133443-76-2

Upstream product

• 111248-46-5 (2R,4aS,5aS,8R,9aR,9bR)-2,8-Diphenyl-hexahydro-bis[1,3]dioxino[5,4-b;4',5'-d]pyrrol-5-ylamine 
• 111248-46-5 N-amino-1,3:4,6-di-O-benzylidene-2,5-dideoxy-2,5-imino-L-iditol 
• 28224-73-9 1,3:4,6-di-O-benzylidene-D-mannitol 
• 111275-74-2 1,3:4,6-di-O-benzyliidene-2,5-di-O-trifluoromethylsulphonyl-D-mannitol 
• 111275-74-2 Trifluoro-methanesulfonic acid (2R,4S,5R,2'R,4'S,5'R)-2,2'-diphenyl-5'-trifluoromethanesulfonyloxy-[4,4']bi[[1,3]dioxanyl]-5-yl ester 
• 28224-74-0 1,3:4,6-di-O-benzylidene-2,5-di-O-methanesulfonyl-D-mannitol 
• 144266-28-4 2,5-dideoxy-2,5-N-benzylimino-1,3:4,6-di-O-benzylidene-L-iditol 

Downstream Products

• 158867-55-1 (2R,4aS,5aS,8R,9aR,9bR)-1-perhydro-2,8-diphenyl-2H,5H,8H-bis<1,3>dioxino<5,4-b:4',5'-d>pyrrolidine 
• 168753-02-4 N,N'-(diselenodi-2,1-phenylenemethylene)bis[1,3:4,6-di-O-benzylidene-2,5-dihydro-2,5-epimino-L-iditol] 
• 105015-44-9 (2S,3R,4R,5S)-3,4-dihydroxy-2,5-bis(hydroxymethyl)pyrrolidine 
• 1072809-76-7 C₂₉H₃₇NO₅ 
• 1072809-73-4 C₂₉H₃₃NO₅ 
• 1072809-45-0 C₂₉H₃₃NO₅ 
• 133378-87-7 1,3:4,6-Di-O-benzylidene-2,5-dideoxy-2,5-<<(1S,4R)-2-oxa-3-azabicyclo<2.2.2>oct-5-ene-3-carbonyl>imino>-L-iditol 
• 144266-33-1 2-((2R,4aS,5aS,8R,9aR,9bR)-2,8-Diphenyl-hexahydro-bis[1,3]dioxino[5,4-b;4',5'-d]pyrrol-5-yl)-1,1-diphenyl-ethanol 
• 144266-42-2 2-((2R,4aS,5aS,8R,9aR,9bR)-2,8-Diphenyl-hexahydro-bis[1,3]dioxino[5,4-b;4',5'-d]pyrrol-5-yl)-ethanol 

Relevant academic research and scientific papers

Synthesis of new analogues of salacinol containing a pendant hydroxymethyl group as potential glycosidase inhibitors

The synthesis of new analogues of the naturally occurring glycosidase inhibitor, salacinol, and its ammonium analogue, ghavamiol is described. These analogues contain an additional hydroxymethyl group at C-1, which was intended to form additional polar co

Short-step synthesis of chiral C2-symmetric 2,3,4,5-tetrasubstituted pyrrolidines from D-mannitol and their use as chiral ligands in the reaction of diethylzinc and benzaldehyde

(3R,4R)-bis(hydroxy)-(2S,5S)-bis(hydroxymethyl)-pyrrolidine and related chiral C2-symmetric pyrrolidines including D2-symmetric 1,2-bis(1-pyrrolidino)-ethanes and N-hydroxyethylpyrrolidines were synthesized highly practically from D-

Asymmetric Diels-Alder Cycloadditions with C2-Symmetrical Chiral Carbamoylnitroso Dienophiles

The C2-symmetrical chiral pyrrolidines 2 and 3 are of opposite helicity.The corresponding N-acylnitroso dienophiles 6 and 7 react in good yield with cyclohexadiene, leading thereby with excellent diastereoisomeric excess to the expected Diels-A

SYNTHESIS OF (2S,5S)-BISHYDROXYMETHYL-(3R,4R)-BISHYDROXYPYRROLIDINE FROM D-MANNITOL

A short, efficient, and practical synthesis of (2S,5S)-bishydroxymethyl-(3R,4R)-bishydroxypyrrolidine from D-mannitol involving five sequential reactions (benzylidenation, trifluoromethanesulphonation, hydrazinolysis, hydrogenolysis, and deacetalisation)

A Short and Practical Synthesis of (2S,5S)-Bishydroxymethyl-(3R,4R)-bishydroxypyrrolidine

D-Mannitol has been converted by five sequential reactions (benzylidenation, trifluoromethanesulphonation, hydrazinolysis, hydrogenolysis, and deacetalisation) into (2S,5S)-bishydroxymethyl-(3R,Ρ)-bishydroxypyrrolidine.