62102-44-7

Upstream product

• 62102-45-8 2,3,4,5-tetra-O-benzyl-L-iditol 
• 24558-77-8 3,4,5,6-tetra-O-benzyl inositol 
• 488-45-9 L-iditol 
• 100-39-0 benzyl bromide 
• 110522-67-3 C₇₂H₆₆O₆ 
• 159346-83-5 1,6-di-O-triphenylmethyl-L-iditol 
• 487-44-5 D-(+)-glucuronic acid γ-lactone 
• 100-44-7 benzyl chloride 
• 114343-02-1 (2S,3S,3aR,5S,6R,6aR)-2,5-Dimethoxy-hexahydro-furo[3,2-b]furan-3,6-diol 
• 114343-01-0 (3aR,3bS,5S,6S,6aR,7aR)-5-Methoxy-2,2-dimethyl-hexahydro-furo[2',3':4,5]furo[2,3-d][1,3]dioxol-6-ol 
• 94926-00-8 2,5-di-O-benzyl-L-iditol 
• 110522-64-0 (2S,3S,3aS,5S,6R,6aS)-3,6-Bis-benzyloxy-2,5-dimethoxy-hexahydro-furo[3,2-b]furan 
• 195873-74-6 C₃₆H₃₈O₄ 
• 110522-66-2 (2S,3S,4S,5S)-2,5-Bis-benzyloxy-1,6-bis-trityloxy-hexane-3,4-diol 

Downstream Products

• 676259-90-8 (3S,4R,5R,6S)-1-Benzyl-3,4,5,6-tetrakis-benzyloxy-azepane 
• 24558-77-8 3,4,5,6-tetra-O-benzyl inositol 
• 110550-26-0 (1R,2R,3S,4R,5R,6S)-3,4,5,6-tetrakis(benzyloxy)cyclohexane-1,2-diol 
• 110550-24-8 1D-2,3,4,5-tetra-O-benzyl-chiro-inositol 

Relevant academic research and scientific papers

N-heterocyclic carbene-catalyzed benzoin strategy for divergent synthesis of cyclitol derivatives from alditols

A divergent synthesis of cyclitol derivatives has been developed utilizing an N-heterocyclic carbene-catalyzed benzoin-type cyclization of C2-symmetrical dialdoses. The resulting inososes are versatile intermediates, which are readily converted

Synthesis of differentially protected myo- and chiro-inositols from D-xylose: Stereoselectivity in intramolecular SmI2-promoted pinacol reactions

Methods for the enantioselective conversion of D-xylose into differentially protected myo-inositol and L-chiro-inositol have been developed. The key transformation is a highly diastereoselective intramolecular SmI 2-promoted pinacol coupling. T

Syntheses of tetrahydroxyazepanes from chiro-inositols and their evaluation as glycosidase inhibitors

Two pairs of C2-symmetric tetrahydroxyazepanes [(-), (+)-1 and (-), (+)-2] have been synthesized from the enantiomeric chiro-inositols and evaluated as glycosidase inhibitors. Alternative syntheses of ido-tetrahydroxyazepanes (-)- and (+)-2 fro

Samarium diiodide-mediated synthesis of D-3,4,5,6-tetra-O-benzyl-myo-inositol

The preparation of D-3,4,5,6-tetra-O-benzyl-myo-inositol in 5 steps from L-iditol is described, the cyclization step being a dialdehyde reductive coupling mediated by SmI2.

Synthesis of Optically Active Inositol Derivatives Starting from D-Glucurono-6,3-lactone

D-Glucurono-6,3-lactone was converted to optically active and partially protected inositols.The synthetic strategy involves an efficient conversion of the D-gluco configuration to the L-ido configuration and dials to cyclitols.