134307-35-0

Upstream product

• 134307-33-8 1-N,2-O,3-O,5-O-tetrabenzyl-4-O-mesyl-D-arabinonamide 
• 220939-94-6 (3S,4R)-1,3,4-tris(benzyloxy)-hex-5-en-2-one 
• 100-46-9 benzylamine 
• 260551-24-4 C₂₈H₃₄O₉S₂ 
• 160549-10-0 2,3,5-tri-O-benzyl-D-arabinofuranose 
• 14233-65-9 1-N,2-O,3-O,5-O-tetrabenzyl-D-arabinonamide 
• 14233-64-8 tri-O-benzyl-D-arabinolactone 
• 134502-24-2 2,3,5-tri-O-benzyl-D-arabinitol 1,4-sulfate 
• 134307-34-9 2,3,5-tri-O-benzyl-1-(benzylamino)-1-deoxy-D-arabitol 
• 124-63-0 methanesulfonyl chloride 

Relevant academic research and scientific papers

Microwave-assisted synthesis of pyrrolidine derivatives

Microwave-assisted bismesylate amination is an efficient method of synthesizing pyrrolidine ring derivatives and provides a good to excellent product yield.

Synthesis of naturally occurring iminosugars from d-fructose by the use of a zinc-mediated fragmentation reaction

A short synthesis of 1,4-dideoxy-1,4-imino-d-arabinitol (DAB) and a formal synthesis of australine are described. In both cases, d-fructose is employed as the starting material and converted into a protected methyl 6-deoxy-6-iodo- furanoside. Zinc-mediate

A cyclic sulfate approach to the synthesis of 1,4-dideoxy-1,4-imino derivatives of L-xylitol, L-arabinitol and D-xylitol

Polyhydroxylated pyrrolidines are readily accessible by ring opening of a 1,4-cyclic sulfate function in pentitol derivatives by nitrogen nucleophiles and further processing of the in situ generated charged sulfate group.