-
1
-
-
85177098727
-
-
Fan, W.Q.; Katritzky, A.R. 1,2,3 Triazoles. In Comprehensive Heterocycle Chemistry II; Katritzky, A.R., Rees, C.W., Scriven, E.F.V., Eds.; Pergamon Press: New York, NY, USA, 1996; pp. 1-126.
-
Fan, W.Q.; Katritzky, A.R. 1,2,3 Triazoles. In Comprehensive Heterocycle Chemistry II; Katritzky, A.R., Rees, C.W., Scriven, E.F.V., Eds.; Pergamon Press: New York, NY, USA, 1996; Vol. pp. 1-126.
-
-
-
-
2
-
-
0037696408
-
1,2,3-Triazole formation under mild conditions via 1,3-dipolar cycloaddition of acetylenes with azides
-
Katritzky, A.R.; Zhang, Y.; Singh, S.K. 1,2,3-Triazole formation under mild conditions via 1,3-dipolar cycloaddition of acetylenes with azides. Heterocycles 2003, 60, 1225-1239.
-
(2003)
Heterocycles
, vol.60
, pp. 1225-1239
-
-
Katritzky, A.R.1
Zhang, Y.2
Singh, S.K.3
-
3
-
-
0028063421
-
1,2,3-Triazole-[2′,5′- bis-O-(tert-butyldimethylsilyl)-beta-D-ribofuranosyl]-3′-spiro-5"- (4"-amino-1″,2″-oxathiole 2″,2″-dioxide) (TSAO) analogues: Synthesis and anti-HIV-1 activity
-
Alvarez, R.; Velazquez, S.; San, R.; Aquaro, S.; De, C.E.; Perno, C.F.; Karlsson, A.; Balzarini, J.; Camarasa, M.J. 1,2,3-Triazole-[2′,5′- bis-O-(tert-butyldimethylsilyl)-beta-D-ribofuranosyl]-3′-spiro-5"- (4"-amino-1″,2″-oxathiole 2″,2″-dioxide) (TSAO) analogues: Synthesis and anti-HIV-1 activity. J. Med. Chem. 1994, 37, 4185-4194.
-
(1994)
J. Med. Chem
, vol.37
, pp. 4185-4194
-
-
Alvarez, R.1
Velazquez, S.2
San, R.3
Aquaro, S.4
De, C.E.5
Perno, C.F.6
Karlsson, A.7
Balzarini, J.8
Camarasa, M.J.9
-
4
-
-
0031791262
-
Regiospecific synthesis and anti-human immunodeficiency virus activity of novel 5-substituted N-alkylcarbamoyl and N, N-dialkylcarbamoyl 1,2,3-triazole-TSAO analogues
-
Velazquez, S.; Alvarez, R.; Perez, C.; Gago, F.; De C.E.; Balzarini, J.; Camarasa, J.M. Regiospecific synthesis and anti-human immunodeficiency virus activity of novel 5-substituted N-alkylcarbamoyl and N, N-dialkylcarbamoyl 1,2,3-triazole-TSAO analogues. Antiviral Chem. Chemother. 1998, 9, 481-489.
-
(1998)
Antiviral Chem. Chemother
, vol.9
, pp. 481-489
-
-
Velazquez, S.1
Alvarez, R.2
Perez, C.3
Gago, F.4
De, C.E.5
Balzarini, J.6
Camarasa, J.M.7
-
5
-
-
33746210083
-
Inhibitors of HIV-1 protease by using in situ click chemistry
-
Whiting, M.; Muldoon, J.; Lin, Y.C.; Silverman, S.M.; Lindstrom, W.; Olson, A.J.; Kolb, H.C.; Finn, M.G.; Sharpless, B.K.; Elder, J.H.; Fokin, V.V. Inhibitors of HIV-1 protease by using in situ click chemistry. Angew. Chem. Int. Ed. 2006, 45, 1435-1439.
-
(2006)
Angew. Chem. Int. Ed
, vol.45
, pp. 1435-1439
-
-
Whiting, M.1
Muldoon, J.2
Lin, Y.C.3
Silverman, S.M.4
Lindstrom, W.5
Olson, A.J.6
Kolb, H.C.7
Finn, M.G.8
Sharpless, B.K.9
Elder, J.H.10
Fokin, V.V.11
-
6
-
-
0345306644
-
Rapid diversity-oriented synthesis in microtiter plates for in situ screening of HIV protease inhibitors
-
Brik, A.; Muldoon, J.; Lin, Y.C.; Elder, J.C.; Goodsell, D.S.; Olson, A.J.; Fokin, V.V.; Sharpless, B.K.; Wong, C.H. Rapid diversity-oriented synthesis in microtiter plates for in situ screening of HIV protease inhibitors. Chem. Bio. Chem. 2003, 4, 1246-1248.
-
(2003)
Chem. Bio. Chem
, vol.4
, pp. 1246-1248
-
-
Brik, A.1
Muldoon, J.2
Lin, Y.C.3
Elder, J.C.4
Goodsell, D.S.5
Olson, A.J.6
Fokin, V.V.7
Sharpless, B.K.8
Wong, C.H.9
-
7
-
-
0034624685
-
-
Genin, M.J.; Allwine, D.A.; Anderson, D.J.; Barbachyn, M.R.; Emmert, D.M.; Garmon, S.A.; Graber, D.R.; Grega, K.C.; Hester, J.B.; Hutchinson, D.K.; Morris, J.; Reischer, R.J.; Ford, C.W.; Zurenko, G.E.; Hamel, J.C.; Schaadt, R.D.; Stapert, D.; Yagi, B.H. Substituent effects on the antibacterial activity of nitrogen-carbon-linked (azolylphenyl)oxazolidinones with expanded activity against the fastidious gram-negative organisms Haemophilus influenzae and Moraxella catarrhalis. J. Med. Chem. 2000, 43, 953-970.
-
Genin, M.J.; Allwine, D.A.; Anderson, D.J.; Barbachyn, M.R.; Emmert, D.M.; Garmon, S.A.; Graber, D.R.; Grega, K.C.; Hester, J.B.; Hutchinson, D.K.; Morris, J.; Reischer, R.J.; Ford, C.W.; Zurenko, G.E.; Hamel, J.C.; Schaadt, R.D.; Stapert, D.; Yagi, B.H. Substituent effects on the antibacterial activity of nitrogen-carbon-linked (azolylphenyl)oxazolidinones with expanded activity against the fastidious gram-negative organisms Haemophilus influenzae and Moraxella catarrhalis. J. Med. Chem. 2000, 43, 953-970.
-
-
-
-
8
-
-
0033623166
-
Human beta3-adrenergic receptor agonists containing 1,2,3-triazole-substituted benzenesulfonamides
-
Brockunier, L.L.; Parmee, E.R.; Ok, H.O.; Candelore, M.R.; Cascieri, M.A.; Colwell, L.F.; Deng, L.; Feeney, W.P.; Forrest, M.J.; Hom, G.J.; MacIntyre, D.E.; Tota, L.; Wyvratt, M.J.; Fisher, M. H.; Weber, A.E. Human beta3-adrenergic receptor agonists containing 1,2,3-triazole-substituted benzenesulfonamides. Bioorg. Med. Chem. Lett. 2000, 10, 2111-2114.
-
(2000)
Bioorg. Med. Chem. Lett
, vol.10
, pp. 2111-2114
-
-
Brockunier, L.L.1
Parmee, E.R.2
Ok, H.O.3
Candelore, M.R.4
Cascieri, M.A.5
Colwell, L.F.6
Deng, L.7
Feeney, W.P.8
Forrest, M.J.9
Hom, G.J.10
MacIntyre, D.E.11
Tota, L.12
Wyvratt, M.J.13
Fisher, M.H.14
Weber, A.E.15
-
9
-
-
26844454002
-
-
Pande, V.; Ramos, M.J. Structural basis for the GSK-3beta binding affinity and selectivity against CDK-2 of 1-(4-aminofurazan-3yl)-5- dialkylaminomethyl-1H-[1,2,3]triazole-4-carboxylic acid derivatives. Bioorg. Med. Chem. Lett. 2005, 15, 5129-5135.
-
Pande, V.; Ramos, M.J. Structural basis for the GSK-3beta binding affinity and selectivity against CDK-2 of 1-(4-aminofurazan-3yl)-5- dialkylaminomethyl-1H-[1,2,3]triazole-4-carboxylic acid derivatives. Bioorg. Med. Chem. Lett. 2005, 15, 5129-5135.
-
-
-
-
10
-
-
0037817456
-
-
Olesen, P.H.; Sørensen, A.R.; Ursö, B.; Kurtzhals, P.; Bowler, A.N.; Ehrbar, U.; Hansen, B.F. Synthesis and in vitro characterization of 1-(4-Aminofurazan-3-yl)-5-dialkylaminomethyl-1H-[1,2, 3]triazole-4-carboxylic acid derivatives. A new class of selective GSK-3 Inhibitors. J. Med. Chem. 2003, 46, 3333-3341.
-
Olesen, P.H.; Sørensen, A.R.; Ursö, B.; Kurtzhals, P.; Bowler, A.N.; Ehrbar, U.; Hansen, B.F. Synthesis and in vitro characterization of 1-(4-Aminofurazan-3-yl)-5-dialkylaminomethyl-1H-[1,2, 3]triazole-4-carboxylic acid derivatives. A new class of selective GSK-3 Inhibitors. J. Med. Chem. 2003, 46, 3333-3341.
-
-
-
-
11
-
-
18644384979
-
In situ selection of lead compounds by click chemistry: Target-guided optimization of aceylcholinesterase inhibitors
-
Krasinski, A.; Radic, Z.; Manetsch, R.; Raushel, J.; Taylor, P.; Sharpless, B.K.; Kolb, H.C. In situ selection of lead compounds by click chemistry: Target-guided optimization of aceylcholinesterase inhibitors. J. Am. Chem. Soc. 2005, 127, 6686-6692.
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 6686-6692
-
-
Krasinski, A.1
Radic, Z.2
Manetsch, R.3
Raushel, J.4
Taylor, P.5
Sharpless, B.K.6
Kolb, H.C.7
-
12
-
-
11244252206
-
In situ click chemistry: Enzyme-generated inhibitors of carbonic anhydrase II
-
Mocharla, V.P.; Colasson, B.; Lee, L.V.; Roeper, S.; Sharpless, B.K.; Wong, C.H.; Kolb, H.C. In situ click chemistry: Enzyme-generated inhibitors of carbonic anhydrase II. Angew. Chem. Int. Ed. 2005, 44, 116-120.
-
(2005)
Angew. Chem. Int. Ed
, vol.44
, pp. 116-120
-
-
Mocharla, V.P.1
Colasson, B.2
Lee, L.V.3
Roeper, S.4
Sharpless, B.K.5
Wong, C.H.6
Kolb, H.C.7
-
13
-
-
0023278943
-
Synthesis and. beta.-lactamase inhibitory properties of beta.-[(1,2,3-triazol-1-yl)methyl]-2. alpha.-methylpenam-3.alpha.-carboxylic acid 1,1-dioxide and related triazolyl derivatives
-
Micetich, R.G.; Maiti, S.N.; Spevak, P.; Hall, T.W.; Yamabe, S.; Ishida, N.; Tanaka, M.; Yamazaki, T.; Nakai, A.; Ogawa, K. Synthesis and. beta.-lactamase inhibitory properties of beta.-[(1,2,3-triazol-1-yl)methyl]-2. alpha.-methylpenam-3.alpha.-carboxylic acid 1,1-dioxide and related triazolyl derivatives. J. Med. Chem. 1987, 30, 1469-1474.
-
(1987)
J. Med. Chem
, vol.30
, pp. 1469-1474
-
-
Micetich, R.G.1
Maiti, S.N.2
Spevak, P.3
Hall, T.W.4
Yamabe, S.5
Ishida, N.6
Tanaka, M.7
Yamazaki, T.8
Nakai, A.9
Ogawa, K.10
-
14
-
-
0016769018
-
Laboratory studies with cefatrizine (SK + F 60771), a new broad-spectrum orally-active cephalosporin
-
Actor, P.; Uri, J.V.; Phillips, L.; Sachs, C.S.; Zajac, J.R.G.; Berges, D.A.; Dunn, G.L.; Hoover, J.R.E.; Weisbach, J.A. Laboratory studies with cefatrizine (SK + F 60771), a new broad-spectrum orally-active cephalosporin. J. Antibiot. 1975, 28, 594-601.
-
(1975)
J. Antibiot
, vol.28
, pp. 594-601
-
-
Actor, P.1
Uri, J.V.2
Phillips, L.3
Sachs, C.S.4
Zajac, J.R.G.5
Berges, D.A.6
Dunn, G.L.7
Hoover, J.R.E.8
Weisbach, J.A.9
-
15
-
-
0015523596
-
Broad-spectrum antiviral activity of Virazole: 1-Beta-D- ribofuranosyl-1,2,4-triazole-3-carboxamide
-
Sidwell, R.W.; Huffman, J.H.; Khare, G.P.; Allen, L.B.; Witkowski; J.T.; Robins, R.K. Broad-spectrum antiviral activity of Virazole: 1-Beta-D- ribofuranosyl-1,2,4-triazole-3-carboxamide. Science 1972, 177, 705-706.
-
(1972)
Science
, vol.177
, pp. 705-706
-
-
Sidwell, R.W.1
Huffman, J.H.2
Khare, G.P.3
Allen, L.B.4
Witkowski, J.T.5
Robins, R.K.6
-
16
-
-
0347129832
-
A highly potent non-nucleoside adenosine deaminase inhibitor: Efficient drug discovery by intentional lead hybridization
-
Terasaka, T.; Kinoshita, T.; Kuno, M.; Nakanishi, I. A highly potent non-nucleoside adenosine deaminase inhibitor: Efficient drug discovery by intentional lead hybridization, J. Am. Chem. Soc. 2004, 126, 34-35.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 34-35
-
-
Terasaka, T.1
Kinoshita, T.2
Kuno, M.3
Nakanishi, I.4
-
17
-
-
3142654156
-
Structure-based design, synthesis, and structure-activity relationship studies of novel non-nucleoside adenosine deaminase inhibitors
-
Terasaka, T.; Kinoshita, T.; Kuno, M.; Seki, N.; Tanaka, K.; Nakanishi, I. Structure-based design, synthesis, and structure-activity relationship studies of novel non-nucleoside adenosine deaminase inhibitors. J. Med. Chem. 2004, 47, 3730-3743.
-
(2004)
J. Med. Chem
, vol.47
, pp. 3730-3743
-
-
Terasaka, T.1
Kinoshita, T.2
Kuno, M.3
Seki, N.4
Tanaka, K.5
Nakanishi, I.6
-
18
-
-
2442670369
-
Structure-based design and synthesis of non-nucleoside, potent, and orally bioavailable adenosine deaminase inhibitors
-
Terasaka, T.; Okumura, H.; Tsuji, K.; Kato, T.; Nakanishi, I.; Kinoshita, T.; Kato, Y.; Kuno, M.; Seki, N.; Naoe, Y.; Inoue, T.; Tanaka, K.; Nakamura, K. Structure-based design and synthesis of non-nucleoside, potent, and orally bioavailable adenosine deaminase inhibitors. J. Med. Chem. 2004, 47, 2728-2731.
-
(2004)
J. Med. Chem
, vol.47
, pp. 2728-2731
-
-
Terasaka, T.1
Okumura, H.2
Tsuji, K.3
Kato, T.4
Nakanishi, I.5
Kinoshita, T.6
Kato, Y.7
Kuno, M.8
Seki, N.9
Naoe, Y.10
Inoue, T.11
Tanaka, K.12
Nakamura, K.13
-
19
-
-
22744453821
-
Rational design of non-nucleoside, potent, and orally bioavailable adenosine deaminase inhibitors: Predicting enzyme conformational change and metabolism
-
Terasaka, T.; Tsuji, K.; Kato, T.; Nakanishi, I.; Kinoshita, T.; Kato, Y.; Kuno, M.; Inoue, T.; Tanaka, K.; Nakamura, K. Rational design of non-nucleoside, potent, and orally bioavailable adenosine deaminase inhibitors: predicting enzyme conformational change and metabolism. J. Med. Chem. 2005, 48, 4750-4753.
-
(2005)
J. Med. Chem
, vol.48
, pp. 4750-4753
-
-
Terasaka, T.1
Tsuji, K.2
Kato, T.3
Nakanishi, I.4
Kinoshita, T.5
Kato, Y.6
Kuno, M.7
Inoue, T.8
Tanaka, K.9
Nakamura, K.10
-
20
-
-
4143116991
-
A structural basis for the inhibition of the NS5 dengue virus mRNA 2?-O-methyltransferase domain by ribavirin 5?-triphosphate
-
Benarroch, D.; Egloff, M.P.; Mulard, L.; Guerreiro, C.; Romette, J.L.; Canard, B. A structural basis for the inhibition of the NS5 dengue virus mRNA 2?-O-methyltransferase domain by ribavirin 5?-triphosphate. J. Biol. Chem. 2004, 279, 35638-35643.
-
(2004)
J. Biol. Chem
, vol.279
, pp. 35638-35643
-
-
Benarroch, D.1
Egloff, M.P.2
Mulard, L.3
Guerreiro, C.4
Romette, J.L.5
Canard, B.6
-
21
-
-
0037012920
-
-
Tornøe, C.; Christensen, C.; Meldal, M. Peptidotriazoles on solid phase: [1,2,3]-triazoles by regiospecific copper(I)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides. J. Org. Chem. 2002, 67, 3057-3064.
-
Tornøe, C.; Christensen, C.; Meldal, M. Peptidotriazoles on solid phase: [1,2,3]-triazoles by regiospecific copper(I)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides. J. Org. Chem. 2002, 67, 3057-3064.
-
-
-
-
22
-
-
0037099395
-
A stepwise huisgen cycloaddition process: Copper(I)-catalyzed regioselective ligation of azides and terminal alkynes
-
Rostovtsev, V.V.; Green, L.G.; Fokin, V.V.; Sharpless, B.K. A stepwise huisgen cycloaddition process: Copper(I)-catalyzed regioselective ligation of azides and terminal alkynes. Angew. Chem. Int. Ed. 2002, 41, 2596-2599.
-
(2002)
Angew. Chem. Int. Ed
, vol.41
, pp. 2596-2599
-
-
Rostovtsev, V.V.1
Green, L.G.2
Fokin, V.V.3
Sharpless, B.K.4
-
23
-
-
13444272999
-
Synthesis and biological testing of purine derivatives as potential ATP-competitive kinase inhibitors
-
Laufer, S.A.; Domeyer, D.M.; Scior, T.R.F.; Albrecht, W.; Hauser, D.R.J. Synthesis and biological testing of purine derivatives as potential ATP-competitive kinase inhibitors. J. Med. Chem. 2005, 48, 710-722.
-
(2005)
J. Med. Chem
, vol.48
, pp. 710-722
-
-
Laufer, S.A.1
Domeyer, D.M.2
Scior, T.R.F.3
Albrecht, W.4
Hauser, D.R.J.5
-
24
-
-
0000567032
-
Preparation of azido derivatives from amino acids and peptides by diazo transfer
-
Zaloom, J.; Roberts, D.C. Preparation of azido derivatives from amino acids and peptides by diazo transfer. J. Org. Chem. 1981, 46, 5173-5176.
-
(1981)
J. Org. Chem
, vol.46
, pp. 5173-5176
-
-
Zaloom, J.1
Roberts, D.C.2
-
25
-
-
84987493202
-
Convenient synthesis of 2-Azido-2-deoxy-aldoses by diazo transfer
-
Vasella, A.; Witzig, C.; Chiara, J.L.; Lomas, M.M. Convenient synthesis of 2-Azido-2-deoxy-aldoses by diazo transfer. Helv. Chim. Acta 1991, 74, 2073-2077.
-
(1991)
Helv. Chim. Acta
, vol.74
, pp. 2073-2077
-
-
Vasella, A.1
Witzig, C.2
Chiara, J.L.3
Lomas, M.M.4
-
27
-
-
0037030609
-
Conformations and receptor activity of desmopressin analogues, which contain gamma-turn mimetics or a psi[CH(2)O] isostere
-
Hedenström, M.; Yuan, Z.; Brickmann, K.; Carlsson, J.; Ekholm, K.; Johansson, B.; Kreutz, E.; Nilsson, A.; Sethson, I.; Kihlberg, J. Conformations and receptor activity of desmopressin analogues, which contain gamma-turn mimetics or a psi[CH(2)O] isostere. J. Med. Chem. 2002, 45, 2501-2511.
-
(2002)
J. Med. Chem
, vol.45
, pp. 2501-2511
-
-
Hedenström, M.1
Yuan, Z.2
Brickmann, K.3
Carlsson, J.4
Ekholm, K.5
Johansson, B.6
Kreutz, E.7
Nilsson, A.8
Sethson, I.9
Kihlberg, J.10
-
28
-
-
18244376860
-
Modular synthesis of cyclic peptidomimetics inspired by γ-turns
-
Ramanathan, S.K.; Keeler, J.; Lee, H.L.; Reddy, D.S.; Lushington, G.; Aube, J. Modular synthesis of cyclic peptidomimetics inspired by γ-turns. Org. Lett. 2005, 7, 1059-1062.
-
(2005)
Org. Lett
, vol.7
, pp. 1059-1062
-
-
Ramanathan, S.K.1
Keeler, J.2
Lee, H.L.3
Reddy, D.S.4
Lushington, G.5
Aube, J.6
-
29
-
-
33646798112
-
Synthesis of 1,4,5-trisubstituted-1,2,3-triazoles by copper-catalyzed cycloaddition-coupling of azides and terminal
-
Gerard, B.; Ryan, J.; Beeler, A.B.; Porco, J.A., Jr. Synthesis of 1,4,5-trisubstituted-1,2,3-triazoles by copper-catalyzed cycloaddition-coupling of azides and terminal. Tetrahedron 2006, 62, 6405-6411.
-
(2006)
Tetrahedron
, vol.62
, pp. 6405-6411
-
-
Gerard, B.1
Ryan, J.2
Beeler, A.B.3
Porco Jr., J.A.4
-
30
-
-
0037454346
-
-
Wang, Q.; Chan, T.R.; Hilgraf, R.; Fokin, V.V.; Sharpless, B.K.; Finn, M.G. Bioconjugation by copper(I)-catalyzed azide-alkyne [3+2] cycloaddition. J. Am. Chem. Soc. 2003, 125, 3192-3193.
-
Wang, Q.; Chan, T.R.; Hilgraf, R.; Fokin, V.V.; Sharpless, B.K.; Finn, M.G. Bioconjugation by copper(I)-catalyzed azide-alkyne [3+2] cycloaddition. J. Am. Chem. Soc. 2003, 125, 3192-3193.
-
-
-
-
31
-
-
11844255741
-
Copper(I)-catalyzed synthesis of azoles. DFT study predicts unprecedented reactivity and intermediates
-
Himo, F.; Lovell, T.; Hilgraf, R.; Rostovtsev, V.V.; Noodleman, L.; Sharpless, B.K.; Fokin, V.V. Copper(I)-catalyzed synthesis of azoles. DFT study predicts unprecedented reactivity and intermediates. J. Am. Chem. Soc. 2005, 127, 210-216.
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 210-216
-
-
Himo, F.1
Lovell, T.2
Hilgraf, R.3
Rostovtsev, V.V.4
Noodleman, L.5
Sharpless, B.K.6
Fokin, V.V.7
-
32
-
-
4444324951
-
Polytriazoles as copper(I)-stabilizing ligands in catalysis
-
Chan, T.R.; Hilgraf, R.; Sharpless; B.K.; Fokin, V.V. Polytriazoles as copper(I)-stabilizing ligands in catalysis. Org. Lett. 2004, 6, 2853-2855.
-
(2004)
Org. Lett
, vol.6
, pp. 2853-2855
-
-
Chan, T.R.1
Hilgraf, R.2
Sharpless, B.K.3
Fokin, V.V.4
-
33
-
-
0038669312
-
An efficient strategy for the synthesis of chiral liquid crystals using Evans' methodology
-
Merlo, A.A.; Fernandes, M.S. An efficient strategy for the synthesis of chiral liquid crystals using Evans' methodology. Synth. Commun. 2003, 33, 1167-1178.
-
(2003)
Synth. Commun
, vol.33
, pp. 1167-1178
-
-
Merlo, A.A.1
Fernandes, M.S.2
-
34
-
-
0037428017
-
Novel stereoselective synthesis of functionalized oxazolidinones from chiral aziridines
-
Park, C.S.; Kim, M.S.; Sim, T.B.; Pyun, D.K.; Lee, C.H.; Choi, D.; Lee, W.K.; Chang, J.W.; Ha, H.J. Novel stereoselective synthesis of functionalized oxazolidinones from chiral aziridines. J. Org. Chem. 2003, 68, 43-49.
-
(2003)
J. Org. Chem
, vol.68
, pp. 43-49
-
-
Park, C.S.1
Kim, M.S.2
Sim, T.B.3
Pyun, D.K.4
Lee, C.H.5
Choi, D.6
Lee, W.K.7
Chang, J.W.8
Ha, H.J.9
-
35
-
-
0001474852
-
Synthesis, regioselective deprotonation, and stereoselective alkylation of fluoro ketimines
-
Welch J.T.; Seper, K.W. Synthesis, regioselective deprotonation, and stereoselective alkylation of fluoro ketimines. J. Org. Chem. 1988, 53, 2991-2999.
-
(1988)
J. Org. Chem
, vol.53
, pp. 2991-2999
-
-
Welch, J.T.1
Seper, K.W.2
-
36
-
-
84985258717
-
Synthese diastereomerenreiner 2,5-disubstituierter 3-Oxoperhydro-1,4-oxazine
-
Danklmaier, J.; Hoenig, H. Synthese diastereomerenreiner 2,5-disubstituierter 3-Oxoperhydro-1,4-oxazine. Liebigs Ann. Chem. 1988, 851-854.
-
(1988)
Liebigs Ann. Chem
, pp. 851-854
-
-
Danklmaier, J.1
Hoenig, H.2
-
39
-
-
33750124980
-
Extra precision glide: Docking and scoring incorporating a model of hydrophobic enclosure for protein-ligand complexes
-
Friesner, R.A.; Murphy, R.B.; Repasky, M.P.; Frye, L.L.; Greenwood, J.R.; Halgren, T.A.; Sanschagrin, P.C.; Mainz, D.T. Extra precision glide: Docking and scoring incorporating a model of hydrophobic enclosure for protein-ligand complexes. J. Med. Chem. 2006, 49, 6196.
-
(2006)
J. Med. Chem
, vol.49
, pp. 6196
-
-
Friesner, R.A.1
Murphy, R.B.2
Repasky, M.P.3
Frye, L.L.4
Greenwood, J.R.5
Halgren, T.A.6
Sanschagrin, P.C.7
Mainz, D.T.8
|