151477-85-9

Upstream product

• 36199-02-7 3,4-di-O-benzyl-D-mannitol 
• 1707-77-3 1,2:5,6-di-O-isopropylidene-D-mannitol 
• 111476-62-1 3,4-di-O-benzyl-1,2:5,6-di-O-isopropylidene-D-mannitol 
• 722539-36-8 3,4-di-O-benzyl-1,2:5,6-di-O-sulfinyl-D-mannitol 

Downstream Products

• 111555-72-7 R,R-3,4-dibenzyloxy-threo-hexa-1,5-diene 
• 171667-67-7 (3S,4R,5R,6S)-4,5-Bis-benzyloxy-thiepane-3,6-diol 
• 200191-55-5 (3S,4R,5S,6S)-4,5-Bis-benzyloxy-6-hydroxymethyl-tetrahydro-thiopyran-3-ol 
• 138328-94-6 ((1S,2R,3R,4S)-4-tert-Butoxycarbonylamino-2,3-dihydroxy-1-phenethyl-6-phenyl-hexyl)-carbamic acid tert-butyl ester 
• 502699-56-1 (2S,2'S)-<(1R,2R)-1,2-dibenzyloxy-ethan-diyl>bis-aziridine 
• 151477-86-0 1,6-diazido-1,6-dideoxy-3,4-di-O-benzyl-D-mannitol 
• 156856-23-4 (2S,2'S)-<(1R,2R)-1,2-dibenzyloxy-ethan-diyl>bis(1-tert-butoxycarbonyl)-aziridine 
• 151477-88-2 ((1S,2R,3R,4S)-2,3-Bis-benzyloxy-4-tert-butoxycarbonylamino-1-phenethyl-6-phenyl-hexyl)-carbamic acid tert-butyl ester 

Relevant academic research and scientific papers

Heterocyclisation of free or partially protected alditols via their bis- cyclic sulfate derivatives. Versatile synthesis of aza and thiodeoxyanhydroalditol with erythro, threo, arabino, gulo, talo or manno configuration

The his-cyclic sulfate derivatives of erythritol (1), D,L-threito1 (5), 3,4-di-O-benzyl-D-mannitol (9), 1,2-O-isopropylidene-D-mannitol (14) and l-O- benzyl-D,L-xylito1 (18) were submitted to nucleophilic attack by allylamine or sodium sulfide. In both ca

Applications of Cyclic Sulfates of vic-Diols: Synthesis of Episulfides, Olefins, and Thio Sugars

A new efficient and expeditious one-pot synthesis of thiiranes and olefins from cyclic sulfates of inc-diols is described. Opening of cyclic sulfates with potassium thioacetate or potassium thiocyanate followed by treatment with sodium methoxide led to ep

STEREOSELECTIVE SYNTHESIS OF DIAMINO DIOL DERIVATIVES WITH C2-AXIS OF SYMMETRY

An efficient and streocontrolled synthesis of C2-symmetric diamino diol derivatives (7) was achieved through selective opening of N-Boc bis-aziridine (6), prepared from D-mannitol via cyclic sulfate (4).