838838-37-2

Upstream product

• 838838-31-6 methyl α-D-4,6-O-((R)-benzylidene)-3-deoxy-3-(2-oxoethyl)-glucopyranosid-2-ulose 
• 135700-48-0 methyl 4,6-O-benzylidene-3-deoxy-3-C-propenyl-α-D-arabino-hexopyranoside-2-ulose 
• 838838-30-5 (2R,4aR,6S,8S,8aS)-6-Methoxy-2-phenyl-8-[1,2,4]trioxolan-3-ylmethyl-tetrahydro-pyrano[3,2-d][1,3]dioxin-7-one 

Downstream Products

• 1168136-52-4 methyl α-D-2-amino-4,6-O-((R)-benzylidene)-2,3-dideoxy-2-N,3-C-(ethane-1,2-diyl)-mannopyranoside 

Relevant academic research and scientific papers

Stereoselective synthesis by double reductive amination ring closure of novel aza-heteroannulated sugars

We present here the stereoselective synthesis of a series of 2/3-N-pyrrolidine derivatives of glycosides produced by diastereoselective double reductive amination ring closure of 1,4-dicarbonyl compounds. These precursors were produced by tandem ozonolysi

Ring-closing double reductive amination route to aza-heteroannulated sugars

1,4-Dicarbonyl derivatives of glycosides are produced by ozonolysis or Wacker oxidation. A stable ozonide is isolated and a carbonyl group reduced whilst maintaining the ozonide functionality. The 1,4-dicarbonyl compounds are converted to various N-substi