-
1
-
-
0141789882
-
α-[(9-Fluorenylmethyl) oxy]carbonyl amino acids: synthesis, isolation, characterization, and application to the efficient synthesis of urea peptidomimetics
-
α-[(9-Fluorenylmethyl) oxy]carbonyl amino acids: synthesis, isolation, characterization, and application to the efficient synthesis of urea peptidomimetics. J. Org. Chem. 2003; 68: 7274-7280.
-
(2003)
J. Org. Chem.
, vol.68
, pp. 7274-7280
-
-
Patil, B.S.1
Vasanthakumar, G.R.2
Sureshbabu, V.V.3
-
3
-
-
36849093924
-
An efficient conversion of the carboxylic group of N-Fmoc α-amino acids/peptide acids into N-formamides employing isocyanates as key intermediates
-
Sudarshan NS, Narendra N, Hemantha HP, Sureshbabu VV. An efficient conversion of the carboxylic group of N-Fmoc α-amino acids/peptide acids into N-formamides employing isocyanates as key intermediates. J. Org. Chem 2007; 72: 9804-9807.
-
(2007)
J. Org. Chem
, vol.72
, pp. 9804-9807
-
-
Sudarshan, N.S.1
Narendra, N.2
Hemantha, H.P.3
Sureshbabu, V.V.4
-
4
-
-
58149302872
-
Chiral N-Fmoc-β-amino alkyl isonitriles derived from amino acids: first synthesis and application in 1-substituted tetrazole synthesis
-
Sureshbabu VV, Narendra N, Nagendra G. Chiral N-Fmoc-β-amino alkyl isonitriles derived from amino acids: first synthesis and application in 1-substituted tetrazole synthesis. J. Org. Chem. 2009; 74: 153-157.
-
(2009)
J. Org. Chem.
, vol.74
, pp. 153-157
-
-
Sureshbabu, V.V.1
Narendra, N.2
Nagendra, G.3
-
5
-
-
68049103235
-
N-Urethane-protected amino alkyl isothiocyanates: synthesis, isolation, characterization, and application to the synthesis of thioureidopeptides
-
Sureshbabu VV, Naik SA, Hemantha HP, Narendra N, Das U, Row TNG. N-Urethane-protected amino alkyl isothiocyanates: synthesis, isolation, characterization, and application to the synthesis of thioureidopeptides. J. Org. Chem. 2009; 74: 5260-5266.
-
(2009)
J. Org. Chem.
, vol.74
, pp. 5260-5266
-
-
Sureshbabu, V.V.1
Naik, S.A.2
Hemantha, H.P.3
Narendra, N.4
Das, U.5
Row, T.N.G.6
-
6
-
-
13944277208
-
Pseudo-peptides in Drug Discovery
-
Nielsen, PE (ed.). WILEY-VCH: Weinheim.
-
Guichard G. Pseudo-peptides in Drug Discovery. Nielsen, PE (ed.). WILEY-VCH: Weinheim, 2004; 33-120.
-
(2004)
, pp. 33-120
-
-
Guichard, G.1
-
7
-
-
78650461320
-
Synthesis of Peptides and Peptidomimetics (Houben-Weyl)
-
Goodman, M., Felix, A. Moroder L. and Toniolo C. (eds.). Georg Thieme Verlag: Stuttgart, Germany, and references cited therein.
-
Synthesis of Peptides and Peptidomimetics (Houben-Weyl). Goodman, M., Felix, A. Moroder L. and Toniolo C. (eds.). Georg Thieme Verlag: Stuttgart, Germany, 2003; Vol. E22c and references cited therein.
-
(2003)
, vol.E22c
-
-
-
8
-
-
0028057975
-
An unnatural biopolymer
-
Lam PY, Jadhav PK, Eyermann CJ, Hodge CN, Ru Y, Bacheler LT, Meek JL, Otto MJ, Rayner MM, Wong YN, Chang CH, Weber PC, Jackson DA, Sharpe TR, Erickson-Viitanen S. An unnatural biopolymer. Science 1994; 263: 380-384.
-
(1994)
Science
, vol.263
, pp. 380-384
-
-
Lam, P.Y.1
Jadhav, P.K.2
Eyermann, C.J.3
Hodge, C.N.4
Ru, Y.5
Bacheler, L.T.6
Meek, J.L.7
Otto, M.J.8
Rayner, M.M.9
Wong, Y.N.10
Chang, C.H.11
Weber, P.C.12
Jackson, D.A.13
Sharpe, T.R.14
Erickson-Viitanen, S.15
-
9
-
-
33751391068
-
An improved method for the synthesis of enantiomerically pure amino acid ester isocyanates
-
Nowick JS, Powell NA, Nguyen TM, Noronha G. An improved method for the synthesis of enantiomerically pure amino acid ester isocyanates. J. Org. Chem. 1992; 57: 7364-7366.
-
(1992)
J. Org. Chem.
, vol.57
, pp. 7364-7366
-
-
Nowick, J.S.1
Powell, N.A.2
Nguyen, T.M.3
Noronha, G.4
-
10
-
-
0033534574
-
A peptide/oligourea/azapeptide hybrid that adopts a hairpin turn
-
Soth MJ, Nowick JS. A peptide/oligourea/azapeptide hybrid that adopts a hairpin turn. J. Org. Chem. 1999; 64: 276-281.
-
(1999)
J. Org. Chem.
, vol.64
, pp. 276-281
-
-
Soth, M.J.1
Nowick, J.S.2
-
11
-
-
0029670181
-
An artificial β-sheet comprising a molecular scaffold, a β-strand mimic and a peptide strand
-
Nowick JS, Holmes DL, Mackin G, Noronha G, Shaka AJ, Smith EM. An artificial β-sheet comprising a molecular scaffold, a β-strand mimic and a peptide strand. J. Am. Chem. Soc. 1996; 118: 2764-2765.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 2764-2765
-
-
Nowick, J.S.1
Holmes, D.L.2
Mackin, G.3
Noronha, G.4
Shaka, A.J.5
Smith, E.M.6
-
12
-
-
0001005576
-
Synthesis of peptide isocyanates and isothiocyanates
-
Nowick JS, Holmes DL, Noronha G, Smith EM, Nguyen TM, Huang SL. Synthesis of peptide isocyanates and isothiocyanates. J. Org. Chem. 1996; 61: 3929-3934.
-
(1996)
J. Org. Chem.
, vol.61
, pp. 3929-3934
-
-
Nowick, J.S.1
Holmes, D.L.2
Noronha, G.3
Smith, E.M.4
Nguyen, T.M.5
Huang, S.L.6
-
13
-
-
41649117681
-
A new efficient synthesis of isothiocyanates from amines using di-tert-butyl dicarbonate
-
Munch H, Hansen JS, Pittelkow M, Christensen JB, Boas U. A new efficient synthesis of isothiocyanates from amines using di-tert-butyl dicarbonate. Tetrahedron Lett. 2008; 49: 3117-3119.
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 3117-3119
-
-
Munch, H.1
Hansen, J.S.2
Pittelkow, M.3
Christensen, J.B.4
Boas, U.5
-
14
-
-
84984583119
-
Organoselenium and organotellurium compounds: Toxicology and pharmacology
-
Nogueira CW, Zeni G, Rocha JBT. Organoselenium and organotellurium compounds: Toxicology and pharmacology. Chem. Rev. 2004; 104: 6255-6285.
-
(2004)
Chem. Rev.
, vol.104
, pp. 6255-6285
-
-
Nogueira, C.W.1
Zeni, G.2
Rocha, J.B.T.3
-
15
-
-
0035385139
-
Chemistry of biologically important synthetic organoselenium compounds
-
Mugesh G, du Mont WW, Sies H. Chemistry of biologically important synthetic organoselenium compounds. Chem. Rev. 2001; 101: 2125-2179.
-
(2001)
Chem. Rev.
, vol.101
, pp. 2125-2179
-
-
Mugesh, G.1
du Mont, W.W.2
Sies, H.3
-
16
-
-
22544483572
-
Selenium-containing heterocycles from isoselenocyanates: synthesis of 1,3-selenazolidine and perhydro-1,3-selenazine derivatives
-
Sommen GL, Linden A, Heimgartner H. Selenium-containing heterocycles from isoselenocyanates: synthesis of 1, 3-selenazolidine and perhydro-1, 3-selenazine derivatives. Eur. J. Org. Chem. 2005; 3128-3137.
-
(2005)
Eur. J. Org. Chem.
, pp. 3128-3137
-
-
Sommen, G.L.1
Linden, A.2
Heimgartner, H.3
-
17
-
-
60149096190
-
Synthesis of sugar-derived isoselenocyanates, selenoureas and selenazoles
-
Lopez O, Maza S, Ulgar V, Maya I, Fernandez-Bolanos JG. Synthesis of sugar-derived isoselenocyanates, selenoureas and selenazoles. Tetrahedron 2009; 65: 2556-2566.
-
(2009)
Tetrahedron
, vol.65
, pp. 2556-2566
-
-
Lopez, O.1
Maza, S.2
Ulgar, V.3
Maya, I.4
Fernandez-Bolanos, J.G.5
-
19
-
-
0002770696
-
Selenium: Its Molecular Biology and Role in Human Health
-
Hatfield (ed.). Kluwer: New York.
-
Combs GF, Lu J. Selenium: Its Molecular Biology and Role in Human Health. Hatfield (ed.). Kluwer: New York, 2001; 205-218.
-
(2001)
, pp. 205-218
-
-
Combs, G.F.1
Lu, J.2
-
20
-
-
45549086618
-
Synthesis of selenocysteine and its derivatives with an emphasis on selenenylsulfide (-Se-S-) formation
-
Wessjohann LA, Schneider A. Synthesis of selenocysteine and its derivatives with an emphasis on selenenylsulfide (-Se-S-) formation. Chem. Biodiver. 2008; 5: 375-388.
-
(2008)
Chem. Biodiver.
, vol.5
, pp. 375-388
-
-
Wessjohann, L.A.1
Schneider, A.2
-
21
-
-
0034808792
-
Selenocystein in native chemical ligation and expressed protein ligation
-
Hondal RJ, Nilsson BL, Raines RT. Selenocystein in native chemical ligation and expressed protein ligation. J. Am. Chem. Soc. 2001; 123: 5140-5141.
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 5140-5141
-
-
Hondal, R.J.1
Nilsson, B.L.2
Raines, R.T.3
-
22
-
-
33947094332
-
Gas chromatographic determination and purification of carbon diselenide
-
Marquart JR, Belford RL. Gas chromatographic determination and purification of carbon diselenide. Anal. Chem. 1978; 50: 656-657.
-
(1978)
Anal. Chem.
, vol.50
, pp. 656-657
-
-
Marquart, J.R.1
Belford, R.L.2
-
23
-
-
0003231455
-
Transition-metal thiocarbonyls and selenocarbonyls
-
Butler IS. Transition-metal thiocarbonyls and selenocarbonyls. Acc. Chem. Res. 1977; 10: 359-365.
-
(1977)
Acc. Chem. Res.
, vol.10
, pp. 359-365
-
-
Butler, I.S.1
-
25
-
-
0000279927
-
Synthesis of aliphatic isoselenocyanates by the reaction of aliphatic isocyanides with selenium in the presence of triethylamine
-
Sonoda N, Yamamoto G, Tsutsumi S. Synthesis of aliphatic isoselenocyanates by the reaction of aliphatic isocyanides with selenium in the presence of triethylamine. Bull. Chem. Soc. Jpn. 1972; 45: 2937-2938.
-
(1972)
Bull. Chem. Soc. Jpn.
, vol.45
, pp. 2937-2938
-
-
Sonoda, N.1
Yamamoto, G.2
Tsutsumi, S.3
-
26
-
-
0009295806
-
Alkyl isoselenocyanates and related compounds
-
Franklin WJ, Werer RL. Alkyl isoselenocyanates and related compounds. Tetrahedron Lett. 1965; 6: 3003-3008.
-
(1965)
Tetrahedron Lett.
, vol.6
, pp. 3003-3008
-
-
Franklin, W.J.1
Werer, R.L.2
-
27
-
-
33748812051
-
Synthesis and reactions of vinyl isoselenocyanates
-
Banert K, Toth C. Synthesis and reactions of vinyl isoselenocyanates. Angew Chem. Int. Ed. Engl. 1995; 34: 1627-1629.
-
(1995)
Angew Chem. Int. Ed. Engl.
, vol.34
, pp. 1627-1629
-
-
Banert, K.1
Toth, C.2
-
28
-
-
0009230476
-
Trimethylsilyl isoselenocyanat
-
Burger H, Goetze U. Trimethylsilyl isoselenocyanat. J. Organomet. Chem. 1967; 10: 380-382.
-
(1967)
J. Organomet. Chem.
, vol.10
, pp. 380-382
-
-
Burger, H.1
Goetze, U.2
-
29
-
-
0033588297
-
Preparation of isoselenocyanate and synthesis of carbodiimide by oxidation of selenourea
-
Koketsu M, Suzuki N, Ishihara H. Preparation of isoselenocyanate and synthesis of carbodiimide by oxidation of selenourea. J. Org. Chem. 1999; 64: 6473-6475.
-
(1999)
J. Org. Chem.
, vol.64
, pp. 6473-6475
-
-
Koketsu, M.1
Suzuki, N.2
Ishihara, H.3
-
30
-
-
0028089034
-
A convenient and high yielding procedure for the preparation of isoselenocyanates. Synthesis and reactivity of O-alkylselenocarbamates
-
Barton DHR, Parekh SI, Tajbakhsh M, Theodorakis EA, Tse CL. A convenient and high yielding procedure for the preparation of isoselenocyanates. Synthesis and reactivity of O-alkylselenocarbamates. Tetrahedron 1994; 50: 639-654.
-
(1994)
Tetrahedron
, vol.50
, pp. 639-654
-
-
Barton, D.H.R.1
Parekh, S.I.2
Tajbakhsh, M.3
Theodorakis, E.A.4
Tse, C.L.5
-
31
-
-
57549111251
-
On the preparation of enantiomerically pure isonitriles from amino acid esters and peptides
-
Zhu J, Wu X, Danishefsky SJ. On the preparation of enantiomerically pure isonitriles from amino acid esters and peptides. Tetrahedron Lett. 2009; 50: 577-579.
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 577-579
-
-
Zhu, J.1
Wu, X.2
Danishefsky, S.J.3
-
32
-
-
60849117540
-
Nonracemizable isocyanoacetates for multicomponent reactions
-
Zhdanko AG, Nenajdenko VG. Nonracemizable isocyanoacetates for multicomponent reactions. J. Org. Chem. 2009; 74: 884-887.
-
(2009)
J. Org. Chem.
, vol.74
, pp. 884-887
-
-
Zhdanko, A.G.1
Nenajdenko, V.G.2
-
33
-
-
84890597202
-
Multicomponent Reactions
-
Zhu J. and Bienayme H. (eds.). WILEY-VCH, Verlag GmbH: Germany.
-
Multicomponent Reactions. Zhu J. and Bienayme H. (eds.). WILEY-VCH, Verlag GmbH: Germany, 2005.
-
(2005)
-
-
-
34
-
-
2542509173
-
Multicomponent reactions with isocyanides
-
Domling A, Ugi I. Multicomponent reactions with isocyanides. Angew. Chem. Int. Ed. 2000; 39: 3168-3210..
-
(2000)
Angew. Chem. Int. Ed.
, vol.39
, pp. 3168-3210
-
-
Domling, A.1
Ugi, I.2
-
35
-
-
78650491596
-
+-imidazolium) bis(methanesulphonate), a versatile dehydrating reagent
-
+-imidazolium) bis(methanesulphonate), a versatile dehydrating reagent. J. Chem. Res. 1982; 79.
-
(1982)
J. Chem. Res.
, pp. 79
-
-
Giesemann, G.1
Ugi, I.2
-
36
-
-
0033546342
-
A new class of convertible isocyanides in the Ugi four-component reaction
-
Lindhorst T, Bock H, Ugi I. A new class of convertible isocyanides in the Ugi four-component reaction. Tetrahedron 1999; 55: 7411-7420.
-
(1999)
Tetrahedron
, vol.55
, pp. 7411-7420
-
-
Lindhorst, T.1
Bock, H.2
Ugi, I.3
-
38
-
-
0020211577
-
From isocyanides via four-component condensations to antibiotic syntheses
-
Ugi I. From isocyanides via four-component condensations to antibiotic syntheses. Angew. Chem. Int. Ed 1982; 21: 810-819.
-
(1982)
Angew. Chem. Int. Ed
, vol.21
, pp. 810-819
-
-
Ugi, I.1
-
39
-
-
33750084573
-
-
Lehnhoff S, Goebel M, Karl RM, Klosel R, Ugi I. Angew. Chem. Int. Ed. 1995; 34: 1104-1107.
-
(1995)
Angew. Chem. Int. Ed.
, vol.34
, pp. 1104-1107
-
-
Lehnhoff, S.1
Goebel, M.2
Karl, R.M.3
Klosel, R.4
Ugi, I.5
-
40
-
-
85005647840
-
Isocyanide synthesis with phosphoryl chloride and diisopropylamine
-
Obrecht R, Ugi I. Isocyanide synthesis with phosphoryl chloride and diisopropylamine. Synthesis 1985; 4: 400-402.
-
(1985)
Synthesis
, vol.4
, pp. 400-402
-
-
Obrecht, R.1
Ugi, I.2
-
41
-
-
20344370972
-
The partial retro-inverso modification: a road traveled together
-
Chorev M. The partial retro-inverso modification: a road traveled together. Peptide Sci. (Biopolymers) 2005; 80: 67-84.
-
(2005)
Peptide Sci. (Biopolymers)
, vol.80
, pp. 67-84
-
-
Chorev, M.1
-
42
-
-
33748247569
-
Conformational requirements for sweet-tasting peptides and peptidomimetics
-
Yamazaki T, Benedetti E, Kent D, Goodman M. Conformational requirements for sweet-tasting peptides and peptidomimetics. Angew. Chem. Int. Ed. 1994; 33: 1437-1451.
-
(1994)
Angew. Chem. Int. Ed.
, vol.33
, pp. 1437-1451
-
-
Yamazaki, T.1
Benedetti, E.2
Kent, D.3
Goodman, M.4
-
43
-
-
52649161209
-
Microwave assisted facile synthesis of amino acid benzyl ester p-toluenesulfonate and hydrochloride salts
-
Vasanthakumar GR, Patil BS, Sureshbabu VV. Microwave assisted facile synthesis of amino acid benzyl ester p-toluenesulfonate and hydrochloride salts. Lett. Pept. Sci. 2002; 9: 207-209.
-
(2002)
Lett. Pept. Sci.
, vol.9
, pp. 207-209
-
-
Vasanthakumar, G.R.1
Patil, B.S.2
Sureshbabu, V.V.3
-
46
-
-
34247144592
-
Hybrid peptide design. Hydrogen bonded conformations in peptides containing the stereochemically constrained γ-amino acid residue, gabapentin
-
Aravinda S, Ananda K, Chatterjee S, Shamala N, Balaram P. Hybrid peptide design. Hydrogen bonded conformations in peptides containing the stereochemically constrained γ-amino acid residue, gabapentin. J. Am. Chem. Soc. 2007; 129: 4039-4048.
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 4039-4048
-
-
Aravinda, S.1
Ananda, K.2
Chatterjee, S.3
Shamala, N.4
Balaram, P.5
-
47
-
-
0742304175
-
Synthesis of polysubstituted 4,5,6,7-tetrahydrofuro[2,3-c]pyridines by a novel multicomponent reaction
-
Fayol A, Zhu J. Synthesis of polysubstituted 4, 5, 6, 7-tetrahydrofuro[2, 3-c]pyridines by a novel multicomponent reaction. Org. Lett. 2004; 6: 115-118.
-
(2004)
Org. Lett.
, vol.6
, pp. 115-118
-
-
Fayol, A.1
Zhu, J.2
-
48
-
-
33845266730
-
Parallel synthesis of arrays of amino acid-derived isocyanoamides useful as starting materials in IMCR
-
Domling A, Beck B, Fuchs T, Yazbak A. Parallel synthesis of arrays of amino acid-derived isocyanoamides useful as starting materials in IMCR. J. Comb. Chem. 2006; 8: 872-880.
-
(2006)
J. Comb. Chem.
, vol.8
, pp. 872-880
-
-
Domling, A.1
Beck, B.2
Fuchs, T.3
Yazbak, A.4
-
49
-
-
12344293588
-
Synthesis of α-isocyano-alkyl(aryl) acetamides and their use in the multicomponent synthesis of 5-aminooxazole, pyrrolo[3,4-b]pyridin-5-one and 4,5,6,7-tetrahydrofuro[2,3-c]pyridine
-
Fayol A, Housseman C, Sun X, Janvier P, Bienayme H, Zhu J. Synthesis of α-isocyano-alkyl(aryl) acetamides and their use in the multicomponent synthesis of 5-aminooxazole, pyrrolo[3, 4-b]pyridin-5-one and 4, 5, 6, 7-tetrahydrofuro[2, 3-c]pyridine. Synthesis 2005; 161-165.
-
(2005)
Synthesis
, pp. 161-165
-
-
Fayol, A.1
Housseman, C.2
Sun, X.3
Janvier, P.4
Bienayme, H.5
Zhu, J.6
-
50
-
-
0037039947
-
Reaction of N,N-dimethylselenocarbamoyl chloride with neucleophiles. Preparation of diselenocarbamates, selenothiocarbamates, and selenoureas
-
Koketsu M, Fukuta Y, Ishihara H. Reaction of N, N-dimethylselenocarbamoyl chloride with neucleophiles. Preparation of diselenocarbamates, selenothiocarbamates, and selenoureas. J. Org. Chem. 2002; 67: 1008-1011.
-
(2002)
J. Org. Chem.
, vol.67
, pp. 1008-1011
-
-
Koketsu, M.1
Fukuta, Y.2
Ishihara, H.3
-
51
-
-
0035083123
-
Deprotonation of hydrochloride salts of amino acid esters and peptide esters using commercial zinc dust
-
Ananda K, Sureshbabu VV. Deprotonation of hydrochloride salts of amino acid esters and peptide esters using commercial zinc dust. J. Pept. Res. 2001; 57: 223-226.
-
(2001)
J. Pept. Res.
, vol.57
, pp. 223-226
-
-
Ananda, K.1
Sureshbabu, V.V.2
-
52
-
-
34547204175
-
Enantioselective Organocatalysis
-
Dalko PI. (ed.). WILEY-VCH, Verlag: Germany.
-
Enantioselective Organocatalysis. Dalko PI. (ed.). WILEY-VCH, Verlag: Germany, 2007.
-
(2007)
-
-
-
53
-
-
38349135345
-
Small-molecule H-bond donors in asymmetric catalysis
-
Doyle AG, Jacobsen EN. Small-molecule H-bond donors in asymmetric catalysis. Chem. Rev 2007; 107: 5713-5743.
-
(2007)
Chem. Rev
, vol.107
, pp. 5713-5743
-
-
Doyle, A.G.1
Jacobsen, E.N.2
-
54
-
-
27444433708
-
Small peptides as modular catalysts for the direct asymmetric aldol reaction: ancient peptides with aldolase enzyme activity
-
Zou W, Ibrahem I, Dziedzic P, Sunden H, Cordova A. Small peptides as modular catalysts for the direct asymmetric aldol reaction: ancient peptides with aldolase enzyme activity. Chem. Commun. 2005; 4946-4948.
-
(2005)
Chem. Commun.
, pp. 4946-4948
-
-
Zou, W.1
Ibrahem, I.2
Dziedzic, P.3
Sunden, H.4
Cordova, A.5
-
55
-
-
46949091946
-
Novel bifunctional chiral thiourea catalyzed highly enantioselective aza-Henry reaction
-
Wang C, Zhou Z, Tang C. Novel bifunctional chiral thiourea catalyzed highly enantioselective aza-Henry reaction. Org. Lett. 2008; 10: 1707-1710.
-
(2008)
Org. Lett.
, vol.10
, pp. 1707-1710
-
-
Wang, C.1
Zhou, Z.2
Tang, C.3
-
56
-
-
33750738055
-
Thiourea and selenourea and their applications
-
Koketsu M, Ishihara H. Thiourea and selenourea and their applications. Curr. Org. Synth 2006; 3: 439-455.
-
(2006)
Curr. Org. Synth
, vol.3
, pp. 439-455
-
-
Koketsu, M.1
Ishihara, H.2
-
57
-
-
0028028227
-
Bicyclic hydantoins with a bridgehead nitrogen. Comparison of anticonvulsant activities with binding to the neuronal voltage-dependent sodium channel
-
Brouillete WJ, Jestkov VP, Brown ML, Akthar MS, Delorey TM, Brown GB. Bicyclic hydantoins with a bridgehead nitrogen. Comparison of anticonvulsant activities with binding to the neuronal voltage-dependent sodium channel. J. Med. Chem. 1994; 37: 3289-3293.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 3289-3293
-
-
Brouillete, W.J.1
Jestkov, V.P.2
Brown, M.L.3
Akthar, M.S.4
Delorey, T.M.5
Brown, G.B.6
-
58
-
-
67650650998
-
Synthesis of hydantoins and thiohydantoins spiro-fused to pyrrolidines: drug like molecules based on the 2-aylethyl amine scaffold
-
Blanco-Ania D, Hermkens PHH, Sliedregt LAJM, Scheeren HW, Rutjes FPLT. Synthesis of hydantoins and thiohydantoins spiro-fused to pyrrolidines: drug like molecules based on the 2-aylethyl amine scaffold. J. Comb. Chem. 2009; 11: 527-538.
-
(2009)
J. Comb. Chem.
, vol.11
, pp. 527-538
-
-
Blanco-Ania, D.1
Hermkens, P.H.H.2
Sliedregt, L.A.J.M.3
Scheeren, H.W.4
Rutjes, F.P.L.T.5
-
59
-
-
34147167373
-
A facile preparation of selenohydantoins using isoselenocyanato
-
Koketsu M, Takahashi A, Ishihara H. A facile preparation of selenohydantoins using isoselenocyanato. J. Heterocycl. Chem. 2007; 44: 79-81.
-
(2007)
J. Heterocycl. Chem.
, vol.44
, pp. 79-81
-
-
Koketsu, M.1
Takahashi, A.2
Ishihara, H.3
|