31518-17-9Relevant academic research and scientific papers
Enolate Free α-Alkoxyvinyllithium Reagents: Improved Preparetion and Reaction with N,N-Dialkylcarboxamides
Shimano, Masanao,Meyers, A. I.
, p. 7727 - 7730 (1994)
The titled lithium reagents add to a variety of N,N-dialkylcarboxamides furnishing the enol ethers of α-dicarbonyl compounds.
Triol protection with 6-benzoyl-3,4-dihydro-(2H)-pyran
Baker, Caroline D. L.,Fawcett, John,Insley, Christopher D.,Messenger, Derek S.,Newland, Claire L.,Overend, Helen L.,Patel, Anup B.,Shah, Mufakhrul,Vara, Bhavna,Virdee, Davinder,Rawlings, Bernard J.
, p. 1883 - 1885 (2005)
6-Benzoyl-3,4-dihydro-(2H)-pyran will protect 1,2,3-triols such as glycerol as their corresponding spiro-[5-phenyl-3,6,8-trioxabicyclo[3.2.1]octane-4, 2′-tetrahydropyran]s and 1,2,4-triols (less efficiently) as the corresponding trioxabicyclo[3.2.2]nonane
