Patrick Stoy, Ph.D.

Affiliations: 
2004 University of Michigan, Ann Arbor, Ann Arbor, MI 
Area:
synthetic organic chemistry with a focus on the area of heterocyclic chemistry
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"Patrick Stoy"

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William H. Pearson grad student 2004 University of Michigan
 (I. Completion of the synthesis of Kopsia lapidilecta alkaloid (+/-)-lapidilectine B. II. Synthesis of 1-azabicyclo[n.3.0]alkanes via [3+2] cycloadditions of nonstabilized azomethine ylides.)
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Publications

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Pearson WH, Berry DA, Stoy P, et al. (2005) Fluorous affinity purification of oligonucleotides. The Journal of Organic Chemistry. 70: 7114-22
Pearson WH, Lee IY, Mi Y, et al. (2005) Total Synthesis of the Kopsia lapidilecta Alkaloid (.+-.)-Lapidilectine B (I). Cheminform. 36
Pearson WH, Lee IY, Mi Y, et al. (2004) Total synthesis of the Kopsia lapidilecta alkaloid (+/-)-lapidilectine B. The Journal of Organic Chemistry. 69: 9109-22
Pearson WH, Stoy P, Mi Y. (2004) A three-component, one-pot synthesis of indolizidines and related heterocycles via the [3+2] cycloaddition of nonstabilized azomethine ylides. The Journal of Organic Chemistry. 69: 1919-39
Pearson WH, Dietz A, Stoy P. (2004) Azomethine ylides from tin-substituted cyclic carbinol amides: a new route to highly substituted pyrrolizidines. Organic Letters. 6: 1005-8
Bi Y, Stoy P, Adam L, et al. (2004) Quinolines as extremely potent and selective PDE5 inhibitors as potential agents for treatment of erectile dysfunction. Bioorganic & Medicinal Chemistry Letters. 14: 1577-80
Stoy P, Rush J, Pearson WH. (2004) The synthesis of 9,10-dihydro-9-,10-(methaniminomethano)anthracene and N-protected derivatives via double reductive amination Synthetic Communications. 34: 3481-3489
Pearson WH, Stoy P. (2003) Cycloadditions of nonstabilized 2-azaallyllithiums (2-azaallyl anions) and azomethine ylides with alkenes: [3+2] Approaches to pyrrolidines and application to alkaloid total synthesis Synlett. 903-921
Pearson WH, Mi Y, Lee IY, et al. (2001) Total synthesis of the Kopsia lapidilecta alkaloid (+/-)-lapidilectine B. Journal of the American Chemical Society. 123: 6724-5
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