-
1
-
-
84861048815
-
Continuous Flow Synthesis. A Pharma Perspective
-
Sanz, L. M.; Susanne, F. Continuous Flow Synthesis. A Pharma Perspective J. Med. Chem. 2012, 55, 4062-4098
-
(2012)
J. Med. Chem.
, vol.55
, pp. 4062-4098
-
-
Sanz, L.M.1
Susanne, F.2
-
2
-
-
80051586082
-
The Flow Synthesis of Heterocycles for Natural Product and Medicinal Chemistry Applications
-
Baumann, M.; Baxendale, I. R.; Ley, S. V. The Flow Synthesis of Heterocycles for Natural Product and Medicinal Chemistry Applications Mol. Diversity 2011, 15, 613-630
-
(2011)
Mol. Diversity
, vol.15
, pp. 613-630
-
-
Baumann, M.1
Baxendale, I.R.2
Ley, S.V.3
-
3
-
-
84857174482
-
Continuous Flow Reactors: A Perspective
-
Wiles, C.; Watts, P. Continuous Flow Reactors: A Perspective Green Chem. 2012, 14, 38-54
-
(2012)
Green Chem.
, vol.14
, pp. 38-54
-
-
Wiles, C.1
Watts, P.2
-
4
-
-
79953702549
-
Ten Key Issues in Modern Flow Chemistry
-
Wegner, J.; Ceylan, S.; Kirschning, A. Ten Key Issues in Modern Flow Chemistry Chem. Commun. 2011, 47, 4583-4592
-
(2011)
Chem. Commun.
, vol.47
, pp. 4583-4592
-
-
Wegner, J.1
Ceylan, S.2
Kirschning, A.3
-
5
-
-
78649393215
-
The Sulphonamide Motif as a Synthetic Tool
-
Wilden, J. D. The Sulphonamide Motif as a Synthetic Tool J. Chem. Res. 2010, 541-548
-
(2010)
J. Chem. Res.
, pp. 541-548
-
-
Wilden, J.D.1
-
6
-
-
0041919643
-
Protease Inhibitors of the Sulfonamide Type: Anticancer, Antiinflammatory, and Antiviral Agents
-
Supuran, C.T.; Casini, A.; Scozzafava, A. Protease Inhibitors of the Sulfonamide Type: Anticancer, Antiinflammatory, and Antiviral Agents Med. Res. Rev. 2003, 5, 535-558
-
(2003)
Med. Res. Rev.
, vol.5
, pp. 535-558
-
-
Supuran . C, T.1
Casini, A.2
Scozzafava, A.3
-
7
-
-
0013209248
-
Anticancer and Antiviral Sulfonamides
-
Scozzafava, A.; Owa, T.; Mastrolorenzo, A.; Supuran, C. T. Anticancer and Antiviral Sulfonamides Curr. Med. Chem. 2003, 10, 925-953
-
(2003)
Curr. Med. Chem.
, vol.10
, pp. 925-953
-
-
Scozzafava, A.1
Owa, T.2
Mastrolorenzo, A.3
Supuran, C.T.4
-
8
-
-
32144444850
-
A Convenient Preparation of Heteroaryl Sulfonamides and Sulfonyl Fluorides from Heteroaryl Thiols
-
Wright, S. W.; Hallstrom, K. N. A Convenient Preparation of Heteroaryl Sulfonamides and Sulfonyl Fluorides from Heteroaryl Thiols J. Org. Chem. 2006, 71, 1080-1084
-
(2006)
J. Org. Chem.
, vol.71
, pp. 1080-1084
-
-
Wright, S.W.1
Hallstrom, K.N.2
-
9
-
-
27744441767
-
N -Sulfonylbenzotriazoles as Advantageous Reagents for C-Sulfonylation
-
Katritzky, A. R.; Abdel-Fattah, A. A. A.; Vakulenko, A. V.; Tao, H. N -Sulfonylbenzotriazoles as Advantageous Reagents for C-Sulfonylation J. Org. Chem. 2005, 70, 9191-9197
-
(2005)
J. Org. Chem.
, vol.70
, pp. 9191-9197
-
-
Katritzky, A.R.1
Abdel-Fattah, A.A.A.2
Vakulenko, A.V.3
Tao, H.4
-
10
-
-
0942276310
-
Direct Synthesis of Sulfonamides and Activated Sulfonate Esters from Sulfonic Acids
-
Caddick, S.; Wilden, J. D.; Judd, D. B. Direct Synthesis of Sulfonamides and Activated Sulfonate Esters from Sulfonic Acids J. Am. Chem. Soc. 2004, 126, 1024-1025
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 1024-1025
-
-
Caddick, S.1
Wilden, J.D.2
Judd, D.B.3
-
11
-
-
0142121704
-
Facile One-Pot Synthesis of Aromatic and Heteroaromatic Sulfonamides
-
Pandya, R.; Murashima, T.; Tedeschi, L.; Barrett, A. G. M. Facile One-Pot Synthesis of Aromatic and Heteroaromatic Sulfonamides J. Org. Chem. 2003, 68, 8274-2876
-
(2003)
J. Org. Chem.
, vol.68
, pp. 8274-2876
-
-
Pandya, R.1
Murashima, T.2
Tedeschi, L.3
Barrett, A.G.M.4
-
12
-
-
0141452066
-
Nitrophenol Resins for Facile Amide and Sulfonamide Library Synthesis
-
Lee, J. V.; Louie, Y. Q.; Walsh, D. P.; Chang, Y.-T. Nitrophenol Resins for Facile Amide and Sulfonamide Library Synthesis J. Comb. Chem. 2003, 5, 330-335
-
(2003)
J. Comb. Chem.
, vol.5
, pp. 330-335
-
-
Lee, J.V.1
Louie, Y.Q.2
Walsh, D.P.3
Chang, Y.-T.4
-
13
-
-
0036421987
-
Catalytic Arylation of Sulfamoyl Chlorides: A Practical Synthesis of Sulfonamides
-
Frost, C. G.; Hartley, J. P.; Griffin, D. Catalytic Arylation of Sulfamoyl Chlorides: A Practical Synthesis of Sulfonamides Synlett 2002, 11, 1928-1930
-
(2002)
Synlett
, vol.11
, pp. 1928-1930
-
-
Frost, C.G.1
Hartley, J.P.2
Griffin, D.3
-
14
-
-
0006009372
-
Preparation of Nonsymmetrical p -Benzoquinone Diimides for Evaluation as Protein Cleavage Reagents
-
Holmes, T. J. J.; Lawton, R. G. Preparation of Nonsymmetrical p -Benzoquinone Diimides for Evaluation as Protein Cleavage Reagents J. Org. Chem. 1983, 48, 3146-3150
-
(1983)
J. Org. Chem.
, vol.48
, pp. 3146-3150
-
-
Holmes, T.J.J.1
Lawton, R.G.2
-
15
-
-
6844222490
-
The Reactions of Aliphatic Acid Chlorides
-
Sonntag, N. O. V. The Reactions of Aliphatic Acid Chlorides Chem. Rev. 1953, 52, 237-476
-
(1953)
Chem. Rev.
, vol.52
, pp. 237-476
-
-
Sonntag, N.O.V.1
-
16
-
-
0037050428
-
Novel 1,4-Benzodiazepines from Acylnitroso-Derived Hetero-Diels-Alder Cycloadducts
-
Surman, M. D.; Mulvihill, M. J.; Miller, M. J. Novel 1,4-Benzodiazepines from Acylnitroso-Derived Hetero-Diels-Alder Cycloadducts Org. Lett. 2002, 4, 139-141
-
(2002)
Org. Lett.
, vol.4
, pp. 139-141
-
-
Surman, M.D.1
Mulvihill, M.J.2
Miller, M.J.3
-
17
-
-
0037375844
-
Synthesis and Biological Evaluation of Substituted 2-Sulfonyl-Phenyl-3- Phenyl-Indoles: A New Series of Selective COX-2 Inhibitors
-
Hu, W.; Guo, Z.; Chu, F.; Bai, A.; Yi, X.; Cheng, G.; Li, J. Synthesis and Biological Evaluation of Substituted 2-Sulfonyl-Phenyl-3-Phenyl-Indoles: A New Series of Selective COX-2 Inhibitors Bioorg. Med. Chem. 2003, 11, 1153-1160
-
(2003)
Bioorg. Med. Chem.
, vol.11
, pp. 1153-1160
-
-
Hu, W.1
Guo, Z.2
Chu, F.3
Bai, A.4
Yi, X.5
Cheng, G.6
Li, J.7
-
18
-
-
1042284378
-
Indium-Mediated Reformatsky-Type Reaction of β-Aminovinyl Chlorodifluoromethyl Ketones with Heteroaryl Aldehydes
-
Medebielle, M.; Onomura, O.; Keirouz, R.; Okada, E.; Yano, H.; Terauchi, T. Indium-Mediated Reformatsky-Type Reaction of β-Aminovinyl Chlorodifluoromethyl Ketones with Heteroaryl Aldehydes Synthesis 2002, 17, 2601-2608
-
(2002)
Synthesis
, vol.17
, pp. 2601-2608
-
-
Medebielle, M.1
Onomura, O.2
Keirouz, R.3
Okada, E.4
Yano, H.5
Terauchi, T.6
-
19
-
-
66249135257
-
Design and Synthesis of Small Molecule Glycerol 3-Phosphate Acyltransferase Inhibitors
-
Wydysh, E. A.; Medghalchi, S. M.; Vadlamudi, A.; Townsend, C. A. Design and Synthesis of Small Molecule Glycerol 3-Phosphate Acyltransferase Inhibitors J. Med. Chem. 2009, 52, 3317-3327
-
(2009)
J. Med. Chem.
, vol.52
, pp. 3317-3327
-
-
Wydysh, E.A.1
Medghalchi, S.M.2
Vadlamudi, A.3
Townsend, C.A.4
-
20
-
-
0032978655
-
Selective Monodesulfonylation of N, N -Disulfonylarylamines with Tetrabutylammonium Fluoride
-
Yasuhara, A.; Kameda, M.; Sakamoto, T. Selective Monodesulfonylation of N, N -Disulfonylarylamines with Tetrabutylammonium Fluoride Chem. Pharm. Bull. 1999, 47, 809-812
-
(1999)
Chem. Pharm. Bull.
, vol.47
, pp. 809-812
-
-
Yasuhara, A.1
Kameda, M.2
Sakamoto, T.3
-
21
-
-
33748058169
-
A Facile, Environmentally Benign Sulfonamide Synthesis in Water
-
Deng, X.; Mani, N. S. A Facile, Environmentally Benign Sulfonamide Synthesis in Water Green Chem. 2006, 8, 835-838
-
(2006)
Green Chem.
, vol.8
, pp. 835-838
-
-
Deng, X.1
Mani, N.S.2
-
22
-
-
34249936288
-
Fully Automated Flow-Through Synthesis of Secondary Sulfonamides in a Binary Reactor System
-
Griffiths-Jones, C. M.; Hopkin, M. D.; Jönsson, D.; Ley, S. V.; Tapolczay, D. J.; Vickerstaffe, E.; Ladlow, M. Fully Automated Flow-Through Synthesis of Secondary Sulfonamides in a Binary Reactor System J. Comb. Chem. 2007, 9, 422-430
-
(2007)
J. Comb. Chem.
, vol.9
, pp. 422-430
-
-
Griffiths-Jones, C.M.1
Hopkin, M.D.2
Jönsson, D.3
Ley, S.V.4
Tapolczay, D.J.5
Vickerstaffe, E.6
Ladlow, M.7
-
23
-
-
79960247989
-
Synthesis of a Drug-Like Focused Library of Trisubstituted Pyrrolidines Using Integrated Flow Chemistry and Batch Methods
-
Baumann, M.; Baxendale, I. R.; Kuratli, C.; Ley, S. V.; Martin, R. E.; Schneider, J. Synthesis of a Drug-Like Focused Library of Trisubstituted Pyrrolidines Using Integrated Flow Chemistry and Batch Methods ACS Comb. Science 2011, 13, 405-413
-
(2011)
ACS Comb. Science
, vol.13
, pp. 405-413
-
-
Baumann, M.1
Baxendale, I.R.2
Kuratli, C.3
Ley, S.V.4
Martin, R.E.5
Schneider, J.6
-
24
-
-
84860740545
-
Continuous Flow Synthesis and Scale-up of Glycine- and Taurine-Conjugated Bile Salts
-
Venturoni, F.; Gioiello, A.; Sardella, R.; Natalini, B.; Pellicciari, R. Continuous Flow Synthesis and Scale-up of Glycine- and Taurine-Conjugated Bile Salts Org. Biomol. Chem. 2012, 10, 4109-15
-
(2012)
Org. Biomol. Chem.
, vol.10
, pp. 4109-4115
-
-
Venturoni, F.1
Gioiello, A.2
Sardella, R.3
Natalini, B.4
Pellicciari, R.5
-
25
-
-
34547280363
-
PEG-Assisted Solvent and Catalyst Free Synthesis of 3,4- Dihydropyrimidinones under Mild Reaction Conditions
-
Suman, L. J.; Sweety, S.; Bir, S. PEG-Assisted Solvent and Catalyst Free Synthesis of 3,4-Dihydropyrimidinones Under Mild Reaction Conditions Green Chem. 2007, 9, 740-741
-
(2007)
Green Chem.
, vol.9
, pp. 740-741
-
-
Suman, L.J.1
Sweety, S.2
Bir, S.3
-
26
-
-
50249168382
-
Improved Chemoselective, Ecofriendly Conditions for the Conversion of Primary Alkyl Halides into Nitroalkanes under PEG 400
-
Ballini, R.; Barboni, L.; Palmieri, A. Improved Chemoselective, Ecofriendly Conditions for the Conversion of Primary Alkyl Halides into Nitroalkanes Under PEG 400 Green Chem. 2008, 10, 1004-1006
-
(2008)
Green Chem.
, vol.10
, pp. 1004-1006
-
-
Ballini, R.1
Barboni, L.2
Palmieri, A.3
-
27
-
-
33645461921
-
Polyethylene Glycol as a Non-Ionic Liquid Solvent for Michael Addition Reaction of Amines to Conjugated Alkenes
-
Kumar, R.; Chaudhary, P.; Nimesh, S.; Chandra, R. Polyethylene Glycol as a Non-Ionic Liquid Solvent for Michael Addition Reaction of Amines to Conjugated Alkenes Green Chem. 2006, 8, 356-358
-
(2006)
Green Chem.
, vol.8
, pp. 356-358
-
-
Kumar, R.1
Chaudhary, P.2
Nimesh, S.3
Chandra, R.4
-
28
-
-
57249085654
-
Microwave-Accelerated Suzuki Cross-Coupling Reaction in Polyethylene Glycol (PEG)
-
Vasudevan, V. N.; Rajender, S. V. Microwave-Accelerated Suzuki Cross-Coupling Reaction in Polyethylene Glycol (PEG) Green Chem. 2001, 3, 146-148
-
(2001)
Green Chem.
, vol.3
, pp. 146-148
-
-
Vasudevan, V.N.1
Rajender, S.V.2
-
29
-
-
0012621976
-
Poly(ethylene glycol) (PEG) as a Reusable Solvent Medium for Organic Synthesis. Application in the Heck Reaction
-
Chandrasekhar, S.; Narsihmulu, C.; Sultana, S. S.; Reddy, N. R. K. Poly(ethylene glycol) (PEG) as a Reusable Solvent Medium for Organic Synthesis. Application in the Heck Reaction Org. Lett. 2002, 4, 4399-4401
-
(2002)
Org. Lett.
, vol.4
, pp. 4399-4401
-
-
Chandrasekhar, S.1
Narsihmulu, C.2
Sultana, S.S.3
Reddy, N.R.K.4
-
30
-
-
84877726971
-
-
U.S. Patent US2608507A.
-
Miller, C. U.S. Patent US2608507A, 1952.
-
(1952)
-
-
Miller, C.1
-
31
-
-
84877766714
-
-
Patent ES209068A1
-
Gonzalez, J. M. Patent ES209068A1, 1953.
-
(1953)
-
-
Gonzalez, J.M.1
|