111099-55-9

Upstream product

• 111099-53-7 5,6α-cyclopropano-5α-cholestane-3β,7β-diol 7-benzoate 
• 111099-51-5 5,6α-cyclopropano-5α-cholestane-3β,7β-diol 3-acetate 
• 105220-79-9 3β-acetoxy-5α,6α-cyclopropa<5,6>cholestan-7α-ol 
• 111099-47-9 5,6α-cyclopropano-5α-cholestane-3β,7α-diol 7-benzoate 
• 111099-49-1 7α-benzoyloxy-5,6α-cyclopropano-5α-cholestan-3-one 
• 111099-52-6 5,6α-cyclopropano-5α-cholestane-3β,7β-diol 3-acetate 7-benzoate 
• 111099-46-8 5,6α-cyclopropano-5α-cholestane-3β,7α-diol 3-acetate 7-benzoate 

Downstream Products

• 111099-56-0 5,6α-cyclopropano-5α-cholestane-3α,7β-diol 7-benzoate 
• 111099-53-7 5,6α-cyclopropano-5α-cholestane-3β,7β-diol 7-benzoate 
• 111099-57-1 5,6α-cyclopropano-5α-cholestane-3α,7β-diol 3-acetate 7-benzoate 
• 111174-66-4 5,6α-cyclopropano-5α-cholestane-3α,7β-diol 3-methanesulfonate 7-benzoate 
• 111099-54-8 5,6α-cyclopropano-5α-cholestane-3β,7β-diol 3-methanesulfonate 7-benzoate 

Relevant academic research and scientific papers

SOLVOLYTIC REACTIONS OF EPIMERIC 3-METHANESULFONYLOXY-7-BENZOYLOXY-5α,6α-CYCLOPROPANOCHOLESTANES

Acetolysis of all possible configurational isomers of 3-methanesulfonyloxy-7-benzoyloxy-5α,6α-cyclopropanocholestanes is described and structure of the acetolysis products determined by spectroscopic methods.The 7-substituted derivatives show a greater propensity to elimination reactions than the 7-unsubstituted compounds.