181935-92-2

Upstream product

• 2746-25-0 p-Methoxybenzyl bromide 
• 181933-87-9 2-(3'-dimethoxymethyl)phenyl-ethan-2-ol 

Downstream Products

• 181935-95-5 1-(3'-formylphenyl)-1-p-methoxybenzyloxy-ethane 
• 181935-98-8 1-{3-[1-(4-Methoxy-benzyloxy)-ethyl]-phenyl}-but-3-yn-1-ol 
• 181936-01-6 tert-Butyl-(1-{3-[1-(4-methoxy-benzyloxy)-ethyl]-phenyl}-but-3-ynyloxy)-dimethyl-silane 

Relevant academic research and scientific papers

Stereoselective synthesis of Macrolactin A analogues. Part 2: The C1-C14 fragment

A synthetic approach to the C1-C14 part of Macrolactin A analogues is presented. The sequence involving hydroboration-Pd° coupling reaction was found to be the most efficient in term of chemio- and stereo-selectivity to prepare the sensitive and functionalized E,Z diene unit.