Title
Electrophile-induced ether transfer: An expedient route to 2-cyano-tetrahydropyrans
Document Type
Article
Publication Date
12-31-2007
Abstract
Electrophile-induced ether transfer reactions of alkoxymethyl ether protected homoallylic alcohols with cyanide quench provide cyanoether adducts in high yield and excellent 1,3-syn-stereoselectivity. Subsequent base-mediated cyclization then provides the corresponding 2,4,6-trisubstituted cyano-tetrahydropyran. © 2007 The Japan Institute of Heterocyclic Chemistry.
Publication Source (Journal or Book title)
Heterocycles
First Page
447
Last Page
459
Recommended Citation
Kartika, R., & Taylor, R. (2007). Electrophile-induced ether transfer: An expedient route to 2-cyano-tetrahydropyrans. Heterocycles, 74 (C), 447-459. Retrieved from https://repository.lsu.edu/chemistry_pubs/583
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