127940-38-9Relevant academic research and scientific papers
SYNTHESIS OF ENANTIOMERICALLY PURE 2,3-DIDEOXY-HEPT-2-ENONO-1,4-LACTONE DERIVATIVES VIA DIASTEREOSELECTIVE ADDITION OF 2-(TRIMETHYLSILOXY)FURAN TO D-GLYCERALDEHYDE AND D-SERINAL-BASED THREE-CARBON SYNTHONS
Casiraghi, Giovanni,Colombo, Lino,Rassu, Gloria,Spanu, Pietro
, p. 5325 - 5328 (2007/10/02)
The BF3-promoted addition of 2-(trimethylsiloxy)furan to 2,3-O-isopropylidene-D-glyceraldehyde and N-t-BOC-D-serinal, and the corresponding imine derivatives gives the title seven-carbon lactones with great preference for the D-arabino diastereoisomers.
