Synthesis of spirofuranopyrimidine–piperidines
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference19 articles.
1. Aryl urea derivatives of spiropiperidines as NPY Y5 receptor antagonists
2. Discovery of potent, selective, and orally bioavailable 3H-spiro[isobenzofuran-1,4′-piperidine] based melanocortin subtype-4 receptor agonists
3. Peptidomimetic Growth Hormone Secretagogues. Design Considerations and Therapeutic Potential
4. Preparation of 3,4-fused-spiro[furan-5(5H),4′-piperidin]-2-one
5. Design and biological activities of L-163,191 (MK-0677): a potent, orally active growth hormone secretagogue.
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1. Synthesis, characterization, DNA interaction, molecular docking, and α-amylase and α-glucosidase inhibition studies of a water soluble Zn(ii) phthalocyanine;Dalton Transactions;2024
2. Synthetic approaches toward piperidine related structures: A review;Synthetic Communications;2020-06-16
3. Intramolecular Cycloaddition of Azomethine Ylides Activated by Aromatic Rings: Scope and Limitations;Chemistry of Heterocyclic Compounds;2016-07
4. ChemInform Abstract: Synthesis of Spirofuranopyrimidine-Piperidines.;ChemInform;2012-09-20
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