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John A. Wendt

Pfizer

12

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312

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Synthesis and SAR of 2-aryl pyrido[2,3-d]pyrimidines as potent mGlu5 receptor antagonists.

2007 Bioorganic & Medicinal Chemistry Letters
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Synthesis and SAR comparison of regioisomeric aryl naphthyridines as potent mGlu5 receptor antagonists

2007 Bioorganic & Medicinal Chemistry Letters
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Rational design of 7-arylquinolines as non-competitive metabotropic glutamate receptor subtype 5 antagonists

2007 Bioorganic & Medicinal Chemistry Letters
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Synthesis and SAR of 2-aryl pyrido[2,3-d]pyrimidines as potent mGlu5 receptor antagonists.

2007 Bioorganic & Medicinal Chemistry Letters
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Convergent, parallel synthesis of a series of β-substituted 1,2,4-oxadiazole butanoic acids as potent and selective αvβ3 receptor antagonists

2006 Bioorganic & Medicinal Chemistry Letters
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Synthesis of 2,5-thiazole butanoic acids as potent and selective αvβ3 integrin receptor antagonists with improved oral pharmacokinetic properties

2006 Bioorganic & Medicinal Chemistry Letters
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First Asymmetric Total Synthesis of (+)-Sparteine

2002 Organic Letters
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Toward the synthesis of sparteine: Intramolecular Schmidt reactions on a norbornanone platform

1996 Tetrahedron Letters
- John A. Wendt
- Jeffrey Aubé
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SYNTHESIS OF ()-FREDERICAMYCIN A

1994 Journal of the American Chemical Society
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