286474-94-0

Upstream product

• 135943-81-6 (+)-(4S,6R)-8-phenyloct-1-ene-4,6-diol 
• 77-76-9 2,2-dimethoxy-propane 
• 133271-03-1 (R)-3-Hydroxy-5-phenyl-pentanal 
• 60340-28-5 (R)-1-phenyl-hex-5-en-3-ol 
• 104-53-0 3-phenyl-propionaldehyde 

Downstream Products

• 86117-01-3 (4R,6R)-(+)-4-hydroxy-6-(2-phenylethyl)-tetrahydro-2H-pyran-2-one 

Relevant academic research and scientific papers

Empirical model for the molar rotations of syn-2,2-dimethyl-1,3-dioxanes.

[structure: see text] A useful method for the prediction of molar rotation ([Phi]) of syn-2,2-dimethyl-1,3-dioxanes (acetonides) is described. A series of acetonides were prepared by standard methods. A simple additive relationship between the substituent

Enantioselective allyltitanation. Application to the synthesis of lactone units related to compactin and mevinolin

The enantioselective convergent synthesis of two different models of the lactone units of compactin and mevinolin was achieved using two consecutive enantioselective allyltitanations of aldehydes.