287933-69-1

Upstream product

• 38238-75-4 (E)-2-chloroethenyl phenyl sulfone 
• 57044-25-4 (R)-oxiranemethanol 

Downstream Products

• 287933-70-4 (3S)-4-phenylsulfonyl-2,3-dihydrofuran-3-methanol 
• 287933-77-1 1-((1R,2R,3R)-tetrahydro-2-(1,1-dimethylethyldiphenyl)-silyloxy-3-(1,1-dimethylethyldiphenyl)-silyloxymethyl-1-furanyl)-4-(1,2,4-triazol-1-yl)-2(1H)-pyrimidinone 
• 448896-42-2 4-amino-1-((1R,2R,3R)-tetrahydro-2-(1,1-dimethylethyldiphenyl)-silyloxy-3-(1,1-dimethylethyldiphenyl)-silyloxymethyl-1-furanyl)-2(1H)-pyrimidinone 
• 448896-41-1 1-((1R,2R,3R)-tetrahydro-2-(1,1-dimethylethyldiphenyl)-silyloxy-3-(1,1-dimethylethyldiphenyl)-silyloxymethyl-1-furanyl)-2,4(1H,3H)-pyrimidinedione 
• 287933-80-6 6-N-benzoyl-9-((1R,2R,3S)-tetrahydro-2-acetoxy-3-(((4-methoxyphenyl)-diphenylmethoxy)-methyl)-1-furanyl)-9H-adenine 
• 287933-94-2 5-methyl-1-((1R,2R,3S)-tetrahydro-2-hydroxy-3-(((4-methoxyphenyl)-diphenylmethoxy)-methyl)-1-furanyl)-2,4(1H,3H)-pyrimidinedione 
• 287933-84-0 5-methyl-1-((1R,2S,3S)-tetrahydro-2-hydroxy-3-(((4-methoxyphenyl)-diphenylmethoxy)-methyl)-1-furanyl)-2,4(1H,3H)-pyrimidinedione 
• 287933-83-9 5-methyl-1-((1R,2R,3R)-tetrahydro-2-azido-3-(1,1-dimethylethyldiphenyl)-silyloxymethyl-1-furanyl)-2,4(1H,3H)-pyrimidinedione 
• 287933-97-5 2,2'-anhydro-5-methyl-1-((1R,2S,3S)-tetrahydro-2-hydroxy-3-(((4-methoxyphenyl)-diphenylmethoxy)-methyl)-1-furanyl)-2,4(1H,3H)-pyrimidinedione 
• 287933-75-9 5-methyl-1-((1R,2R,3R)-tetrahydro-2-hydroxy-3-(1,1-dimethylethyldiphenyl)-silyloxymethyl-1-furanyl)-2,4(1H,3H)-pyrimidinedione 
• 287933-76-0 1-((1R,2R,3R)-tetrahydro-2-hydroxy-3-(1,1-dimethylethyldiphenyl)-silyloxymethyl-1-furanyl)-2,4(1H,3H)-pyrimidinedione 
• 287933-82-8 2,2'-anhydro-5-methyl-1-((1R,2S,3R)-tetrahydro-2-hydroxy-3-(1,1-dimethylethyldiphenyl)-silyloxymethyl-1-furanyl)-2,4(1H,3H)-pyrimidinedione 
• 287933-90-8 (3R)-3-(((4-methoxyphenyl)-diphenylmethoxy)-methyl)-4-phenylsulfonyl-2,3-dihydrofuran 
• 287933-71-5 (3R)-3-((((1,1-dimethylethyl)-diphenyl)-silyloxy)methyl)-4-phenylsulfonyl-2,3-dihydrofuran 

Relevant academic research and scientific papers

Efficient synthesis of several methylene-expanded oxetanocin nucleoside analogues

S-Glycidol 4 has been converted by a direct route via the dihydrofuran- 3-methanols 9ab into a series of methylene-expanded oxetanocin nucleoside analogues, e.g., analogues of the normal nucleosides 2 and the known antiviral nucleosides, AZT, FdT, and ddC, 3. (C) 2000 Elsevier Science Ltd.