119770-85-3

Upstream product

• 867-13-0 diethoxyphosphoryl-acetic acid ethyl ester 
• 76227-09-3 (R)-2-benzyloxy-3-hydroxy-propionaldehyde 
• 131771-68-1 1-(phenylsulfonyl)-3,4-di-O-benzyl-D-xylal 
• 84379-52-2 (2R,3R)-3-(benzyloxy)butane-1,2,4-triol 
• 100-52-7 benzaldehyde 
• 32780-06-6 (5S)-5-(hydroxymethyl)-2-oxo-tetrahydrofuran 
• 133328-91-3 (S)-5-Benzyloxy-tetrahydro-pyran-2-one 
• 187264-97-7 (5S)-5-(((tetrahydro-2H-pyran-2-yl)oxy)methyl)dihydrofuran-2(3H)-one 
• 133328-90-2 (S)-4-Hydroxy-5-(tetrahydro-pyran-2-yloxy)-pentanoic acid dimethylamide 
• 131771-62-5 (2R,3R,4S,5R)-3,4,5-Tris-benzyloxy-2-phenylsulfanyl-tetrahydro-pyran 
• 131771-66-9 phenyl 2,3,4-tri-O-benzyl-1-thio-β-D-xylopyranoside 
• 131771-67-0 (2S,3R,4S,5R)-2-Benzenesulfonyl-3,4,5-tris-benzyloxy-tetrahydro-pyran 
• 131771-63-6 (2R,3R,4S,5R)-2-Benzenesulfonyl-3,4,5-tris-benzyloxy-tetrahydro-pyran 

Downstream Products

• 133328-93-5 (4R,5S)-5-Benzyloxy-4-propyl-tetrahydro-pyran-2-one 
• 133328-94-6 (4S,5S)-5-Benzyloxy-4-propyl-tetrahydro-pyran-2-one 
• 133328-96-8 (4R,5S)-5-Benzyloxy-4-butyl-tetrahydro-pyran-2-one 

Relevant academic research and scientific papers

A Convenient Synthesis of Pyranoid Ene Lactones from Phenyl Glycosyl Sulfones

O-Benzyl protected pyranoid ene lactones (5,6-dihydro-2H-pyran-2-ones) 4a-c, 8 were obtained in high yield in a two-step procedure.Treatment of the phenyl glycosyl sulfones 2a-d, 6, which were readily prepared from their corresponding sulfides, with lithi

Conjugate addition to chiral γ-heterosubstituted δ-lactones as pivotal synthons from L-glutamic acid. Synthesis of an optically active lignan lactone; (-)-hinokinin

Asymmetric induction in conjugate addition of new chiral γ-heterosubstituted-α, β-unsaturated δ-lactones from L-glutamic acid was accomplished in high diastereoselectivity with the formation of trans-(R,S)-adducts and was disclosed to serve as a versatile procedure for the asymmetric synthesis of antileukemic lignan lactones.