27 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

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 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
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
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
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