958643-54-4

Upstream product

• 3162-96-7 methyl-4,6-O-phenylmethylene-α-D-mannopyranoside 
• 617-04-9 (2R,3S,4S,5S,6S)-2-(hydroxymethyl)-6-methoxytetrahydro-2H-pyran-3,4,5-triol 
• 7177-79-9 methyl 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside 
• 6988-40-5 methyl 2,3-di-O-benzyl-α-D-mannopyranoside 

Downstream Products

• 1064180-84-2 C₂₀H₂₄O₄ 
• 155049-46-0 methyl 2,3,4-tri-O-benzyl-5-methylene-α-D-lyxopyranoside 
• 127545-53-3 (4R,5R,6S)-4,5,6-trihydroxy-2-methyl-2-cyclohexen-1-one 
• 1313193-62-2 C₂₁H₂₄O₅ 
• 1313193-71-3 C₂₃H₂₄O₆ 
• 1313193-69-9 C₂₂H₂₂O₅ 
• 1313193-68-8 C₂₃H₂₆O₆ 
• 1313193-66-6 (4R,5R,6S)-4,5,6-tris(benzyloxy)-2-methylcyclohex-2-enone 
• 1313193-65-5 (4R,5R,6S)-4,5,6-tris(benzyloxy)-2-iodocyclohex-2-en-1-one 
• 155155-66-1 C₂₇H₂₆O₄ 

Relevant academic research and scientific papers

An iodocyclization approach toward diastereoselective synthesis of highly functionalized tetrasubstituted tetrahydrofurans with 2,5-trans and 2,5-cis relationships from pyranoside derived acyclic oximes

An efficient method to obtain novel tetrasubstituted tetrahydrofurans with C2 and C5 substitution in trans- and cis-relative configurations has been reported.