Synthesis of a Spiro[cyclohex-1,1‘-isobenzofuranyl] Dopamine Receptor Antagonist
Author:
Affiliation:
1. Pfizer Inc, Central Research Division, Process Research and Development Department, Eastern Point Rd., Groton, Connecticut, 06340, U.S.A.
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/op990191u
Reference8 articles.
1. Current address: Ilex Oncology, 14785 Omicron Drive, # 101, San Antonio, TX 78245-3221.
2. Regioselective nucleophilic substitutions of fluorobenzene derivatives
3. Homogeneous hydrogen-transfer reactions catalyzed by tricarbonyl chromium complexes. Hydrogenation of trienes
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2. Discovery and evaluation of spirocyclic derivatives as antagonists of the neuropeptide Y5 receptor;Bioorganic & Medicinal Chemistry Letters;2012-04
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4. Practical Synthesis of (1s,4s)-4-(Methylamino)-1′H-spiro[cyclohexane-1,3′-furo[3,4-c]pyridin]-1′-one;Organic Process Research & Development;2010-07-21
5. ChemInform Abstract: Synthesis of a Spiro[cyclohex-1,1′-isobenzofuranyl] Dopamine Receptor Antagonist.;ChemInform;2010-06-10
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