946051-14-5Relevant articles and documents
Iodine/accl-catalyzed prins-ritter reaction: Synthesis of 4-amido tetrahydropyrans
Srinivasan,Perumal,Raja
experimental part, p. 1083 - 1091 (2011/10/01)
Homoallylic alcohols, carbonyl compounds and nitriles undergo a smooth tandem Prins-Ritter type cyclization in the presence of iodine/AcCl at room temperature to produce 4-acetamido tetrahydropyrans in high yields with all cis-selectivity.
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 (2008/09/19)
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
CeCl3·7H2O/AcCl-catalyzed Prins-Ritter reaction sequence: a novel synthesis of 4-amido tetrahydropyran derivatives
Yadav,Reddy, B.V. Subba,Kumar, G.G.K.S. Narayana,Reddy, G. Madhusudhan
, p. 4903 - 4906 (2008/02/08)
Homoallylic alcohols, carbonyl compounds and nitriles undergo a smooth tandem Prins-Ritter type cyclization in the presence of CeCl3·7H2O/AcCl at ambient temperature to produce 4-amido tetrahydropyrans in high yields with all cis-sel