150638-41-8

Upstream product

• 77312-71-1 diethyl (2R,3R)-2,3-bis(benzyloxy)butane-1,4-dioate 
• 113427-43-3 1,4-di-O-benzyl-L-threitol 
• 868672-20-2 (2S,3S)-2,3-bis(phenylmethyloxy)-1,4-bis(methylsulfonyloxy)butane 
• 113303-29-0 (2S,3S)-(+)-2,3-bis(phenylmethoxy)-1,4-bis<<(4-methylphenyl)sulfonyl>oxy>butane 

Downstream Products

• 329363-65-7 (2S,3S,4S)-1-hydroxy-2-ethenyl-3,4-bis(benzyloxy)pyrrolidine 
• 1352617-03-8 (3S,4S)-3,4-bis(benzyloxy)-6-[(3aS,4S,6R,6aS)-tetrahydro-4-methoxy-2,2-dimethylfuro[3,4-d][1,3]dioxol-6-yl]-1-azabicyclo-[3.2.0]heptan-7-one 
• 1352617-01-6 (3S,4S)-3,4-bis(benzyloxy)-6-[(3aR,6R,6aS)-tetrahydro-2,2-dimethylfuro[3,4-d][1,3]dioxol-6-yl]-1-azabicyclo[3.2.0]heptan-7-one 
• 1352616-99-9 (3S,4S)-3,4-bis(benzyloxy)-6-[(3aR,5R,6S,6aR)-6-(benzyloxy)-tetrahydro-2,2-dimethylfuro[2,3-d][1,3]dioxol-5-yl]-1-azabicyclo-[3.2.0]heptan-7-one 
• 1352617-07-2 1,4-bis[(3aR,4R,6R,6aR)-tetrahydro-6-methoxy-2,2-dimethylfuro[3,4-d][1,3]dioxol-4-yl]buta-1,3-diyne 
• 1352617-05-0 1,4-bis[(3aR,5R,5aS,8aS,8bR)-tetrahydro-2,2,7,7-tetramethyl-3aH-bis[1,3]dioxolo[4,5-b:4',5'-d]pyran-5-yl]buta-1,3-diyne 
• 1352617-00-5 (3S,4S)-3,4-bis(benzyloxy)-6-[(3aR,5R,5aS,8aS,8bR)-tetrahydro-2,2,7,7-tetramethyl-3aH-bis[1,3]dioxolo[4,5-b:4',5'-d]pyran-5-yl]-1-azabicyclo[3.2.0]heptan-7-one 

Relevant academic research and scientific papers

C4 branched polyhydroxy pyrrolidine compound and preparation method and application thereof

The invention relates to the field of glycosidase inhibitors, in particular to a C4 branched polyhydroxy pyrrolidine compound and a preparation method and application thereof. The structure of the C4 branched polyhydroxy pyrrolidine compound is as is shown in the description. The C4 branched polyhydroxy pyrrolidine compound is good in glycosidase inhibition activity and has potential medicinal value.

Samarium diiodide-mediated reductive couplings of chiral nitrones with aldehydes/ketones and acyl chlorides

The SmI2-mediated and H2O-promoted reductive cross-coupling reactions of the l-tartaric acid derived nitrone (3S,4S)-8 with aldehydes/ketones, and the l-malic acid derived nitrone (S)-6 with aliphatic acyl chlorides have been investi

Manganese dioxide oxidation of hydroxylamines to nitrones

Several structurally differentiated N,N-dialkylhydroxylamines were oxidised to the corresponding nitrones using MnO2. Manganese dioxide revealed an efficient and mild reagent for oxidation of hydroxylamines, showing a level of regioselectivity