1513847-27-2

Upstream product

• 53270-14-7 benzyl 2,3-O-isopropylidene-α-L-rhamnopyranoside 
• 1513847-25-0 C₂₂H₂₈O₇ 
• 865484-73-7 tert-butyl ((2S,6S)-6-methyl-5-oxo-5,6-dihydro-2H-pyran-2-yl) carbonate 

Downstream Products

• 1513847-31-8 C₂₅H₃₁ClO₉ 
• 1513847-33-0 1-benzyl 2,3-didehydro-α-L-rhamnopyranosyl-(1→4)-2-O-chloroacetyl-3-O-isobutyryl-α-L-rhamnopyranoside 
• 1513847-34-1 1-benzyl 2,3-didehydro-4-O-isobutyryl-α-L-rhamnopyranosyl-(1→4)-2-O-chloroacetyl-3-O-isobutyryl-α-L-rhamnopyranoside 
• 1513847-38-5 1-benzyl 4-O-isobutyryl-α-L-rhamnopyranosyl-(1→4)-2-O-chloroacetyl-3-O-isobutyryl-α-L-rhamnopyranoside 
• 1513847-39-6 1-benzyl 4-O-isobutyryl-2,3-O-isopropylidene-α-L-rhamnopyranosyl-(1→4)-2-O-chloroacetyl-3-O-isobutyryl-α-L-rhamnopyranoside 
• 1513847-29-4 C₂₃H₃₀O₈ 

Relevant academic research and scientific papers

Merremoside D: De novo synthesis of the purported structure, nmr analysis, and comparison of spectral data

The first synthesis of the purported structure of Merremoside D has been achieved in 22 longest linear steps. The de novo asymmetric synthesis relied on the use of asymmetric catalysis to selectively install all 21 stereocenters in the final compounds fro