-
1
-
-
38949083855
-
The chemical versatility of natural-product assembly lines
-
Walsh, C.T. The chemical versatility of natural-product assembly lines. Acc. Chem. Res. 2008, 41, 4-10.
-
(2008)
Acc. Chem. Res.
, vol.41
, pp. 4-10
-
-
Walsh, C.T.1
-
2
-
-
32344434405
-
Natural products from marine organisms and their associated microbes
-
König, G.M.; Kehraus, S.; Seibert, S.F.; Abdel-Lateff, A.; Müller, D. Natural products from marine organisms and their associated microbes. ChemBioChem 2006, 7, 229-238.
-
(2006)
ChemBioChem
, vol.7
, pp. 229-238
-
-
König, G.M.1
Kehraus, S.2
Seibert, S.F.3
Abdel-Lateff, A.4
Müller, D.5
-
3
-
-
34249797901
-
Biomedicinals from the phytosymbionts of marine invertebrates: A molecular approach
-
Dunlap, W.C.; Battershill, C.N.; Liptrot, C.H.; Cobb, R.E.; Bourne, D.G.; Jaspars, M.; Long, P.F.; Newman, D.J. Biomedicinals from the phytosymbionts of marine invertebrates: A molecular approach. Methods 2007, 42, 358-376.
-
(2007)
Methods
, vol.42
, pp. 358-376
-
-
Dunlap, W.C.1
Battershill, C.N.2
Liptrot, C.H.3
Cobb, R.E.4
Bourne, D.G.5
Jaspars, M.6
Long, P.F.7
Newman, D.J.8
-
4
-
-
33645329115
-
Plant cyclopeptides
-
Tan, N.-H.; Zhou, J. Plant cyclopeptides. Chem. Rev. 2006, 106, 840-895.
-
(2006)
Chem. Rev.
, vol.106
, pp. 840-895
-
-
Tan, N.-H.1
Zhou, J.2
-
5
-
-
0018770021
-
Highly active cyclic and bicyclic somatostatin analogues of reduced ring size
-
Veber, D.F.; Holly, F.W.; Nutt, R.F.; Bergstrand, S.J.; Brady, S.F.; Hirschmann, R.; Glitzer, M.S.; Saperstein, R. Highly active cyclic and bicyclic somatostatin analogues of reduced ring size. Nature 1979, 280, 512-514.
-
(1979)
Nature
, vol.280
, pp. 512-514
-
-
Veber, D.F.1
Holly, F.W.2
Nutt, R.F.3
Bergstrand, S.J.4
Brady, S.F.5
Hirschmann, R.6
Glitzer, M.S.7
Saperstein, R.8
-
6
-
-
0019862208
-
A potent cyclic hexapeptide analogue of somatostatin
-
Veber, D.F.; Freidlinger, R.M.; Perlow, D.S.; Paleveda, W.J., Jr.; Holly, F.W.; Stachan, R.G.; Nutt, R.F.; Arison, B.H.; Homnick, C.; Randall, W.C.; et al. A potent cyclic hexapeptide analogue of somatostatin. Nature 1981, 292, 55-58.
-
(1981)
Nature
, vol.292
, pp. 55-58
-
-
Veber, D.F.1
Freidlinger, R.M.2
Perlow, D.S.3
Paleveda Jr., W.J.4
Holly, F.W.5
Stachan, R.G.6
Nutt, R.F.7
Arison, B.H.8
Homnick, C.9
Randall, W.C.10
-
7
-
-
44949231073
-
Peptidomimetics a synthetic tool of drug discovery
-
Vagner, J.; Qu, H.; Hruby, V.J. Peptidomimetics, a synthetic tool of drug discovery. Curr. Opin. Chem. Biol. 2008, 12, 292-296.
-
(2008)
Curr. Opin. Chem. Biol.
, vol.12
, pp. 292-296
-
-
Vagner, J.1
Qu, H.2
Hruby, V.J.3
-
8
-
-
0043245859
-
Peptides with anticancer use or potential
-
Janin, Y.L. Peptides with anticancer use or potential. Amino Acids 2003, 25, 1-40.
-
(2003)
Amino Acids
, vol.25
, pp. 1-40
-
-
Janin, Y.L.1
-
9
-
-
0037332151
-
Bistratamides e-j modified cyclic hexapeptides from the philippines ascidian lissoclinum bistratum
-
Perez, L.J.; Faulkner, D.J. Bistratamides E-J, modified cyclic hexapeptides from the Philippines ascidian Lissoclinum bistratum. J. Nat. Prod. 2003, 66, 247-250.
-
(2003)
J. Nat. Prod.
, vol.66
, pp. 247-250
-
-
Perez, L.J.1
Faulkner, D.J.2
-
10
-
-
35648951171
-
From amino acids to heteroaromatics-thiopeptide antibiotics, nature's heterocyclic peptides
-
Hughes, R.A.; Moody, C.J. From amino acids to heteroaromatics-Thiopeptide antibiotics, nature's heterocyclic peptides. Angew. Chem. Int. Ed. Engl. 2007, 46, 7930-7954.
-
(2007)
Angew. Chem. Int. Ed. Engl.
, vol.46
, pp. 7930-7954
-
-
Hughes, R.A.1
Moody, C.J.2
-
11
-
-
0042659297
-
Concise synthesis of stereodefined, thiazole-containing cyclic hexa- and octapeptide relatives of the lissoclinums, via cyclooligomerisation reactions
-
Bertram, A.; Blake, A.J.; de Turiso, F.G.-L.; Hannam, J.S.; Jolliffe, K.A.; Pattenden, G.; Skae, M. Concise synthesis of stereodefined, thiazole-containing cyclic hexa- and octapeptide relatives of the Lissoclinums, via cyclooligomerisation reactions. Tetrahedron 2003, 59, 6979-6990.
-
(2003)
Tetrahedron
, vol.59
, pp. 6979-6990
-
-
Bertram, A.1
Blake, A.J.2
De Turiso, F.G.-L.3
Hannam, J.S.4
Jolliffe, K.A.5
Pattenden, G.6
Skae, M.7
-
12
-
-
34250715957
-
Synthesis of libraries of thiazole, oxazole, and imidazole-based cyclic peptides from azole-based amino acids. A new synthetic approach to bistratamides and didmolamides
-
Bertram, A.; Maulucci, N.; New, O.M.; Nor, S.M.M.; Pattenden, G. Synthesis of libraries of thiazole, oxazole, and imidazole-based cyclic peptides from azole-based amino acids. A new synthetic approach to Bistratamides and Didmolamides. Org. Biomol. Chem. 2007, 5, 1541-1553.
-
(2007)
Org. Biomol. Chem.
, vol.5
, pp. 1541-1553
-
-
Bertram, A.1
Maulucci, N.2
New, O.M.3
Nor, S.M.M.4
Pattenden, G.5
-
13
-
-
38349048323
-
Structural investigation of westiellamide analogues
-
Haberhauer, G.; Drosdow, E.; Oeser, T.; Rominger, F. Structural investigation of Westiellamide analogues. Tetrahedron 2008, 64, 1853-1859.
-
(2008)
Tetrahedron
, vol.64
, pp. 1853-1859
-
-
Haberhauer, G.1
Drosdow, E.2
Oeser, T.3
Rominger, F.4
-
14
-
-
46049100010
-
Total synthesis and molecular target of largazole, a histone deacetylase inhibitor
-
Ying, Y.; Taori, K.; Kim, H.; Hong, J.; Luesch, H. Total synthesis and molecular target of Largazole, a histone deacetylase inhibitor. J. Am. Chem. Soc. 2008, 130, 8455-8459.
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 8455-8459
-
-
Ying, Y.1
Taori, K.2
Kim, H.3
Hong, J.4
Luesch, H.5
-
15
-
-
0347719294
-
Highly efficient biomimetic total synthesis and structural verification of bistratamides e and j from lissoclinum bistratum
-
You, S.-L.; Kelly, J.W. Highly efficient biomimetic total synthesis and structural verification of Bistratamides E and J from Lissoclinum bistratum. Chem. Eur. J. 2004, 10, 71-75.
-
(2004)
Chem. Eur. J.
, vol.10
, pp. 71-75
-
-
You, S.-L.1
Kelly, J.W.2
-
16
-
-
4043055319
-
Solid-phase synthesis and stereochemical assignments of tenuecyclamides a-d employing heterocyclic amino acids derived from commercially available fmoc a-amino acids
-
You, S.-L.; Deechongkit, S.; Kelly, J.W. Solid-phase synthesis and stereochemical assignments of Tenuecyclamides A-D employing heterocyclic amino acids derived from commercially available Fmoc a-amino acids. Org. Lett. 2004, 6, 2627-2630.
-
(2004)
Org. Lett.
, vol.6
, pp. 2627-2630
-
-
You, S.-L.1
Deechongkit, S.2
Kelly, J.W.3
-
17
-
-
3042558153
-
Synthesis and investigation of a new cyclo(na-dipicolinyl)pentapeptide of a breast and cns cytotoxic activity and an ionophoric specificity
-
Abo-Ghalia, M.; Amr, A. Synthesis and investigation of a new cyclo(Na-dipicolinyl)pentapeptide of a breast and CNS cytotoxic activity and an ionophoric specificity. Amino Acids 2004, 26, 283-289.
-
(2004)
Amino Acids
, vol.26
, pp. 283-289
-
-
Abo-Ghalia, M.1
Amr, A.2
-
18
-
-
53849131677
-
Backbone amide linker strategy for the synthesis of 1,4-triazole- containing cyclic tetra- and pentapeptides
-
Springer, J.; de Cuba, K.R.; Calvet-Vitale, S.; Geenevasen, J.A.J.; Hermkens, P.H.H.; Hiemstra, H.; van Maarseveen, J.H. Backbone amide linker strategy for the synthesis of 1,4-triazole-containing cyclic tetra- and pentapeptides. Eur. J. Org. Chem. 2008, 2008, 2592-2600.
-
(2008)
Eur. J. Org. Chem.
, vol.2008
, pp. 2592-2600
-
-
Springer, J.1
De Cuba, K.R.2
Calvet-Vitale, S.3
Geenevasen, J.A.J.4
Hermkens, P.H.H.5
Hiemstra, H.6
Van Maarseveen, J.H.7
-
19
-
-
0036827575
-
Evaluation of the permeation characteristics of a model opioid peptide, h-tyr-d-ala-gly-phe-d-leu-oh (dadle), and its cyclic prodrugs across the blood-brain barrier using an in situ perfused rat brain model
-
Chen, W.; Yang, J.Z.; Andersen, R.; Nielsen, L.H.; Borchardt, R.T. Evaluation of the permeation characteristics of a model opioid peptide, H-Tyr-D-Ala-Gly-Phe-D-Leu-OH (DADLE), and its cyclic prodrugs across the blood-brain barrier using an in situ perfused rat brain model. J. Pharmacol. Exp. Ther. 2002, 303, 849-857.
-
(2002)
J. Pharmacol. Exp. Ther.
, vol.303
, pp. 849-857
-
-
Chen, W.1
Yang, J.Z.2
Andersen, R.3
Nielsen, L.H.4
Borchardt, R.T.5
-
20
-
-
37848999397
-
Effect of structural and conformational modifications, including backbone cyclization, of hydrophilic hexapeptides on their intestinal permeability and enzymatic stability
-
Hess, S.; Ovadia, O.; Shalev, D.E.; Senderovich, H.; Qadri, B.; Yehezkel, T.; Salitra, Y.; Sheynis, T.; Jelinek, R.; Gilon, C.; et al. Effect of structural and conformational modifications, including backbone cyclization, of hydrophilic hexapeptides on their intestinal permeability and enzymatic stability. J. Med. Chem. 2007, 50, 6201-6211.
-
(2007)
J. Med. Chem.
, vol.50
, pp. 6201-6211
-
-
Hess, S.1
Ovadia, O.2
Shalev, D.E.3
Senderovich, H.4
Qadri, B.5
Yehezkel, T.6
Salitra, Y.7
Sheynis, T.8
Jelinek, R.9
Gilon, C.10
-
21
-
-
33144457849
-
Significant differences in the disposition of cyclic prodrugs of opioid peptides in rats and guinea pigs following iv administration
-
Liederer, B.M.; Phan, K.T.; Ouyang, H.; Borchardt, R.T. Significant differences in the disposition of cyclic prodrugs of opioid peptides in rats and guinea pigs following IV administration. J. Pharm. Sci. 2005, 94, 2676-2687.
-
(2005)
J. Pharm. Sci.
, vol.94
, pp. 2676-2687
-
-
Liederer, B.M.1
Phan, K.T.2
Ouyang, H.3
Borchardt, R.T.4
-
22
-
-
33144469997
-
Effects of amino acid chirality and the chemical linker on the cell permeation characteristics of cyclic prodrugs of opioid peptides
-
Liederer, B.M.; Fuchs, T.; Vander Velde, D.; Siahaan, T.J.; Borchardt, R.T. Effects of amino acid chirality and the chemical linker on the cell permeation characteristics of cyclic prodrugs of opioid peptides. J. Med. Chem. 2006, 49, 1261-1270.
-
(2006)
J. Med. Chem.
, vol.49
, pp. 1261-1270
-
-
Liederer, B.M.1
Fuchs, T.2
Vander Velde, D.3
Siahaan, T.J.4
Borchardt, R.T.5
-
23
-
-
58149194055
-
Structure-activity relationship and metabolic stability studies of backbone cyclization and n-methylation of melanocortin peptides
-
Linde, Y.; Ovadia, O.; Safrai, E.; Xiang, Z.; Portillo, F.P.; Shalev, D.E.; Haskell-Luevano, C.; Hoffman, A.; Gilon, C. Structure-activity relationship and metabolic stability studies of backbone cyclization and N-methylation of melanocortin peptides. Biopolymers 2008, 90, 671-682.
-
(2008)
Biopolymers
, vol.90
, pp. 671-682
-
-
Linde, Y.1
Ovadia, O.2
Safrai, E.3
Xiang, Z.4
Portillo, F.P.5
Shalev, D.E.6
Haskell-Luevano, C.7
Hoffman, A.8
Gilon, C.9
-
24
-
-
50249124786
-
Toward an optimal blood-brain barrier shuttle by synthesis and evaluation of peptide libraries
-
Malakoutikhah, M.; Teixidó, M.; Giralt, E. Toward an optimal blood-brain barrier shuttle by synthesis and evaluation of peptide libraries. J. Med. Chem. 2008, 51, 4881-4889.
-
(2008)
J. Med. Chem.
, vol.51
, pp. 4881-4889
-
-
Malakoutikhah, M.1
Teixidó, M.2
Giralt, E.3
-
25
-
-
67049114267
-
A comparison of the effects of p-glycoprotein inhibitors on the blood-brain barrier permeation of cyclic prodrugs of an opioid peptide (dadle
-
Ouyang, H.; Andersen, T.E.; Chen, W.; Nofsinger, R.; Steffansen, B.; Borchardt, R.T. A comparison of the effects of P-glycoprotein inhibitors on the blood-brain barrier permeation of cyclic prodrugs of an opioid peptide (DADLE). J. Pharm. Sci. 2009, 98, 2227-2236.
-
(2009)
J. Pharm. Sci.
, vol.98
, pp. 2227-2236
-
-
Ouyang, H.1
Andersen, T.E.2
Chen, W.3
Nofsinger, R.4
Steffansen, B.5
Borchardt, R.T.6
-
26
-
-
33644644973
-
Testing the conformational hypothesis of passive membrane permeability using synthetic cyclic peptide diastereomers
-
Rezai, T.; Yu, B.; Millhauser, G.L.; Jacobson, M.P.; Lokey, R.S. Testing the conformational hypothesis of passive membrane permeability using synthetic cyclic peptide diastereomers. J. Am. Chem. Soc. 2006, 128, 2510-2511.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 2510-2511
-
-
Rezai, T.1
Yu, B.2
Millhauser, G.L.3
Jacobson, M.P.4
Lokey, R.S.5
-
27
-
-
27144476545
-
Enhanced metabolic stability and protein-binding properties of artificial a-helices derived from a hydrogen-bond surrogate: Application to bcl-xl
-
Wang, D.; Liao, W.; Arora, P.S. Enhanced metabolic stability and protein-binding properties of artificial a-helices derived from a hydrogen-bond surrogate: Application to Bcl-xL. Angew. Chem. Int. Ed. Engl. 2005, 44, 6525-6529.
-
(2005)
Angew. Chem. Int. Ed. Engl.
, vol.44
, pp. 6525-6529
-
-
Wang, D.1
Liao, W.2
Arora, P.S.3
-
28
-
-
78650746852
-
Methods for the synthesis of macrocycle libraries for drug discovery
-
Terrett, N.K. Methods for the synthesis of macrocycle libraries for drug discovery. Drug Discov. Today Technol. 2010, 7, e97-e104.
-
(2010)
Drug Discov. Today Technol.
, vol.7
-
-
Terrett, N.K.1
-
29
-
-
79955562617
-
Diversity-oriented synthesis of macrocyclic peptidomimetics
-
Isidro-Llobet, A.; Murillo, T.; Bello, P.; Cilibrizzi, A.; Hodgkinson, J.T.; Galloway, W.R.J.D.; Bender, A.; Welch, M.; Spring, D.R. Diversity-oriented synthesis of macrocyclic peptidomimetics. Proc. Natl. Acad. Sci. USA 2011, 108, 6793-6798.
-
(2011)
Proc. Natl. Acad. Sci. USA
, vol.108
, pp. 6793-6798
-
-
Isidro-Llobet, A.1
Murillo, T.2
Bello, P.3
Cilibrizzi, A.4
Hodgkinson, J.T.5
Galloway, W.R.J.D.6
Bender, A.7
Welch, M.8
Spring, D.R.9
-
30
-
-
77949373204
-
Imidazole-4,5-dicarboxylic acid: A versatile scaffold for drug discovery and materials research
-
Baures, P.W. Imidazole-4,5-dicarboxylic acid: A versatile scaffold for drug discovery and materials research. Trends Heterocycl. Chem. 2006, 11, 1-22.
-
(2006)
Trends Heterocycl. Chem.
, vol.11
, pp. 1-22
-
-
Baures, P.W.1
-
31
-
-
77949400178
-
Parallel synthesis of an oligomeric imidazole-4,5-dicarboxamide library
-
Xu, Z.; DiCesare, J.C.; Baures, P.W. Parallel synthesis of an oligomeric imidazole-4,5-dicarboxamide library. J. Comb. Chem. 2010, 12, 248-254.
-
(2010)
J. Comb. Chem.
, vol.12
, pp. 248-254
-
-
Xu, Z.1
DiCesare, J.C.2
Baures, P.W.3
-
32
-
-
59349114704
-
Parallel synthesis of a library of symmetrically and disymmetrically- disubstituted imidazole-4,5-dicarboxamides bearing amino acid esters
-
Solinas, R.; DiCesare, J.C.; Baures, P.W. Parallel synthesis of a library of symmetrically and disymmetrically-disubstituted imidazole-4,5-dicarboxamides bearing amino acid esters. Molecules 2009, 14, 352-363.
-
(2009)
Molecules
, vol.14
, pp. 352-363
-
-
Solinas, R.1
DiCesare, J.C.2
Baures, P.W.3
-
33
-
-
58149269299
-
Parallel synthesis of an imidazole-4,5-dicarboxylic acid library bearing amino acid esters and alkanamines
-
Solinas, R.; DiCesare, J.C.; Baures, P.W. Parallel synthesis of an imidazole-4,5-dicarboxylic acid library bearing amino acid esters and alkanamines. Molecules 2008, 13, 3149-3170.
-
(2008)
Molecules
, vol.13
, pp. 3149-3170
-
-
Solinas, R.1
DiCesare, J.C.2
Baures, P.W.3
-
34
-
-
0031024171
-
Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
-
Lipinski, C.A.; Lombarto, F.; Dominy, B.W.; Feeney, P.J. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv. Drug. Deliv. Rev. 1997, 23, 3-25.
-
(1997)
Adv. Drug. Deliv. Rev.
, vol.23
, pp. 3-25
-
-
Lipinski, C.A.1
Lombarto, F.2
Dominy, B.W.3
Feeney, P.J.4
-
35
-
-
0034461768
-
Drug-like properties and the causes of poor solubility and poor permeability
-
Lipinski, C.A. Drug-like properties and the causes of poor solubility and poor permeability. J. Pharmacol. Toxicol. Methods 2000, 44, 235-249.
-
(2000)
J. Pharmacol. Toxicol. Methods
, vol.44
, pp. 235-249
-
-
Lipinski, C.A.1
-
36
-
-
0035289779
-
Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
-
Lipinski, C.A.; Lombardo, F.; Dominy, B.W.; Feeney, P.J. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv. Drug Deliv. Rev. 2001, 46, 3-26.
-
(2001)
Adv. Drug Deliv. Rev.
, vol.46
, pp. 3-26
-
-
Lipinski, C.A.1
Lombardo, F.2
Dominy, B.W.3
Feeney, P.J.4
-
37
-
-
0037030653
-
Molecular properties that influence the oral bioavailability of drug candidates
-
Veber, D.F.; Johnson, S.R.; Cheng, H.Y.; Smith, B.R.L; Ward, K.W.; Kopple, K.D. Molecular properties that influence the oral bioavailability of drug candidates. J. Med. Chem. 2002, 45, 2615-2623.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 2615-2623
-
-
Veber, D.F.1
Johnson, S.R.2
Cheng, H.Y.3
Smith, B.R.L.4
Ward, K.W.5
Kopple, K.D.6
-
38
-
-
13244266921
-
Lead-and drug-like compounds: The rule of five revolution
-
Lipinski, C.A. Lead- and drug-like compounds: The rule of five revolution. Drug Discov. Today 2004, 1, 337-341.
-
(2004)
Drug Discov. Today
, vol.1
, pp. 337-341
-
-
Lipinski, C.A.1
-
39
-
-
0035966194
-
Elongated multiple electronic cascade and cyclization spacer systems in activatible anticancer prodrugs for enhanced drug release
-
de Groot, F.M.H.; Loos, W.J.; Koekkoek, R.; van Berkom, L.W.A.; Busscher, G.F.; Seelen, A.E.; Albrecht, C.; de Bruijn, P.; Scheeren, H.W. Elongated multiple electronic cascade and cyclization spacer systems in activatible anticancer prodrugs for enhanced drug release. J. Org. Chem. 2001, 66, 8815-8830.
-
(2001)
J. Org. Chem.
, vol.66
, pp. 8815-8830
-
-
De Groot, F.M.H.1
Loos, W.J.2
Koekkoek, R.3
Van Berkom, L.W.A.4
Busscher, G.F.5
Seelen, A.E.6
Albrecht, C.7
De Bruijn, P.8
Scheeren, H.W.9
-
40
-
-
79951846714
-
Evaluation of quinazoline analogues as glucocerebrosidase inhibitors with chaperone activity
-
Marugan, J.J.; Zheng, W.; Motabar, O.; Southall, N.; Goldin, E.; Westbroek, W.; Stubblefield, B.K.; Sidransky, E.; Aungst, R.A.; Lea, W.A.; et al. Evaluation of quinazoline analogues as glucocerebrosidase inhibitors with chaperone activity. J. Med. Chem. 2011, 54, 1033-1058.
-
(2011)
J. Med. Chem.
, vol.54
, pp. 1033-1058
-
-
Marugan, J.J.1
Zheng, W.2
Motabar, O.3
Southall, N.4
Goldin, E.5
Westbroek, W.6
Stubblefield, B.K.7
Sidransky, E.8
Aungst, R.A.9
Lea, W.A.10
-
41
-
-
42149094009
-
Design synthesis, and evaluation of trifluoromethyl ketones as inhibitors of sars-cov 3cl protease
-
Shao, Y.-M.; Yang, W.-B.; Kuo, T.-H.; Tsai, K.-C.; Lin, C.-H.; Yang, A.-S.; Liang, P.-H.; Wong, C.-H. Design, synthesis, and evaluation of trifluoromethyl ketones as inhibitors of SARS-CoV 3CL protease. Bioorg. Med. Chem. 2008, 16, 4652-4660.
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 4652-4660
-
-
Shao, Y.-M.1
Yang, W.-B.2
Kuo, T.-H.3
Tsai, K.-C.4
Lin, C.-H.5
Yang, A.-S.6
Liang, P.-H.7
Wong, C.-H.8
-
42
-
-
36849028500
-
-
Wavefunction, Inc.: Irvine, CA, USA
-
Spartan'06. Wavefunction, Inc.: Irvine, CA, USA, 2006.
-
(2006)
Spartan'06
-
-
-
43
-
-
33746563448
-
Advances in methods and algorithms in a modern quantum chemistry program package
-
Shao, Y.; Molnar, L.F.; Jung, Y.; Kussmann, J.; Ochsenfeld, C.; Brown, S.T.; Gilbert, A.T.B.; Slipchenko, L.V.; Levchenko, S.V.; O'Neill, D.P.; et al. Advances in methods and algorithms in a modern quantum chemistry program package. Phys. Chem. Chem. Phys. 2006, 8, 3172-3191.
-
(2006)
Phys. Chem. Chem. Phys.
, vol.8
, pp. 3172-3191
-
-
Shao, Y.1
Molnar, L.F.2
Jung, Y.3
Kussmann, J.4
Ochsenfeld, C.5
Brown, S.T.6
Gilbert, A.T.B.7
Slipchenko, L.V.8
Levchenko, S.V.9
O'Neill, D.P.10
-
44
-
-
12344250059
-
Intramolecular hydrogen bond strength and pka determination of n,n'-disubstituted imidazole-4,5-dicarboxamides
-
Rush, J.R.; Sandstrom, S.L.; Yang, J.; Davis, R.; Prakash, O.; Baures, P.W. Intramolecular hydrogen bond strength and pKa determination of N,N'-disubstituted imidazole-4,5-dicarboxamides. Org. Lett. 2005, 7, 135-138.
-
(2005)
Org. Lett.
, vol.7
, pp. 135-138
-
-
Rush, J.R.1
Sandstrom, S.L.2
Yang, J.3
Davis, R.4
Prakash, O.5
Baures, P.W.6
-
45
-
-
0141728678
-
Intramolecular hydrogen bonding and intermolecular dimerization in the crystal structures of imidazole-4,5- dicarboxylic acid derivatives
-
Baures, P.W.; Rush, J.R.; Wiznycia, A.V.; Desper, J.; Helfrich, B.A.; Beatty, A.M. Intramolecular hydrogen bonding and intermolecular dimerization in the crystal structures of imidazole-4,5- dicarboxylic acid derivatives. Cryst. Growth Des. 2002, 2, 653-664.
-
(2002)
Cryst. Growth Des.
, vol.2
, pp. 653-664
-
-
Baures, P.W.1
Rush, J.R.2
Wiznycia, A.V.3
Desper, J.4
Helfrich, B.A.5
Beatty, A.M.6
-
46
-
-
0004150157
-
-
University of Göttingen: Göttingen, Germany
-
Sheldrick, G.M. SHELXL-93; University of Göttingen: Göttingen, Germany, 1993.
-
(1993)
SHELXL-93
-
-
Sheldrick, G.M.1
|