796843-99-7

Upstream product

• 2211-94-1 4-methoxybenzyloxy ester of (S)-glycidol 
• 1730-25-2 allylmagnesium bromide 
• 150-76-5 4-methoxy-phenol 

Downstream Products

• 316808-27-2 1-Methoxy-4-((R)-2-methoxymethoxy-hex-5-enyloxy)-benzene 
• 316808-34-1 2,2-Dimethyl-propionic acid (3S,5R,8R)-3,5,8-tris-methoxymethoxy-9-(4-methoxy-phenoxy)-nonyl ester 
• 316808-32-9 1-Methoxy-4-((2R,5R,7S)-2,5,7-tris-methoxymethoxy-dec-9-enyloxy)-benzene 
• 316808-30-7 (4S,6R,9R)-9-Methoxymethoxy-10-(4-methoxy-phenoxy)-dec-1-ene-4,6-diol 
• 316808-29-4 (4R,7R)-7-Methoxymethoxy-8-(4-methoxy-phenoxy)-oct-1-en-4-ol 
• 316808-28-3 (R)-4-Methoxymethoxy-5-(4-methoxy-phenoxy)-pentanal 

Relevant academic research and scientific papers

Enantioselective allyltitanation. Efficient synthesis of the C1-C14 polyol subunit of amphotericin B

(Matrix presented) An efficient synthesis of the C1-C14 fragment of amphotericin B is described. This synthesis is based on the formation of syn-1,3-diols from enantioselective allyltitanation of unprotected β-hydroxyaldehydes.