| Literature DB >> 28561323 |
Samuel D Griggs1, Nathan Thompson1, Daniel T Tape2, Marie Fabre1, Paul A Clarke1.
Abstract
A general two-step synthesis of 2-spiropiperidines has been developed. δ-Amino-β-ketoesters can be reacted with cyclic ketones to generate 2-spiropiperidines in good to excellent yields. The 2-spiropiperidines formed occupy an under-explored region of 3D-chemical space and are novel scaffolds for use in drug discovery programs. These 2-spiropiperidines can be further functionalised to generate small highly sp3 -rich structures, which exhibit an excellent likeness to lead-molecules in drug discovery.Entities:
Keywords: Maitland-Japp; medicinal chemistry; piperidine; scaffolds; spirocyclic
Year: 2017 PMID: 28561323 DOI: 10.1002/chem.201702467
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236