694503-79-2Relevant academic research and scientific papers
Diastereoselective dihydroxylation and regioselective deoxygenation of dihydropyranones: A novel protocol for the stereoselective synthesis of C 1-C8 and C15-C21 subunits of (+)-discodermolide
Ramachandran, P. Veeraraghavan,Prabhudas, Bodhuri,Chandra, J. Subash,Reddy, M. Venkat Ram
, p. 6294 - 6304 (2007/10/03)
Diastereoselective dihydroxylation of dihydropyranones and subsequent regioselective α-deoxygenation provides 1,3-trans-β-hydroxy-6- lactones stereoselectively. This protocol has been applied for the synthesis of C1-C8 and C15-C21 subunits of (+)-discodermolide.
Asymmetric synthesis of 6-(2′,3′,4′,5′, 6′-pentafluorophenyl)-δ-lactones via "allyl"boranes via "allyl" boranes: Application for the synthesis of fluorinated analog of key pharmacophore of statin drugs
Ramachandran, P. Veeraraghavan,Padiya, Kamlesh J.,Rauniyar, Vivek,Reddy, M. Venkat Ram,Brown, Herbert C.
, p. 615 - 620 (2007/10/03)
Asymmetric "allyl"boration of pentafluorobenzaldehyde with various α-pinene based "allyl"boranes provides homoallylic alcohols in high de and ee; the alcohols have been converted into δ-lactones via acryloylation, ring-closing metathesis and hydrogenation
