161945-34-2

Upstream product

• 627064-10-2 1-methoxy-4-((undec-10-en-1-yloxy)methyl)benzene 
• 112-43-6 10-Undecen-1-ol 
• 824-94-2 p-methoxybenzyl chloride 

Downstream Products

• 161945-41-1 15-(4-Methoxy-benzyloxy)-2-(tetrahydro-pyran-2-yloxy)-pentadec-3-yn-6-ol 
• 161945-38-6 2-(tert-Butyl-dimethyl-silanyloxy)-15-(4-methoxy-benzyloxy)-pentadec-3-yn-6-ol 
• 161945-52-4 6-(tert-Butyl-diphenyl-silanyloxy)-15-(4-methoxy-benzyloxy)-pentadec-3-yn-2-ol 
• 161945-61-5 3-[2-(tert-Butyl-diphenyl-silanyloxy)-11-(4-methoxy-benzyloxy)-undecyl]-5-methyl-5H-furan-2-one 
• 161945-46-6 1-[14-(tert-Butyl-dimethyl-silanyloxy)-10-(tert-butyl-diphenyl-silanyloxy)-pentadec-12-ynyloxymethyl]-4-methoxy-benzene 

Relevant academic research and scientific papers

Conversion of Epoxides to 1,3-Dioxolanes Catalyzed by Tin(II) Chloride

Anhydrous tin(II) chloride is an efficient catalyst for the reaction of epoxides with acetone to prepare 2,2-dimethyl-1,3-dioxolanes (acetonides) in good to excellent yields. Mono-, di-, and trisubstituted epoxides participate equally well in this diastereospecific reaction. The use of single enantiomer epoxides under the reported conditions results in significant erosion of optical activity.