137765-97-0

Upstream product

• 137676-01-8 (2S,4R)-4-((1S,2S,5R)-1-Allyl-2-isopropyl-5-methyl-cyclohexyloxy)-pentan-2-ol 
• 2747-38-8 methyltrichlorotitanium 
• 99032-03-8 (3S)-3-(Benzyloxy)butanal 
• 97536-46-4 (2R,4S,6S,7S,10R)-7-Isopropyl-2,4,10-trimethyl-1,5-dioxa-spiro[5.5]undecane 
• 100-39-0 benzyl bromide 

Relevant academic research and scientific papers

Enantioselective ring cleavage of dioxane acetals mediated by a chiral Lewis acid: Application to asymmetric desymmetrization of meso-1,3-diols

Equation presented Phenylalanine-derived B-aryl-N-tosyloxazaborolidinones selectively activate one of two enantiotopic oxygen atoms in prochiral anti dioxane acetals derived from meso-1,3-diols, leading to enantioselective formation of ring-cleavage produ

Enantiodifferentiating Functionalization of Prochiral Diols by Highly Stereoselective Ring-Cleavage Reaction of Spiroacetals Derived from l-Menthone with Allyltrimethylsilane-Titanium-Tetrachloride

Enantiodifferentiating transformation of prochiral diols possessing ?-symmetry was realized by the utilization of titanium tetrachloride-promoted selective ring-cleavage reaction of spiroacetals derived from the diols and l-menthone with allyltrimethylsil