89755-55-5

Upstream product

• 1530-32-1 ethyltriphenylphosphonium bromide 
• 23558-05-6 3-O-benzyl-1,2-O-isopropylidene-1,5-D-xylo-dialdofuranose 
• 100-39-0 benzyl bromide 
• 18685-18-2 3-O-benzyl-1,2-5,6-O-diisopropylidene-α-D-glucofuranose 
• 22331-21-1 1,2:5,6-di-O-isopropylidene-3-O-benzyl-α-D-allofuranose 
• 14686-89-6 (1,2:5,6)-di-O-isopropylidene-D-gulose 

Downstream Products

• 131087-27-9 (2S,3S,4R)-1,2-Cyclopentylidenedioxy-3,4-dibenzyloxyheptane 
• 131087-26-8 (2S,3S,4R)-3-Benzyloxy-1,2-cyclopentylidenedioxy-4-hydroxyheptane 
• 131087-25-7 (2S,3S,4R)-3-Benzyloxy-1,2,4-trihydroxyheptane 
• 131087-27-9 (2S,3R,4R)-1,2-Cyclopentylidendioxy-3,4-dibenzyloxyheptane 
• 131087-25-7 (2S,3R,4R)-3-Benzyloxy-1,2,4-trihydroxyheptane 
• 146072-02-8 3-O-Benzyl-5-deoxy-5-C-ethyl-1,2-O-isopropylidene-α-D-ribofuranose 
• 89755-50-0 1,2-O-Isopropylidene-3-O-benzyl-5-deoxy-5-C-ethyl-α-D-xylofuranose 

Relevant academic research and scientific papers

Stereoselective Synthesis of Unnatural Stereoisomers of LL-P880β and LL-P880γ, Pestatolin Analogues from Penicillium sp.

A synthesis of unnatural stereoisomers of LL-P880β and (2) and subsequent transformation of 2 into LL-P880γ (3) were achieved by starting from diacetoneglucose (4).A chiral building block, 5-deoxy-α-D-ribofuranose derivative 9, was derived from 4 by two s

Total Synthesis of (6S,1'S,2'R)-6-(1',2'-Dihydroxypentyl)-4-methoxy-5,6-dihydropyrane-2-one (LL-P880β) and Its C6-Epimer, a Fungal Metabolite from Penicillium sp.

A fungal metabolite, (6S,1'S,2'R)-6-(1',2'-dihydroxypentyl)-4-methoxy-5,6-dihydropyrane-2-one (LL-P880β, I), and its C6-epimer (II) were synthesized by the chiron approach.The key intermediate, (2S,3R)-2,3-dihydroxyhexanal derivative (3), was p