539836-41-4

Upstream product

• 862380-24-3 6-(2-pyridin-2-yl-ethyl)-pyridine-2-carboxylic acid methyl ester 
• 4294-57-9 para-methylphenylmagnesium bromide 
• 109-06-8 α-picoline 
• 1945-84-2 2-ethynylpyridine 
• 5453-67-8 2,6-bis(methoxycarbonyl)pyridine 
• 539836-34-5 1-[6-(hydroxy-di-p-tolyl-methyl)-pyridin-2-yl]-2-pyridin-2-yl-ethanol 
• 539836-30-1 1-[6-(hydroxy-di-p-tolyl-methyl)-pyridin-2-yl]-2-pyridin-2-yl-ethanol 
• 539836-27-6 6-(hydroxy-di-p-tolyl-methyl)-pyridine-2-carboxylic acid methyl ester 
• 862380-23-2 6-pyridin-2-yl-ethynyl-pyridine-2-carboxylic acid methyl ester 
• 539836-38-9 [6-(2-pyridin-2-yl-vinyl)-pyridin-2-yl]-di-p-tolyl-methanol 

Downstream Products

• 539836-43-6 methyl 6-O-[6-(2-pyridin-2-yl-ethyl)-pyridin-2-yl]-di-p-tolyl-methyl-α-D-glucopyranoside 

Relevant academic research and scientific papers

Directing-protecting groups for carbohydrates. Design, conformational study, synthesis and application to regioselective functionalization

A novel concept of regioselective transformation of secondary hydroxyl groups in carbohydrates is presented. First, the relative reactivity of the free hydroxyl groups of onoprotected d-glucose derivatives was assessed using acetylation as a model reactio

Modulation of the relative reactivities of carbohydrate secondary hydroxyl groups. Modification of the hydrogen bond network

An approach towards the control of the relative regioselectivity of the secondary hydroxyl groups is presented. Original protecting groups, which are capable of specific intramolecular hydrogen bonds and are likely to modulate the partial charges of the o