259674-79-8

Upstream product

• 1053243-67-6 (2S,3R,4S)-2,3-Bis-(tert-butyl-dimethyl-silanyloxy)-4-hydroxy-oct-7-enoic acid benzylamide 
• 259674-78-7 (2S,3R,4R,5S)-2-But-3-enyl-3,4-bis-(tert-butyl-dimethyl-silanyloxy)-5-phenyl-tetrahydro-furan 
• 259674-77-6 (3S,4R,5S)-5-But-3-enyl-3,4-bis-(tert-butyl-dimethyl-silanyloxy)-dihydro-furan-2-one 

Downstream Products

• 259674-80-1 3-[(2S,3R,4R,5S)-3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-5-phenyl-tetrahydro-furan-2-yl]-propionic acid methyl ester 

Relevant academic research and scientific papers

Asymmetric synthesis of tetrasubstituted tetrahydrofuran, 2- epigoniothalesdiol, employing stereoselective hydrogenation

An efficient and stereodefined process is described for the preparation of a 3,4-dihydroxy-2,5-disubstituted tetrahydrofuran ring with the contiguous stereogenic centers and the asymmetric synthesis of 2-epigoniothalesdiol is also reported by featuring the elaboration of the functionalized homochiral lactone derived from C2-imide.