerically pure 4-aryl-3,4-dihydropyrimidin-2(1H)-ones
-
10.1039/b006372j
-
Schnell B, Krenn W, Faber K, Kappe CO (2000) Synthesis and reactions of Biginelli-compounds. Part 23. chemoenzymatic syntheses of enantiomerically pure 4-aryl-3,4-dihydropyrimidin-2(1H)-ones. J Chem Soc Perkin Trans 1:4382-4389
-
(2000)
J Chem Soc Perkin Trans
, vol.1
, pp. 4382-4389
-
-
Schnell, B.1
Krenn, W.2
Faber, K.3
Kappe, C.O.4
-
44
-
-
79954608575
-
2: Synthesis of aryl ketone or aldehydes via sequential dehydration-oxidative C = C cleavage
-
10.1007/s10562-010-0542-6 1:CAS:528:DC%2BC3MXhtVGjtA%3D%3D
-
2: synthesis of aryl ketone or aldehydes via sequential dehydration-oxidative C = C cleavage. Catal Lett 141:616-622
-
(2011)
Catal Lett
, vol.141
, pp. 616-622
-
-
Sharma, N.1
Sharma, U.K.2
Salwan, R.3
Kasana, R.C.4
Sinha, A.K.5
-
45
-
-
79955449980
-
First bovine serum albumin- promoted synthesis of enones, cinnamic acids and coumarins in ionic liquid: An insight into the role of protein impurities in porcine pancreas lipase for olefinic bond formation
-
10.1002/adsc.201000870 1:CAS:528:DC%2BC3MXltVGmt7k%3D
-
Sharma N, Sharma UK, Kumar R, Kumar R, Katoch N, Sinha AK (2011b) First bovine serum albumin- promoted synthesis of enones, cinnamic acids and coumarins in ionic liquid: an insight into the role of protein impurities in porcine pancreas lipase for olefinic bond formation. Adv Synth Catal 353:871-878
-
(2011)
Adv Synth Catal
, vol.353
, pp. 871-878
-
-
Sharma, N.1
Sharma, U.K.2
Kumar, R.3
Kumar, R.4
Katoch, N.5
Sinha, A.K.6
-
46
-
-
84867541172
-
3) ionic liquid triggered multicomponent Biginelli reaction for the efficient synthesis of dihydropyrimidinones
-
10.1039/c2ra22037g 1:CAS:528:DC%2BC38XhsFSrtb3J
-
3) ionic liquid triggered multicomponent Biginelli reaction for the efficient synthesis of dihydropyrimidinones. RSC Adv 2:10648-10651
-
(2012)
RSC Adv
, vol.2
, pp. 10648-10651
-
-
Sharma, N.1
Sharma, U.K.2
Kumar, R.3
Richa, A.K.4
Sinha, A.K.5
-
48
-
-
84855347927
-
Efficient synthesis of hydroxystyrenes via biocatalytic decarboxylation/deacetylation of substituted cinnamic acids by newly isolated Pantoea agglomerans strains
-
10.1002/jsfa.4616 1:CAS:528:DC%2BC38XitVCmsg%3D%3D
-
Sharma UK, Sharma N, Salwan R, Kumar R, Kasana RC, Sinha AK (2012b) Efficient synthesis of hydroxystyrenes via biocatalytic decarboxylation/ deacetylation of substituted cinnamic acids by newly isolated Pantoea agglomerans strains. J Sci Food Agric 92:610-616
-
(2012)
J Sci Food Agric
, vol.92
, pp. 610-616
-
-
Sharma, U.K.1
Sharma, N.2
Salwan, R.3
Kumar, R.4
Kasana, R.C.5
Sinha, A.K.6
-
49
-
-
77249090233
-
Brønsted base-catalyzed one-pot three-component Biginelli-type reaction: An efficient synthesis of 4,5,6-triaryl-3,4-dihydropyrimidin-2(1H)-one and mechanistic study
-
20085235 10.1021/jo902394y 1:CAS:528:DC%2BC3cXnvFSltw%3D%3D
-
Shen ZL, Xu XP, Ji SJ (2010) Brønsted base-catalyzed one-pot three-component Biginelli-type reaction: an efficient synthesis of 4,5,6-triaryl-3,4-dihydropyrimidin-2(1H)-one and mechanistic study. J Org Chem 75:1162-1167
-
(2010)
J Org Chem
, vol.75
, pp. 1162-1167
-
-
Shen, Z.L.1
Xu, X.P.2
Ji, S.J.3
-
50
-
-
66949121347
-
Investigation of lipase-catalyzed Michael-type carbon-carbon bond formations
-
10.1016/j.tet.2009.05.042 1:CAS:528:DC%2BD1MXntlSmsrk%3D
-
Strohmeier GA, Sovic T, Steinkellner G, Hartner FS, Andryushkova A, Purkarthofer T, Glieder A, Gruber K, Griengl H (2009) Investigation of lipase-catalyzed Michael-type carbon-carbon bond formations. Tetrahedron 65:5663-5668
-
(2009)
Tetrahedron
, vol.65
, pp. 5663-5668
-
-
Strohmeier, G.A.1
Sovic, T.2
Steinkellner, G.3
Hartner, F.S.4
Andryushkova, A.5
Purkarthofer, T.6
Glieder, A.7
Gruber, K.8
Griengl, H.9
-
51
-
-
41949141456
-
Biginelli reactions catalyzed by hydrazine type organocatalyst
-
10.1016/j.tetlet.2008.03.080 1:CAS:528:DC%2BD1cXkvV2qsbg%3D
-
Suzuki I, Iwata Y, Takeda K (2008) Biginelli reactions catalyzed by hydrazine type organocatalyst. Tetrahedron Lett 49:3238-3241
-
(2008)
Tetrahedron Lett
, vol.49
, pp. 3238-3241
-
-
Suzuki, I.1
Iwata, Y.2
Takeda, K.3
-
52
-
-
74049112279
-
Synthesis of 3,4-dihydropyrimidin-2(1H)-ones and 1,4-dihydropyridines using ammonium carbonate in water
-
10.1016/j.tetlet.2009.12.098 1:CAS:528:DC%2BC3cXhtVGlsbo%3D
-
Tamaddon F, Razmi Z, Jafari AA (2010) Synthesis of 3,4-dihydropyrimidin- 2(1H)-ones and 1,4-dihydropyridines using ammonium carbonate in water. Tetrahedron Lett 51:1187-1189
-
(2010)
Tetrahedron Lett
, vol.51
, pp. 1187-1189
-
-
Tamaddon, F.1
Razmi, Z.2
Jafari, A.A.3
-
53
-
-
0016841211
-
Bovine serum albumin as a catalyst. II. Characterization of the kinetics
-
1133402 10.1021/ja00840a055 1:CAS:528:DyaE2MXhsFSqsLg%3D
-
Taylor RP, Chau V, Bryner C, Berga S (1975) Bovine serum albumin as a catalyst. II. Characterization of the kinetics. J Am Chem Soc 97:1934-1943
-
(1975)
J Am Chem Soc
, vol.97
, pp. 1934-1943
-
-
Taylor, R.P.1
Chau, V.2
Bryner, C.3
Berga, S.4
-
54
-
-
34447136294
-
Biocatalysis in ionic liquids
-
17564484 10.1021/cr050946x
-
Van Rantwijk F, Sheldon RA (2007) Biocatalysis in ionic liquids. Chem Rev 107:2757-2785
-
(2007)
Chem Rev
, vol.107
, pp. 2757-2785
-
-
Van Rantwijk, F.1
Sheldon, R.A.2
-
56
-
-
79952575661
-
Candida antarctica lipase B-catalyzed the unprecedented three-component Hantzsch-type reaction of aldehyde with acetamide and 1,3-dicarbonyl compounds in non-aqueous solvent
-
10.1016/j.tet.2011.01.045 1:CAS:528:DC%2BC3MXjtFGms74%3D
-
Wang J-L, Liu B-K, Yin C, Wu Q, Lin X-F (2011) Candida antarctica lipase B-catalyzed the unprecedented three-component Hantzsch-type reaction of aldehyde with acetamide and 1,3-dicarbonyl compounds in non-aqueous solvent. Tetrahedron 67:2689-2692
-
(2011)
Tetrahedron
, vol.67
, pp. 2689-2692
-
-
Wang, J.-L.1
Liu, B.-K.2
Yin, C.3
Wu, Q.4
Lin, X.-F.5
-
57
-
-
0344861909
-
Transition-metal-mediated cascade reactions: C, C- dicyclopropylmethylamines by way of double C, C-σ-bond insertion into bicyclobutanes
-
14640630 10.1021/ja038623a 1:CAS:528:DC%2BD3sXoslWmsro%3D
-
Wipf P, Stephenson CRJ, Okumura K (2003) Transition-metal-mediated cascade reactions: C, C-dicyclopropylmethylamines by way of double C, C-σ-bond insertion into bicyclobutanes. J Am Chem Soc 125:14694-14695
-
(2003)
J Am Chem Soc
, vol.125
, pp. 14694-14695
-
-
Wipf, P.1
Stephenson, C.R.J.2
Okumura, K.3
-
58
-
-
0041967088
-
Synthesis and in vitro calcium antagonist activity of 4-aryl-7,7-dimethyl/1,7,7-trimethyl-1,2,3,4,5,6,7,8-octahydroquinazoline-2, 5-dione derivatives
-
12595033 10.1016/S0014-827X(02)00009-5 1:CAS:528:DC%2BD3sXht1Krs7c%3D
-
Yarim M, Saraç S, Kiliç FS, Erol K (2003) Synthesis and in vitro calcium antagonist activity of 4-aryl-7,7-dimethyl/1,7,7-trimethyl-1,2,3, 4,5,6,7,8-octahydroquinazoline-2,5-dione derivatives. Farmaco 58:17-24
-
(2003)
Farmaco
, vol.58
, pp. 17-24
-
-
Yarim, M.1
Saraç, S.2
Kiliç, F.S.3
Erol, K.4
-
59
-
-
34249284144
-
One-pot synthesis of 3,4-dihydropyrimidin-2(1H)-ones using chloroacetic acid as catalyst
-
17490874 10.1016/j.bmcl.2006.12.068 1:CAS:528:DC%2BD2sXmtValsbY%3D
-
Yu Y, Liu C, Luo G (2007) One-pot synthesis of 3,4-dihydropyrimidin-2(1H) -ones using chloroacetic acid as catalyst. Bioorg Med Chem Lett 17:3508-3510
-
(2007)
Bioorg Med Chem Lett
, vol.17
, pp. 3508-3510
-
-
Yu, Y.1
Liu, C.2
Luo, G.3
-
61
-
-
77958485628
-
A highly efficient synthesis of telaprevir by strategic use of biocatalysis and multicomponent reactions
-
10.1039/c0cc02823a 1:CAS:528:DC%2BC3cXhtlantrvL
-
Znabet A, Polak MM, Janssen E, de Kanter FJJ, Turner NJ, Orru RVA, Ruijter E (2010a) A highly efficient synthesis of telaprevir by strategic use of biocatalysis and multicomponent reactions. Chem Commun 46:7918-7920
-
(2010)
Chem Commun
, vol.46
, pp. 7918-7920
-
-
Znabet, A.1
Polak, M.M.2
Janssen, E.3
De Kanter, F.J.J.4
Turner, N.J.5
Orru, R.V.A.6
Ruijter, E.7
-
62
-
-
77957841915
-
Asymmetric synthesis of synthetic alkaloids by a tandem biocatalysis/Ugi/Pictet-Spengler-type cyclization sequence
-
10.1039/c0cc02938f 1:CAS:528:DC%2BC3cXht1Omtr%2FK
-
Znabet A, Zonneveld J, Janssen E, de Kanter FJJ, Helliwell M, Turner NJ, Ruijter E, Orru RVA (2010b) Asymmetric synthesis of synthetic alkaloids by a tandem biocatalysis/Ugi/Pictet-Spengler-type cyclization sequence. Chem Commun 46:7706-7708
-
(2010)
Chem Commun
, vol.46
, pp. 7706-7708
-
-
Znabet, A.1
Zonneveld, J.2
Janssen, E.3
De Kanter, F.J.J.4
Helliwell, M.5
Turner, N.J.6
Ruijter, E.7
Orru, R.V.A.8
|