141468-41-9Relevant academic research and scientific papers
Synthesis of Bis-γ-Butyrolactones Containing Conformationally Constrained (S)- and (R)-Diacylglycerol Structures
Lee, Jeewoo,Lewin, Nancy E.,Blumberg, Peter M.,Marquez, Victor E.
, p. 1299 - 1306 (2007/10/03)
The synthesis of two sets of rigid diacylglycerol (DAG) analogues with either the (S)-DAG or (R)-DAG enantiomer embedded into a bis-γ-butyrolactone template was accomplished stereoselectively from di-O-isopropylidene-α-D-apiose.The key step in both synthe
Synthesis of two rigid diacylglycerol analogues having a bis-butyrolactone skeleton
Lee, Jeewoo,Teng, Kelly,Marquez, Victor E.
, p. 1539 - 1542 (2007/10/02)
The stereoselective synthesis of two rigid diacylglycerol analogues starting from protected D-apio-L-furanose (apiose) is described. The construction of the desired bis-butyrolactone bicyclic structure was accomplished via an intramolecular radical cycliz
