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Solid-phase Synthesis of [4.4] Spirocyclic Oximes
Published on: February 6, 2019
Spirocyclic nonpeptide glycoprotein IIb-IIIa antagonists. Part 3: synthesis and SAR of potent and specific
Mukund M Mehrotra1, Julie A Heath, Jack W Rose
1COR Therapeutics, Inc., Department of Medicinal Chemistry, South San Francisco, CA 94080, USA.
Bioorganic & Medicinal Chemistry Letters
|March 23, 2002
Abstract:
The synthesis and biological activity of analogues containing spiro piperidinylpyridine and pyrrolidinylpyridine templates are described. The potent activity of these compounds as platelet aggregation inhibitors demonstrates the utility of the spiro structures as central template for nonpeptide RGD mimics.
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