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Jeffrey M. Dener - Publications

Affiliations: 
Chemistry Ohio State University, Columbus, Columbus, OH 
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7 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
2004 Kane TR, Ly CQ, Kelly DE, Dener JM. Solid-phase synthesis of 1,2,3,4-tetrahydroisoquinoline derivatives employing support-bound tyrosine esters in the Pictet-Spengler reaction. Journal of Combinatorial Chemistry. 6: 564-72. PMID 15244418 DOI: 10.1021/cc020105t  0.326
2004 Bunin BA, Dener JM, Kelly DE, Paras NA, Tario JD, Tushup SP. Solid-phase synthesis of 1-substituted tetrahydroisoquinoline derivatives employing BOC-protected tetrahydroisoquinoline carboxylic acids. Journal of Combinatorial Chemistry. 6: 487-96. PMID 15244409 DOI: 10.1021/Cc0340776  0.35
2001 Dener JM, Lease TG, Novack AR, Plunkett MJ, Hocker MD, Fantauzzi PP. Solid-phase synthesis of 2,4-diaminoquinazoline libraries. Journal of Combinatorial Chemistry. 3: 590-7. PMID 11703156 DOI: 10.1021/cc010027u  0.338
1999 Bunin BA, Dener JM, Livingston DA. Chapter 27. Application of Combinatorial and Parallel Synthesis to Medicinal Chemistry Annual Reports in Medicinal Chemistry. 34: 267-286. DOI: 10.1016/S0065-7743(08)60589-8  0.349
1988 Dener JM, Hart DJ, Ramesh S. .alpha.-Acylamino radical cyclizations: application to the synthesis of (-)-swainsonine The Journal of Organic Chemistry. 53: 6022-6030. DOI: 10.1021/Jo00261A007  0.398
1988 Dener JM, Hart DJ. α-Acylamino radical cyclizations using allenes and vinylsilanes as addends: applications to the synthesis of (+)-heliotridine and (-)-dihydroxyheliotridine Tetrahedron. 44: 7037-7046. DOI: 10.1016/S0040-4020(01)86072-5  0.477
1988 Dener JM, Hart DJ, Ramesh S. α-Acylamino radical cyclizations: Application to the synthesis of (-)-swainsonine Journal of Organic Chemistry. 53: 6022-6030.  0.52
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