Year |
Citation |
Score |
2010 |
VERDAGUER X, BERK SC, BUCHWALD SL. ChemInform Abstract: Catalytic Method for the Reduction of Lactones to Lactols. Cheminform. 27: no-no. DOI: 10.1002/chin.199616072 |
0.51 |
|
2010 |
BARR KJ, BERK SC, BUCHWALD SL. ChemInform Abstract: Titanocene-Catalyzed Reduction of Esters Using Polymethylhydrosiloxane as the Stoichiometric Reductant. Cheminform. 26: no-no. DOI: 10.1002/chin.199505085 |
0.722 |
|
2010 |
BERK SC, GROSSMAN RB, BUCHWALD SL. ChemInform Abstract: Titanocene-Catalyzed Conversion of Enynes to Bicyclic Cyclopentenones. Cheminform. 24: no-no. DOI: 10.1002/chin.199340158 |
0.673 |
|
2010 |
BERK SC, KREUTZER KA, BUCHWALD SL. ChemInform Abstract: A Catalytic Method for the Reduction of Esters to Alcohols. Cheminform. 22: no-no. DOI: 10.1002/chin.199141081 |
0.56 |
|
2003 |
Lynch CL, Willoughby CA, Hale JJ, Holson EJ, Budhu RJ, Gentry AL, Rosauer KG, Caldwell CG, Chen P, Mills SG, MacCoss M, Berk S, Chen L, Chapman KT, Malkowitz L, et al. 1,3,4-Trisubstituted pyrrolidine CCR5 receptor antagonists: modifications of the arylpropylpiperidine side chains. Bioorganic & Medicinal Chemistry Letters. 13: 119-23. PMID 12467630 DOI: 10.1016/S0960-894X(02)00829-6 |
0.663 |
|
2001 |
Willoughby CA, Berk SC, Rosauer KG, Degrado S, Chapman KT, Gould SL, Springer MS, Malkowitz L, Schleif WA, Hazuda D, Miller M, Kessler J, Danzeisen R, Holmes K, Lineberger J, et al. Combinatorial synthesis of CCR5 antagonists. Bioorganic & Medicinal Chemistry Letters. 11: 3137-41. PMID 11720860 DOI: 10.1016/S0960-894X(01)00652-7 |
0.608 |
|
2001 |
Yates N, Wislocki D, Roberts A, Berk S, Klatt T, Shen DM, Willoughby C, Rosauer K, Chapman K, Griffin P. Mass spectrometry screening of combinatorial mixtures, correlation of measured and predicted electrospray ionization spectra. Analytical Chemistry. 73: 2941-51. PMID 11467539 DOI: 10.1021/Ac010021R |
0.613 |
|
1997 |
Verdaguer X, Hansen MC, Berk SC, Buchwald SL. Titanocene-Catalyzed Reduction of Lactones to Lactols. The Journal of Organic Chemistry. 62: 8522-8528. PMID 11671995 DOI: 10.1021/Jo971560S |
0.708 |
|
1996 |
Hicks FA, Berk SC, Buchwald SL. A Practical Titanium-Catalyzed Synthesis of Bicyclic Cyclopentenones and Allylic Amines. The Journal of Organic Chemistry. 61: 2713-2718. PMID 11667103 DOI: 10.1021/Jo951763L |
0.736 |
|
1995 |
Verdaguer X, Berk SC, Buchwald SL. Catalytic method for the reduction of lactones to lactols Journal of the American Chemical Society. 117: 12641-12642. DOI: 10.1021/Ja00155A031 |
0.552 |
|
1995 |
BERK SC, GROSSMAN RB, BUCHWALD SL. ChemInform Abstract: Development of a Titanocene-Catalyzed Enyne Cyclization/Isocyanide Insertion Reaction. Cheminform. 26: no-no. DOI: 10.1002/chin.199516102 |
0.648 |
|
1994 |
Barr KJ, Berk SC, Buchwald SL. Titanocene-Catalyzed Reduction of Esters Using Polymethylhydrosiloxane as the Stoichiometric Reductant The Journal of Organic Chemistry. 59: 4323-4326. DOI: 10.1021/Jo00094A056 |
0.734 |
|
1994 |
Berk SC, Grossman RB, Buchwald SL. Development of a Titanocene-Catalyzed Enyne Cyclization/Isocyanide Insertion Reaction Journal of the American Chemical Society. 116: 8593-8601. DOI: 10.1021/Ja00098A020 |
0.662 |
|
1994 |
Barr KJ, Berk SC, Buchwald SL. Titanocene-catalyzed reduction of esters using polymethylhydrosiloxane as the stoichiometric reductant Journal of Organic Chemistry. 59: 4323-4326. |
0.698 |
|
1994 |
Berk SC, Grossman RB, Buchwald SL. Development of a titanocene-catalyzed enyne cyclization/isocyanide insertion reaction Journal of the American Chemical Society. 116: 8593-8601. |
0.584 |
|
1993 |
Berk SC, Buchwald SL. An air-stable catalyst system for the conversion of esters to alcohols. [Erratum to document cited in CA117(3):25599z] The Journal of Organic Chemistry. 58: 3221-3221. DOI: 10.1021/Jo00063A060 |
0.539 |
|
1993 |
Berk SC, Grossman RB, Buchwald SL. Titanocene-catalyzed conversion of enynes to bicyclic cyclopentenones Journal of the American Chemical Society. 115: 4912-4913. DOI: 10.1021/Ja00064A071 |
0.697 |
|
1993 |
Berk SC, Grossman RB, Buchwald SL. Titanocene-catalyzed conversion of enynes to bicyclic cyclopentenones Journal of the American Chemical Society. 115: 4912-4913. |
0.632 |
|
1992 |
Berk SC, Buchwald SL. An air-stable catalyst system for the conversion of esters to alcohols The Journal of Organic Chemistry. 57: 3751-3753. DOI: 10.1021/Jo00040A001 |
0.589 |
|
1992 |
BERK SC, BUCHWALD SL. ChemInform Abstract: An Air-Stable Catalyst System for the Conversion of Esters to Alcohols. Cheminform. 23: no-no. DOI: 10.1002/chin.199251118 |
0.53 |
|
1992 |
Berk SC, Buchwald SL. An air-stable catalyst system for the conversion of esters to alcohols Journal of Organic Chemistry. 57: 3751-3753. |
0.362 |
|
1991 |
Berk SC, Kreutzer KA, Buchwald SL. A catalytic method for the reduction of esters to alcohols Journal of the American Chemical Society. 113: 5093-5095. DOI: 10.1021/Ja00013A074 |
0.739 |
|
1991 |
Berk SC, Kreutzer KA, Buchwald SL. A Catalytic Method for the Reduction of Esters to Alcohols Journal of the American Chemical Society. 113: 5093-5095. |
0.749 |
|
1990 |
Berk SC, Yeh MCP, Jeong N, Knochel P. Preparation and Reactions of Functionalized Benzylic Organometallics of Zinc And Copper Organometallics. 9: 3053-3064. DOI: 10.1021/Om00162A016 |
0.514 |
|
1988 |
Berk SC, Knochel P, Yeh MCP. General Approach to Highly Functionalized Benzylic Organometallics of Zinc and Copper Journal of Organic Chemistry. 53: 5789-5791. DOI: 10.1021/Jo00259A038 |
0.348 |
|
1988 |
Knochel P, Yeh MCP, Berk SC, Talbert J. Synthesis and reactivity toward acyl chlorides and enones of the new highly functionalized copper reagents RCu(CN)ZnI Journal of Organic Chemistry. 53: 2390-2392. DOI: 10.1021/Jo00245A057 |
0.345 |
|
1988 |
Yeh MCP, Knochel P, Butler WM, Berk SC. 1,4-Additions of the highly functionalized copper reagents RCu(CN)ZnI · 2 BFP3 to trisubstituted enones. A new BF3 promoted cyclization reaction Tetrahedron Letters. 29: 6693-6696. DOI: 10.1016/S0040-4039(00)82430-2 |
0.478 |
|
Low-probability matches (unlikely to be authored by this person) |
2004 |
Ma Y, Margarida L, Brookes J, Makara GM, Berk SC. Combinatorial synthesis of substituted biaryls and heterocyclic arylamines. Journal of Combinatorial Chemistry. 6: 426-30. PMID 15132604 DOI: 10.1021/cc0340731 |
0.295 |
|
2002 |
Flynn DL, Hanson PR, Berk SC, Makara GM. New developments in chemical library synthesis. Norbornenyl tags for use in phase-switching, sequestration, capture-release and soluble support applications. Current Opinion in Drug Discovery & Development. 5: 571-9. PMID 12197315 |
0.28 |
|
1990 |
Berk SC, Yeh MCP, Jeong N, Knochel P. Preparation and reactions of functionalized benzylic organometallics of zinc and copper Organometallics. 9: 3053-3064. |
0.25 |
|
1988 |
Knochel P, Yeh MCP, Berk SC, Talbert J. Synthesis and reactivity toward acyl chlorides and enones of the new highly functionalized copper reagents RCu(CN)ZnI Journal of Organic Chemistry. 53: 2390-2392. |
0.227 |
|
2005 |
Schell P, Richards MP, Hanson K, Berk SC, Makara GM. Versatile solid-phase synthesis of trisubstituted 1H-pyrido[2,3-d]pyrimidin-4-ones and related heterocycles. Journal of Combinatorial Chemistry. 7: 96-8. PMID 15638487 DOI: 10.1021/cc049921m |
0.164 |
|
2002 |
Flynn DL, Berk SC, Makara GM. Recent advances in chemical library synthesis methodology. Current Opinion in Drug Discovery & Development. 5: 580-93. PMID 12197316 |
0.151 |
|
1988 |
Berk SC, Knochel P, Yeh MCP. General approach to highly functionalized benzylic organometallics of zinc and copper Journal of Organic Chemistry. 53: 5789-5791. |
0.11 |
|
2009 |
Kattar SD, Surdi LM, Zabierek A, Methot JL, Middleton RE, Hughes B, Szewczak AA, Dahlberg WK, Kral AM, Ozerova N, Fleming JC, Wang H, Secrist P, Harsch A, Hamill JE, ... ... Berk SC, et al. Parallel medicinal chemistry approaches to selective HDAC1/HDAC2 inhibitor (SHI-1:2) optimization. Bioorganic & Medicinal Chemistry Letters. 19: 1168-72. PMID 19138845 DOI: 10.1016/J.Bmcl.2008.12.083 |
0.102 |
|
1999 |
Berk SC, Rohrer SP, Degrado SJ, Birzin ET, Mosley RT, Hutchins SM, Pasternak A, Schaeffer JM, Underwood DJ, Chapman KT. A combinatorial approach toward the discovery of non-peptide, subtype-selective somatostatin receptor ligands. Journal of Combinatorial Chemistry. 1: 388-96. PMID 10748735 |
0.097 |
|
1997 |
Berk SC, Chapman KT. Spatially arrayed mixture (SpAM) technology: Synthesis of two-dimensionally indexed orthogonal combinatorial libraries Bioorganic and Medicinal Chemistry Letters. 7: 837-842. DOI: 10.1016/S0960-894X(97)00113-3 |
0.086 |
|
1998 |
Yang L, Berk SC, Rohrer SP, Mosley RT, Guo L, Underwood DJ, Arison BH, Birzin ET, Hayes EC, Mitra SW, Parmar RM, Cheng K, Wu TJ, Butler BS, Foor F, et al. Synthesis and biological activities of potent peptidomimetics selective for somatostatin receptor subtype 2. Proceedings of the National Academy of Sciences of the United States of America. 95: 10836-41. PMID 9724791 DOI: 10.1073/pnas.95.18.10836 |
0.082 |
|
1999 |
Rohrer SP, Berk SC. Development of somatostatin receptor subtype selective agonists through combinatorial chemistry. Current Opinion in Drug Discovery & Development. 2: 293-303. PMID 19649957 |
0.078 |
|
1998 |
Rohrer SP, Birzin ET, Mosley RT, Berk SC, Hutchins SM, Shen DM, Xiong Y, Hayes EC, Parmar RM, Foor F, Mitra SW, Degrado SJ, Shu M, Klopp JM, Cai SJ, et al. Rapid identification of subtype-selective agonists of the somatostatin receptor through combinatorial chemistry. Science (New York, N.Y.). 282: 737-40. PMID 9784130 DOI: 10.1126/science.282.5389.737 |
0.063 |
|
2010 |
Kaczmarek P, Singh V, Cashen DE, Yang L, Berk S, Pasternak A, Xiong Y, Shen DM, Hutchins SM, Chapman K, Wiedenmann B, Schaeffer JM, Strowski MZ. Somatostatin receptor subtypes 2 and 5 mediate inhibition of egg yolk-induced gall bladder emptying in mice. Neurogastroenterology and Motility : the Official Journal of the European Gastrointestinal Motility Society. 22: 204-9, e66. PMID 19754922 DOI: 10.1111/j.1365-2982.2009.01407.x |
0.055 |
|
2019 |
Akin D, Berk S, Sener Y, Kepenek A, Ozdas SB, Demircan G. Trigonelline's effect on BCL-2 protein expression level in THP-1 cells Journal of Biotechnology. 305: S24. DOI: 10.1016/j.jbiotec.2019.05.094 |
0.01 |
|
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