Stereoselective Synthesis of Hexahydro‑1<i>H</i>‑spiro[isoquinoline-4,4′-pyran] Scaffolds through an Intramolecular Prins Cascade Process
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A novel tandem cyclization strategy has been developed for the synthesis of hexahydro-1H-spiro[isoquinoline-4,4′-pyran] derivatives through the condensation of 3-((benzylamino)methyl)but-3-en-1-ol with aldehydes using BF3·OEt2. The reaction proceeds in a highly stereoselective manner, leading to a single diastereoisomer. This approach is a simple and efficient alternative for the synthesis of pharmacologically important spiroisoquinoline scaffolds.
创建时间:
2015-01-02



