78508-99-3

Upstream product

• 110-00-9 furan 
• 78508-98-2 lithium (2S,3R)-2,3-(N,O-benzylidyne)-2-amino-3-hydroxy-butyrate 
• 60538-17-2 (4R,5R)-4-(methoxycarbonyl)-5-methyl-2-phenyl-Δ²-oxazoline 

Downstream Products

• 78509-01-0 (1S,2S,3R)-2,3-(N,O-benzylidyne)-2-amino-1-(2-furyl)-1,3-butandiol 
• 78509-01-0 (1R,2S,3R)-2,3-(N,O-benzylidyne)-2-amino-1-(2-furyl)-1,3-butandiol 
• 78549-27-6 (1S,2S,3R)-2-(N-benzoylamino)-1-(2-furyl)-1,3-butandiol 
• 78509-03-2 (1R,2S,3R)-2-(N-benzoylamino)-1-(2-furyl)-1,3-butandiol 
• 78548-86-4 (1S,2S,3R)-1,3-O-isopropylidene-2-(N-benzoylamino)-1,3-butandiol 
• 78509-04-3 (1R,2S,3R)-1,3-O-isopropylidene-2-(N-benzoylamino)-1,3-butandiol 

Relevant academic research and scientific papers

SYNTHESIS AND ABSOLUTE CONFIGURATION OF TWO DIASTEREOISOMERIC (1R,2S,3R)-AND (1S,2S,3R)-2-AMINO-1-(2-FURYL)-1,3-BUTANDIOLS

The synthesis of (1R,2S,3R)-and (1S,2S,3R)-2-(N-benzoylamino)-1-(2-furyl)-1,3-butandiols (15) and (16) from D-threonine is described.The assignment of absolute configuration of the newly formed asymmetric center at C-1 was based on the (1)H-NMR spectra of