118495-40-2

Upstream product

• 133437-07-7 (2R,3R,4S)-5-Benzylamino-2,3,4-tris-benzyloxy-pentan-1-ol 
• 98243-24-4 L-ido-BrHg(C₃₄H₃₆NO₃) 
• 100-46-9 benzylamine 

Downstream Products

• 129611-25-2 (3α,4β,5α)-tris(phenylmethoxy)piperidine 
• 13042-55-2 (3R,5R)-piperidine-3,4,5-triol 

Relevant academic research and scientific papers

HYDROXYLATED PIPERIDINES: SYNTHESIS OF 1,5-ALKYLIMINO-1,5-DIDEOXY DERIVATIVES OF XYLITOL, D- AND L-ARABINITOL, AND RIBITOL

Direct routes are reported for the synthesis of N-propyl, N-butyl and N-pentyl-1,5-dideoxy-1,5-iminoxylitol (7a,b,c), the analogous derivatives (8a,b,c, and 9a,b,c) of 1,5-dideoxy-1,5-imino-D- and -L-arabinitol, and of N-propyl-1,5-dideoxy-1,5-iminoribito

The use of triphenylphosphine/diethyl azodicarboxylate (DEAD) for the cyclization of 1,4- and 1,5-amino alcohols

Application of the Mitsunobu reagent to the cyclization of 1,4- and 1,5-amino alcohols provided an assortment of azacycles in good to excellent yield.

A new family of five-carbon iminoalditols which are potent glycosidase inhibitors

The synthesis of 1,5-dideoxy-1,5-imino-D-xylitol 2 (and the enantiomeric iminoalditols 3 and 4) is described. Alditol 2 compares favorably with 1-deoxynojirimycin 1 as a potent inhibitor of β-glucosidase.