74642-66-3

Upstream product

• 98-88-4 benzoyl chloride 
• 98-59-9 p-toluenesulfonyl chloride 
• 74628-97-0 bis-((S)-β-benzoyloxy-β'-hydroxy-isopropoxy)-methane 
• 74628-88-9 C₃₅H₃₆O₁₂S₂ 
• 96662-57-6 (2S)-2,3-dihydroxypropyl benzoate 
• 74628-94-7 O¹,O⁶-dibenzoyl-O²,O⁵-methanediyl-D-mannitol 
• 29751-66-4 1-Benzoyloxy-3-hydroxy-2-propanone 

Downstream Products

• 74629-13-3 1,2-di-O-benzoyl-3-O-tosyl-sn-glycerol 
• 13495-39-1 1-benzoyloxy-2,3-bis-(4-nitro-benzoyloxy)-propane 
• 14892-44-5 1,3-bis-benzoyloxy-2-(4-nitro-benzoyloxy)-propane 
• 16548-87-1 1,2-bis-benzoyloxy-3-(4-nitro-benzoyloxy)-propane 
• 99336-06-8 di-O-benzoyl-1,2 iododesoxy-3 ns-glycerol 
• 99336-07-9 O-benzoyl-1 O-p-methoxybenzoyl-2 iododesoxy-3 ns-glycerol 
• 99336-08-0 O-benzoyl-1 O-p-nitrobenzoyl-2 iododesoxy-3 ns-glycerol 
• 13529-48-1 C₂₆H₂₄O₈ 
• 74629-10-0 C₂₅H₂₁NO₉ 
• 74629-10-0 1-O-benzoyl-2-O-p-nitrobenzoyl-3-O-p-methoxybenzoyl-sn-glycerol 
• 121787-43-7 (2S)-oxiran-2-ylmethyl benzoate 
• 99336-05-7 O-benzoyl-1 iododesoxy-3 ns-glycerol 

Relevant academic research and scientific papers

Enatioselective Microbial Reduction of Monoesters of 1,3-Dihydroxypropanone: Synthesis of (S)- and (R)-1,2-O-Isopropylideneglycerol

The reduction of 3-benzoyloxy-1-hydroxypropanone with bakers' yeast proceeds enantioselectively to afford (S)-3-benzoyloxy-1,2-propanediol, which may be further converted into (S)-(benzoyloxymethyl)oxirane.The bioreduction with fermenting yeast of 1-acetoxy-3-benzyloxypropanones gives (R)-1-benzyloxy-3-acetoxy-2-propanol which can be used for the preparation of both (S)- and (R)-1,2-O-isopropylideneglycerol.

A Possible Model for a New Chiral Glyceride Synthesis. Part 2. Synthesis of 1,3-Di-O-aroyl- and 1-O-Aroyl-3-O-tosyl-sn-glycerols from 2,5-O-Methylene-D-mannitol

1,3-Di-O-aroyl- and 1-O-aroyl-3-O-tosyl-sn-glycerols have been prepared from D-mannitol via 2,5-O-methylene-D-mannitol.Some 1,3-diglycerides have also been synthesised from 3-O-aroyl-sn-glycerols.The optical rotations and the structure of the 1,3-diglycer