129634-46-4

Upstream product

• 18162-48-6 tert-butyldimethylsilyl chloride 
• 129634-43-1 4-<(tert-Butyl)dimethylsilyloxy>-3-(<(tert-butyl)dimethylsilyloxy>methyl)-2-ethyl-2,3-dihydroxybutanenitrile 
• 129634-44-2 1-<(tert-Butyl)dimethylsilyloxy>-2-(<(tert-butyl)dimethylsilyloxy>methyl)-2-hydroxypentan-3-one 
• 127382-65-4 1,3-bis-O-(tert-butyldimethylsilyl)-1,3-dihydroxy-2-propanone 
• 129634-45-3 1-<(tert-Butyl)dimethylsilyloxy>-2-(<(tert-butyl)dimethylsilyloxy>methyl)-2-(trimethylsilyloxy)pentan-3-one 
• 98-88-4 benzoyl chloride 
• 129634-42-0 4-<(tert-Butyl)dimethylsilyloxy>-3-(<(tert-butyl)dimethylsilyloxy>methyl)-2-ethyl-3-hydroxy-2-<(tetrahydro-2H-pyran-2-yl)oxy>butanenitrile 

Downstream Products

• 129634-48-6 2,2-Bis(<(tert-butyl)dimethylsilyloxy>methyl)-4-methyl-5-phenylfuran-3(2H)-one 
• 129634-47-5 2,2-Bis(hydroxymethyl)-4-methyl-5-phenylfuran-3(2H)-one 

Relevant academic research and scientific papers

53. Synthetic Studies Directed toward the Pseurotins. Part II. Synthesis of Related Highly Functionalized Furan-3(2H)-ones

The synthesis of 2,2-bis(hydroxymethyl)-4-methyl-5-phenylfuran-3(2H)-one (9), 5--2,2-bis(hydroxymethyl)-4-methylfuran-3(2H)-one (24), and 5--2-(hydroxymethyl)-4-methylfuran-3(2H)-one (28), which represent more advanced, suitably functionalized intermediates for the synthesis of pseurotin A (1), a secondary metabolite of Pseudeurotium ovalis Stolk, is described.