-
2
-
-
33947572059
-
Thioureas
-
1:CAS:528:DyaG2MXjt1Wnug%3D%3D 10.1021/cr50001a005
-
D.C. Schroeder 1955 Thioureas Chem Rev 55 181 228 1:CAS:528: DyaG2MXjt1Wnug%3D%3D 10.1021/cr50001a005
-
(1955)
Chem Rev
, vol.55
, pp. 181-228
-
-
Schroeder, D.C.1
-
3
-
-
0032287025
-
Synthesis, hypotensive and antiarrhythmic activities of 3-alkyl-1-(2-hydroxy-5,8-dimethoxy-1,2,3,4-tetrahydro-3-naphthalenyl)ureas or thioureas and their guanidine analogues
-
1:CAS:528:DyaK1MXoslOluw%3D%3D 10.1016/S0223-5234(99)80022-1
-
E.G. Chalina L. Chakarova 1998 Synthesis, hypotensive and antiarrhythmic activities of 3-alkyl-1-(2-hydroxy-5,8-dimethoxy-1,2,3,4-tetrahydro-3- naphthalenyl)ureas or thioureas and their guanidine analogues Eur J Med Chem 33 975 983 1:CAS:528:DyaK1MXoslOluw%3D%3D 10.1016/S0223-5234(99)80022-1
-
(1998)
Eur J Med Chem
, vol.33
, pp. 975-983
-
-
Chalina, E.G.1
Chakarova, L.2
-
4
-
-
0029877782
-
Novel carbamates as potent histamine H3 receptor antagonists with high in vitro and oral in vivo activity
-
1:CAS:528:DyaK28XpsFKgtA%3D%3D 10.1021/jm9507688
-
H. Stark K. Purand X. Ligneau A. Rouleau J.M. Arrang M. Garbarg J.C. Schwartz W. Schunack 1996 Novel carbamates as potent histamine H3 receptor antagonists with high in vitro and oral in vivo activity J Med Chem 39 1157 1163 1:CAS:528:DyaK28XpsFKgtA%3D%3D 10.1021/jm9507688
-
(1996)
J Med Chem
, vol.39
, pp. 1157-1163
-
-
Stark, H.1
Purand, K.2
Ligneau, X.3
Rouleau, A.4
Arrang, J.M.5
Garbarg, M.6
Schwartz, J.C.7
Schunack, W.8
-
5
-
-
15644373566
-
2-Nitrophenylcarbamoyl-(S)-prolyl-(S)-3-(2-naphthyl)alanyl-N-benzy l-N-methylamide (SDZ NKT 343), a potent human NK1 tachykinin receptor antagonist with good oral analgesic activity in chronic pain models
-
1:CAS:528:DyaK1cXltVGnurs%3D 10.1021/jm970499g
-
C. Walpole S.Y. Ko M. Brown D. Beattie E. Campbell F. Dickenson S. Ewan G.A. Hughes M. Lemaire J. Lerpiniere S. Patel L. Urban 1998 2- Nitrophenylcarbamoyl-(S)-prolyl-(S)-3-(2-naphthyl)alanyl-N-benzy l-N-methylamide (SDZ NKT 343), a potent human NK1 tachykinin receptor antagonist with good oral analgesic activity in chronic pain models J Med Chem 41 3159 3173 1:CAS:528:DyaK1cXltVGnurs%3D 10.1021/jm970499g
-
(1998)
J Med Chem
, vol.41
, pp. 3159-3173
-
-
Walpole, C.1
Ko, S.Y.2
Brown, M.3
Beattie, D.4
Campbell, E.5
Dickenson, F.6
Ewan, S.7
Hughes, G.A.8
Lemaire, M.9
Lerpiniere, J.10
Patel, S.11
Urban, L.12
-
6
-
-
0037165402
-
H-bonding additives act like Lewis acid catalysts
-
1:CAS:528:DC%2BD38XhsVWktA%3D%3D 10.1021/ol017117s
-
P.R. Schreiner A. Wittkopp 2002 H-bonding additives act like Lewis acid catalysts Org Lett 4 217 220 1:CAS:528:DC%2BD38XhsVWktA%3D%3D 10.1021/ol017117s
-
(2002)
Org Lett
, vol.4
, pp. 217-220
-
-
Schreiner, P.R.1
Wittkopp, A.2
-
7
-
-
0037455338
-
Metal-free, noncovalent catalysis of Diels-Alder reactions by neutral hydrogen bond donors in organic solvents and in water
-
1:CAS:528:DC%2BD3sXnvFCrsg%3D%3D 10.1002/chem.200390042
-
A. Wittkopp P.R. Schreiner 2003 Metal-free, noncovalent catalysis of Diels-Alder reactions by neutral hydrogen bond donors in organic solvents and in water Chem Eur J 9 407 414 1:CAS:528:DC%2BD3sXnvFCrsg%3D%3D 10.1002/chem.200390042
-
(2003)
Chem Eur J
, vol.9
, pp. 407-414
-
-
Wittkopp, A.1
Schreiner, P.R.2
-
8
-
-
33746277515
-
Organocatalysis mediated by (thio)urea derivatives
-
10.1002/chem.200501076
-
S.J. Connon 2006 Organocatalysis mediated by (thio)urea derivatives Chem Eur J 12 5418 5427 10.1002/chem.200501076
-
(2006)
Chem Eur J
, vol.12
, pp. 5418-5427
-
-
Connon, S.J.1
-
9
-
-
34548305129
-
Organocatalytic biomimetic reduction of conjugated nitroalkenes
-
Z. Zhang P.R. Schreiner 2007 Organocatalytic biomimetic reduction of conjugated nitroalkenes Synthesis 16 2559 2564
-
(2007)
Synthesis
, vol.16
, pp. 2559-2564
-
-
Zhang, Z.1
Schreiner, P.R.2
-
10
-
-
0033818253
-
Stereochemistry of halopyridyl and thiazolyl thiourea compounds is a major determinant of their potency as nonnucleoside inhibitors of HIV-1 reverse transcriptase
-
1:CAS:528:DC%2BD3cXmtF2htro%3D 10.1016/S0960-894X(00)00398-X
-
T.K. Venkatachalam E.A. Sudbeck C. Mao F.M. Uckun 2000 Stereochemistry of halopyridyl and thiazolyl thiourea compounds is a major determinant of their potency as nonnucleoside inhibitors of HIV-1 reverse transcriptase Bioorg Med Chem Lett 10 2071 2074 1:CAS:528:DC%2BD3cXmtF2htro%3D 10.1016/S0960-894X(00) 00398-X
-
(2000)
Bioorg Med Chem Lett
, vol.10
, pp. 2071-2074
-
-
Venkatachalam, T.K.1
Sudbeck, E.A.2
Mao, C.3
Uckun, F.M.4
-
11
-
-
0035952259
-
Anti-HIV activity of aromatic and heterocyclic thiazolyl thiourea compounds
-
1:CAS:528:DC%2BD3MXhslOnsrk%3D 10.1016/S0960-894X(01)00011-7
-
T.K. Venkatachalam E.A. Sudbeck C. Mao F.M. Uckun 2001 Anti-HIV activity of aromatic and heterocyclic thiazolyl thiourea compounds Bioorg Med Chem Lett 11 523 528 1:CAS:528:DC%2BD3MXhslOnsrk%3D 10.1016/S0960-894X(01)00011-7
-
(2001)
Bioorg Med Chem Lett
, vol.11
, pp. 523-528
-
-
Venkatachalam, T.K.1
Sudbeck, E.A.2
Mao, C.3
Uckun, F.M.4
-
12
-
-
0035197888
-
Stereochemistry as a major determinant of the anti-HIV activity of chiral naphthyl thiourea compounds
-
1:CAS:528:DC%2BD3MXptVKmu7c%3D
-
T.K. Venkatachalam C. Mao F.M. Uckun 2001 Stereochemistry as a major determinant of the anti-HIV activity of chiral naphthyl thiourea compounds Antiviral Chem & Chemother 12 213 221 1:CAS:528:DC%2BD3MXptVKmu7c%3D
-
(2001)
Antiviral Chem & Chemother
, vol.12
, pp. 213-221
-
-
Venkatachalam, T.K.1
Mao, C.2
Uckun, F.M.3
-
13
-
-
2342502598
-
Effect of stereo and regiochemistry towards wild and multidrug resistant HIV-1 virus: Viral potency of chiral PETT derivatives
-
1:CAS:528:DC%2BD2cXjvVCju70%3D 10.1016/j.bcp.2004.01.019
-
T.K. Venkatachalam C. Mao F.A. Uckun 2004 Effect of stereo and regiochemistry towards wild and multidrug resistant HIV-1 virus: Viral potency of chiral PETT derivatives Biochem Pharmaco 67 1933 1946 1:CAS:528: DC%2BD2cXjvVCju70%3D 10.1016/j.bcp.2004.01.019
-
(2004)
Biochem Pharmaco
, vol.67
, pp. 1933-1946
-
-
Venkatachalam, T.K.1
Mao, C.2
Uckun, F.A.3
-
14
-
-
3042836102
-
Effect of stereochemistry on the anti-HIV activity of chiral thiourea compounds
-
1:CAS:528:DC%2BD2cXls1Wnuro%3D 10.1016/j.bmc.2004.04.050
-
T.K. Venkatachalam C. Mao F.M. Uckun 2004 Effect of stereochemistry on the anti-HIV activity of chiral thiourea compounds Bioorg Med Chem 12 4275 4284 1:CAS:528:DC%2BD2cXls1Wnuro%3D 10.1016/j.bmc.2004.04.050
-
(2004)
Bioorg Med Chem
, vol.12
, pp. 4275-4284
-
-
Venkatachalam, T.K.1
Mao, C.2
Uckun, F.M.3
-
15
-
-
84913150907
-
Biological activity of aminophosphonic acids
-
Kafarski P; Lejczak B. Biological activity of aminophosphonic acids. Phosphorus Sulfur 1991, 63, 193-215
-
(1991)
Phosphorus Sulfur
, vol.63
, pp. 193-215
-
-
Kafarski, P.1
Lejczak, B.2
-
16
-
-
3342968602
-
Synthesis and bioactivity of α-aminophosphonates containing fluorine
-
1:CAS:528:DC%2BD3sXjtFymurw%3D 10.3390/80100186
-
B.A. Song Y.L. Wu S. Yang D.Y. Hu X.Q. He L.H. Jin P. Lu 2003 Synthesis and bioactivity of α-aminophosphonates containing fluorine Molecules 8 186 192 1:CAS:528:DC%2BD3sXjtFymurw%3D 10.3390/80100186
-
(2003)
Molecules
, vol.8
, pp. 186-192
-
-
Song, B.A.1
Wu, Y.L.2
Yang, S.3
Hu, D.Y.4
He, X.Q.5
Jin, L.H.6
Lu, P.7
-
17
-
-
33750963441
-
Synthesis and antifungal activity of novel chiral R-aminophosphonates containing fluorine moiety
-
1:CAS:528:DC%2BD28Xht1aksLjE 10.1002/cjoc.200690296
-
S. Yang X.W. Gao C.L. Diao B.A. Song L.H. Jin G.F. Xu G.P. Zhang W. Wang D.Y. Hu W. Xue X. Zhou P. Lu 2006 Synthesis and antifungal activity of novel chiral R-aminophosphonates containing fluorine moiety Chin J Chem 24 1581 1588 1:CAS:528:DC%2BD28Xht1aksLjE 10.1002/cjoc.200690296
-
(2006)
Chin J Chem
, vol.24
, pp. 1581-1588
-
-
Yang, S.1
Gao, X.W.2
Diao, C.L.3
Song, B.A.4
Jin, L.H.5
Xu, G.F.6
Zhang, G.P.7
Wang, W.8
Hu, D.Y.9
Xue, W.10
Zhou, X.11
Lu, P.12
-
18
-
-
33751154738
-
Catalytic asymmetric synthesis of α-amino phosphonates using Lanthanoid-Potassium-BINOL complexes
-
1:CAS:528:DyaK2MXotleltbg%3D 10.1021/jo00126a003
-
H. Sasai S. Arai Y. Tahara 1995 Catalytic asymmetric synthesis of α-amino phosphonates using Lanthanoid-Potassium-BINOL complexes J Org Chem 60 6656 6657 1:CAS:528:DyaK2MXotleltbg%3D 10.1021/jo00126a003
-
(1995)
J Org Chem
, vol.60
, pp. 6656-6657
-
-
Sasai, H.1
Arai, S.2
Tahara, Y.3
-
19
-
-
8744256339
-
Metal triflate-catalyzed one-pot synthesis of a-aminophosphonates from carbonyl compounds in the absence of solvent
-
10.1055/s-2004-831251
-
H. Firouzabadi N. Iranpoor S.I. Sobhan 2004 Metal triflate-catalyzed one-pot synthesis of a-aminophosphonates from carbonyl compounds in the absence of solvent Synthesis 16 2692 10.1055/s-2004-831251
-
(2004)
Synthesis
, vol.16
, pp. 2692
-
-
Firouzabadi, H.1
Iranpoor, N.2
Sobhan, S.I.3
-
20
-
-
0042431530
-
One-pot synthesis of α-aminophosphonates: An inexpensive approach
-
1:CAS:528:DC%2BD3sXmvFCns7c%3D 10.1081/SCC-120022468
-
A. Manjula B.R. Vittal P. Neelakantan 2003 One-pot synthesis of α-aminophosphonates: An inexpensive approach Synth Commun 33 2963 2969 1:CAS:528:DC%2BD3sXmvFCns7c%3D 10.1081/SCC-120022468
-
(2003)
Synth Commun
, vol.33
, pp. 2963-2969
-
-
Manjula, A.1
Vittal, B.R.2
Neelakantan, P.3
-
21
-
-
0037467898
-
A convenient synthesis of 1-aminophosphonates from 1-hydroxyphosphonates
-
1:CAS:528:DC%2BD3sXhtFCnurc%3D 10.1016/S0040-4039(02)02727-2
-
B. Kaboudin 2003 A convenient synthesis of 1-aminophosphonates from 1-hydroxyphosphonates Tetrahedron Lett 44 1051 1053 1:CAS:528: DC%2BD3sXhtFCnurc%3D 10.1016/S0040-4039(02)02727-2
-
(2003)
Tetrahedron Lett
, vol.44
, pp. 1051-1053
-
-
Kaboudin, B.1
-
22
-
-
0036924494
-
A simple and green procedure for the synthesis of α- aminophosphonate by a one-pot three-component condensation of carbonyl compound, amine and diethyl phosphite without solvent and catalyst
-
1:CAS:528:DC%2BD38Xpt1Citbs%3D 10.1039/b205747f
-
B.C. Ranu R.A. Hajra 2002 A simple and green procedure for the synthesis of α-aminophosphonate by a one-pot three-component condensation of carbonyl compound, amine and diethyl phosphite without solvent and catalyst Green Chem 4 551 554 1:CAS:528:DC%2BD38Xpt1Citbs%3D 10.1039/b205747f
-
(2002)
Green Chem
, vol.4
, pp. 551-554
-
-
Ranu, B.C.1
Hajra, R.A.2
-
23
-
-
64549109038
-
Synthesis and antiviral activities of chiral thiourea derivatives containing an α-aminophosphonate moiety
-
1:CAS:528:DC%2BD1MXpsl2jsA%3D%3D 10.1021/jf803215t
-
M.H. Chen Z. Chen B.A. Song P.S. Bhadury S. Yang X.J. Cai D.Y. Hu W. Xue S. Zheng 2009 Synthesis and antiviral activities of chiral thiourea derivatives containing an α-aminophosphonate moiety J Agric Food Chem 57 1383 1388 1:CAS:528:DC%2BD1MXpsl2jsA%3D%3D 10.1021/jf803215t
-
(2009)
J Agric Food Chem
, vol.57
, pp. 1383-1388
-
-
Chen, M.H.1
Chen, Z.2
Song, B.A.3
Bhadury, P.S.4
Yang, S.5
Cai, X.J.6
Hu, D.Y.7
Xue, W.8
Zheng, S.9
-
24
-
-
33947668980
-
Reductase-mimicking thiourea organocatalyst incorporating a covalently bound NADH analogue: Efficient 1,2-diketone reduction with in situ prosthetic group generation and recycling
-
10.1039/b618792g
-
B. Procuranti S.J.A. Connon 2007 Reductase-mimicking thiourea organocatalyst incorporating a covalently bound NADH analogue: Efficient 1,2-diketone reduction with in situ prosthetic group generation and recycling Chem Commun 14 1421 1423 10.1039/b618792g
-
(2007)
Chem Commun
, vol.14
, pp. 1421-1423
-
-
Procuranti, B.1
Connon, S.J.A.2
-
25
-
-
15944409935
-
A simple and convenient procedure for the synthesis of 1-aminophosphonates from aromatic aldehydes
-
1:CAS:528:DC%2BD2MXivVKhu7k%3D 10.1016/j.tetlet.2005.03.037
-
B. Kaboudin K. Moradi 2005 A simple and convenient procedure for the synthesis of 1-aminophosphonates from aromatic aldehydes Tetrahedron Lett. 46 2989 2991 1:CAS:528:DC%2BD2MXivVKhu7k%3D 10.1016/j.tetlet.2005.03.037
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 2989-2991
-
-
Kaboudin, B.1
Moradi, K.2
-
26
-
-
64549156959
-
Preparation of isocyanates, isothiocyanates and isoselenocyanates in the laboratory
-
1:CAS:528:DC%2BD38XmvFWkur4%3D
-
T. Wang W.F. Ye H.W. He 2002 Preparation of isocyanates, isothiocyanates and isoselenocyanates in the laboratory Chem Reagent 24 4 204 207 1:CAS:528:DC%2BD38XmvFWkur4%3D
-
(2002)
Chem Reagent
, vol.24
, Issue.4
, pp. 204-207
-
-
Wang, T.1
Ye, W.F.2
He, H.W.3
-
27
-
-
0014152185
-
A simple technique for purification of tobacco mosaic virus in large quantities
-
G.V. Gooding Jr T.T. Hebert 1967 A simple technique for purification of tobacco mosaic virus in large quantities Phytopathology. 57 1285 1290
-
(1967)
Phytopathology.
, vol.57
, pp. 1285-1290
-
-
Gooding Jr., G.V.1
Hebert, T.T.2
-
28
-
-
27144449016
-
Synthesis and antiviral activity of novel chiral cyanoacrylate derivatives
-
1:CAS:528:DC%2BD2MXpslCitLk%3D 10.1021/jf051050w
-
B.A. Song H.P. Zhang H. Wang S. Yang L.H. Jin D.Y. Hu L.L. Pang W. Xue 2005 Synthesis and antiviral activity of novel chiral cyanoacrylate derivatives J Agric Food Chem 53 7886 7891 1:CAS:528:DC%2BD2MXpslCitLk%3D 10.1021/jf051050w
-
(2005)
J Agric Food Chem
, vol.53
, pp. 7886-7891
-
-
Song, B.A.1
Zhang, H.P.2
Wang, H.3
Yang, S.4
Jin, L.H.5
Hu, D.Y.6
Pang, L.L.7
Xue, W.8
|