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Kenneth Jay Barr - Publications

Affiliations: 
Forma Therapeutics, Watertown, MA 
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8 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 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  0.706
2010 BARR KJ, WATSON BT, BUCHWALD SL. ChemInform Abstract: Zirconocene(iso-butyl) Chloride: In situ Generation of a Zirconocene( methyl) Chloride Equivalent for Use in Organic Synthesis. Cheminform. 23: no-no. DOI: 10.1002/chin.199225234  0.666
1999 Martin SF, Barr KJ, Smith DW, Bur SK. Applications of vinylogous Mannich reactions. Concise enantiospecific total syntheses of (+)-croomine Journal of the American Chemical Society. 121: 6990-6997. DOI: 10.1021/Ja990077R  0.428
1996 Martin SF, Barr KJ. Vinylogous Mannich reactions. The asymmetric total synthesis of (+)-croomine Journal of the American Chemical Society. 118: 3299-3300. DOI: 10.1021/Ja9542146  0.313
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  0.687
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.  0.72
1992 Gupton JT, Krolikowski DA, Yu RH, Barr KJ, Duranceau SJ. New reactions of quaternary ammonium salts derived from vinamidinium salt reduction products and a reassignment of structure Synthetic Communications. 22: 1067-1076. DOI: 10.1080/00397919208019298  0.321
1991 Barr KJ, Watson BT, Buchwald SL. Zirconocene(iso-butyl) chloride: In situ generation of a zirconocene(methyl) chloride equivalent for use in organic synthesis Tetrahedron Letters. 32: 5465-5468. DOI: 10.1016/0040-4039(91)80059-F  0.664
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