1007233-16-0Relevant articles and documents
Three-component, one-pot diastereoselective synthesis of 4-amidotetrahydropyrans via the Prins-Ritter reaction sequence
Yadav,Reddy, B.V. Subba,Aravind,Kumar, G.G.K.S. Narayana,Madhavi,Kunwar
, p. 3025 - 3031 (2008)
Three-component coupling of carbonyl compounds, homoallylic alcohols, and nitriles has been achieved using 20 mol % of phosphomolybdic acid (PMA) at ambient temperature via the Prins-Ritter sequence to furnish 4-amidotetrahydropyrans in high yields with a
Stereoselective one-pot, three-component synthesis of 4- amidotetrahydropyran
Reddy,Rama Raju,Pramod Kumar,Saikia, Anil K.
, p. 1628 - 1630 (2008/09/17)
(Chemical Equation Presented) The reaction of aldehyde with allylsilane in acetonitrile mediated by boron trifluoride etherate generated 4-aminotetrahydropyrans in good yields. The product is highly stereoselective.