1007233-11-5Relevant academic research and scientific papers
Molecular iodine-catalyzed, one-pot, diastereoselective synthesis of 4-amido tetrahydropyrans
Sabitha, Gowravaram,Bhikshapathi,Nayak, Sambit,Yadav
, p. 8 - 15 (2011)
A simple and efficient one-pot synthesis of symmetrical 4-amido tetrahydropyrans via the Sakurai-Prins-Ritter reaction sequence using molecular iodine as catalyst from an aldehyde and allyltrimethylsilane in acetonitrile is described. This new method has
A Sakurai-Prins-Ritter reaction sequence for the diastereoselective synthesis of 4-amidotetrahydropyrans catalyzed by bismuth triflate
Sabitha, Gowravaram,Bhikshapathi,Nayak, Sambit,Yadav,Ravi,Kunwar
, p. 5727 - 5731 (2008/12/22)
The synthesis of 4-amidotetrahydropyrans has been achieved by a single-step Sakurai-Prins-Ritter reaction sequence in a domino fashion by the reaction of an aldehyde and allyltrimethylsilane in acetonitrile using Bi(OTf)3 as catalyst. The prese
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.
