244612-56-4

Upstream product

• 244612-47-3 (4R,5R)-5-[(S)-2-(tert-Butyl-dimethyl-silanyloxy)-1-iodo-ethyl]-4-[(S)-2-(tert-butyl-dimethyl-silanyloxy)-1-trimethylsilanyloxy-ethyl]-dihydro-furan-2-one 
• 244612-45-1 6-(tert-butyl-dimethyl-silanyloxy)-3-[2-(tert-butyl-dimethyl-silanyloxy)-1-hydroxy-ethyl]-hex-4-enoic acid dimethylamide 
• 244612-44-0 (2S,5S)-2,5-dihydroxy-1,6-di(tert-butyldimethylsilyloxy)-3-hexene 
• 244612-53-1 (4S,5R)-4-((S)-1,2-Dihydroxy-ethyl)-5-((S)-2-hydroxy-1-iodo-ethyl)-dihydro-furan-2-one 
• 244612-54-2 (4R,5R)-4-[1,3]Dioxolan-2-yl-5-((S)-2-hydroxy-1-iodo-ethyl)-dihydro-furan-2-one 
• 6027-47-0 (2S,3E,5S)-1,2,5,6-tetrahydroxy-hex-3-ene 
• 3427-24-5 (2S,3E,5S)-1,2,5,6-tetrahydroxy-1,2:5,6-di-O-isopropylidene-hex-3-ene 
• 98-59-9 p-toluenesulfonyl chloride 
• 244612-55-3 (4R,5S)-4-[1,3]Dioxolan-2-yl-5-(2-hydroxy-ethyl)-dihydro-furan-2-one 

Relevant academic research and scientific papers

Enantiodivergent synthesis of both enantiomeric forms of substituted paraconic acids starting from N-mannitol as a chiral pool

Acetamide-acetal Claisen rearrangement of the C2-symmetric enediol easily derived from D-mannitol provided a chiral C8-building block, which was demonstrated to be versatile for divergent synthesis of both enantiomeric forms of substituted para