124315-89-5Relevant academic research and scientific papers
STEREOSELECTIVE SYNTHESIS OF HYDROXY-SUBSTITUTED TETRAHYDROFURANS
Kim, Young Gyu,Cha, Jin K.
, p. 2011 - 2014 (1988)
Iodocyclizations of 4-alkene-1,3-diol derivatives proceed with high stereocontrol to provide cis 2-iodomethyl-3-hydroxy(alkoxy)tetrahydrofurans.The effect of alkoxy substituents on the diastereoselectivity has also been assessed.
HIGHLY STEREOSELECTIVE SYNTHESIS OF DI- AND TRISUBSTITUTED HOMOALLYLIC ALCOHOLS VIA PALLADIUM(O)-CATALYZED NUCLEOPHILIC OPENING OF VINYLIC OXETANES
Larock, Richard C.,Stolz-Dunn, Sandra K.
, p. 3487 - 3490 (2007/10/02)
Vinylic oxetanes react in an SN2' manner with a variety of potential nucleophiles in the presence of catalytic amounts of Pd(PPh3)4 to afford the corresponding highly functionalized, di- and trisubstituted homoallylic alcohols with high stereos
