Year |
Citation |
Score |
2010 |
Zuev D, Vrudhula VM, Michne JA, Dasgupta B, Pin SS, Huang XS, Wu D, Gao Q, Zhang J, Taber MT, Macor JE, Dubowchik GM. Discovery of 6-chloro-2-trifluoromethyl-7-aryl-7H-imidazo[1,2-a]imidazol-3-ylmethylamines, a novel class of corticotropin-releasing factor receptor type 1 (CRF1R) antagonists. Bioorganic & Medicinal Chemistry Letters. 20: 3669-74. PMID 20471832 DOI: 10.1016/J.Bmcl.2010.04.094 |
0.328 |
|
2009 |
Braun A, Cho IH, Ciblat S, Clyne D, Forgione P, Hart AC, Huang G, Kim J, Modolo I, Paquette LA, Peng X, Pichlmair S, Stewart CA, Wang J, Zuev D. Enantioselective synthesis of structurally intricate and complementary polyoxygenated building blocks of spongistatin 1 (altohyrtin a) Collection of Czechoslovak Chemical Communications. 74: 651-769. DOI: 10.1135/Cccc2008181 |
0.464 |
|
2005 |
Zuev D, Michne JA, Huang H, Beno BR, Wu D, Gao Q, Torrente JR, Xu C, Conway CM, Macor JE, Dubowchik GM. Stereoselective synthesis of new conformationally restricted analogues of a potent CGRP receptor antagonist. Organic Letters. 7: 2465-8. PMID 15932224 DOI: 10.1021/Ol0510062 |
0.403 |
|
2005 |
Zuev D, Michne JA, Pin SS, Zhang J, Taber MT, Dubowchik GM. Optimization of CRF1R binding affinity of 2-(2,4,6-trichlorophenyl)-4-trifluoromethyl-5-aminomethylthiazoles through rapid and selective parallel synthesis. Bioorganic & Medicinal Chemistry Letters. 15: 431-4. PMID 15603967 DOI: 10.1016/J.Bmcl.2004.10.055 |
0.353 |
|
2004 |
Dubowchik GM, Michne JA, Zuev D. An efficient sequence for the preparation of small secondary amine hydrochloride salts for focused library generation without need for distillation or chromatographic purification. Bioorganic & Medicinal Chemistry Letters. 14: 3147-3149. PMID 15149663 DOI: 10.1016/J.Bmcl.2004.04.014 |
0.329 |
|
2003 |
Dubowchik GM, Michne JA, Zuev D, Schwartz W, Scola PM, James CA, Ruediger EH, Pin SS, Burris KD, Balanda LA, Gao Q, Wu D, Fung L, Fiedler T, Browman KE, et al. 2-arylaminothiazoles as high-affinity corticotropin-releasing factor 1 receptor (CRF1R) antagonists: synthesis, binding studies and behavioral efficacy. Bioorganic & Medicinal Chemistry Letters. 13: 3997-4000. PMID 14592493 DOI: 10.1016/J.Bmcl.2003.08.055 |
0.305 |
|
2003 |
Razin VV, Ulin NV, Raev VA, Zadonskaya NY, Zuev DS. Synthesis and Dehydrobromination of 3-Bromomethyl-and 3-Bromo-3- methoxymethylcyclobutane-1-carbonitriles and Methyl 3-Bromomethyl- and 3-Bromo-3-methoxymethylcyclobutane-1-carboxylates Russian Journal of Organic Chemistry. 39: 40-48. DOI: 10.1023/A:1023486427682 |
0.35 |
|
2000 |
Zuev D, Paquette LA. A modular approach to marine macrolide construction. 3. Enantioselective synthesis of the C1-C28 sector of spongistatin 1 (altohyrtin A). Organic Letters. 2: 679-82. PMID 10814408 DOI: 10.1021/Ol0000049 |
0.496 |
|
1997 |
Paquette LA, Zuev D. A modular approach to marine macrolide construction. 1. An enantiocontrolled route to the C1–C12 (AB) spiroacetal sector Tetrahedron Letters. 38: 5115-5118. DOI: 10.1016/S0040-4039(97)01140-4 |
0.509 |
|
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