157604-63-2Relevant academic research and scientific papers
A new etherification reaction in the η4-dienyl-tricarbonyliron series: Access to the 2,5-disubstituted-1,4-dioxane core
Lellouche,Quirosa-Guillou
, p. 977 - 993 (1995)
The η4-dienyl tricarbonyliron complex 8 has been used as a valuable building block en route to the 2,5-disubstituted-1,4-dioxane 4. Particularly noteful is the new regioselective etherification reaction of 8 with the suitably protected secondary glycerol 11 through the non-isolated organometallic cation 13.
Chiral Lactols, XI. - A Method for the Determination of the Absolute Configuration of Chiral Alkanols
Noe, Christian R.,Knollmueller, Max,Miculka, Christian,Dungler, Karin,Wagner, Ernst,Ettmayer, Peter
, p. 887 - 892 (2007/10/02)
Chiral secondary alcohols which are protected with the enantiomerically pure lactol 1 or 2 show significant differences in 13C-chemical shifts around the glycosidic linkage.An easy method for determination of the absolute configuration of secondary alcoho
