114935-25-0

Upstream product

• 100-39-0 benzyl bromide 
• 482621-00-1 (R)-1-(4-Methoxy-benzyloxy)-3-trityloxy-propan-2-ol 
• 824-94-2 p-methoxybenzyl chloride 
• 109786-77-8 (S)-3-((4-methoxybenzyl)oxy)propane-1,2-diol 
• 637774-36-8 (R)-1-t-butyldimethylsilyloxy-3-(p-methoxyphenyl)methoxyl-2-propanol 
• 123-11-5 4-methoxy-benzaldehyde 
• 114935-17-0 1,3(R):4,6(R)-Bis-O-(4-methoxy-benzylidene)-D-mannitol 
• 114935-21-6 2,5-di-O-benzyl-1,6-bis-O-(4-methoxy-benzyl)-D-mannitol 
• 114935-18-1 2,5-di-O-benzyl-1,3(R):4,6(R)-bis-O-(4-methoxy-benzylidene)-D-mannitol 

Downstream Products

• 114935-23-8 (R)-2-benzyloxy-3-(4-methoxy-benzyloxy)-1-(2,2-dimethyl-propionyloxy)-propane 

Relevant academic research and scientific papers

Stereoselective total synthesis of sporiolide B and attempted synthesis of sporiolide A

A simple and efficient stereoselective total synthesis of sporiolide B and attempted synthesis of sporiolide A, from epichlorohydrin, using asymmetric synthetic approach is reported. The key reactions involved are Sharpless epoxidation, Jacobsen reaction, syn-allylation, Yamaguchi esterification, and Grubbs ring-closing metatheses reaction to result in the macrocyclic ring system.

Stereoselective synthesis of the head group of archaeal phospholipid PGP-Me to investigate bacteriorhodopsin-lipid interactions

Phosphatidylglycerophosphate methyl ester (PGP-Me), a major constituent of the archaeal purple membrane, is essential for the proper proton-pump activity of bacteriorhodopsin (bR). We carried out the first synthesis of the bisphosphate head group of PGP-M