180164-97-0

Upstream product

• 130669-74-8 (1S,2S,5R,6R)-3-bromo-5,6-epoxy-1,2-O-isopropylidencyclohex-3-en-1,2-diol 
• 100-51-6 benzyl alcohol 
• 130669-75-9 (3aS,7aS)-4-bromo-2,2-dimethyl-3a,7a-dihydro-1,3-benzodioxole 
• 67451-62-1 cis-(1S,2S)-1,2-dihydroxy-3-bromocyclohexa-3,5-diene 

Downstream Products

• 213017-72-2 (3aS,4R,5S,7aR)-5-Benzyloxy-2,2-dimethyl-3a,4,5,7a-tetrahydro-benzo[1,3]dioxol-4-ol 
• 180165-00-8 C₃₄H₄₄O₁₀ 
• 180165-05-3 C₄₃H₅₂Br₄O₁₃ 
• 180165-07-5 C₄₃H₆₄O₂₁ 
• 180165-06-4 C₄₃H₅₆O₁₃ 
• 180164-99-2 C₃₄H₄₁Br₃O₁₀ 
• 180165-01-9 C₃₄H₅₀O₁₆ 
• 213019-09-1 (1R,2R,3S,4R,5S,6R)-6-Benzyloxy-cyclohexane-1,2,3,4,5-pentaol 
• 681816-05-7 (3aR,4S,5S,6S,7R,7aS)-6-((3aS,4R,5S,6S,7S,7aR)-5-Benzyloxy-6,7-dihydroxy-2,2-dimethyl-hexahydro-benzo[1,3]dioxol-4-yloxy)-2,2-dimethyl-hexahydro-benzo[1,3]dioxole-4,5,7-triol 
• 682790-48-3 (2R,3R,3aS,6aR)-2-((2S,3R,3aS,6aR)-2-Benzyloxy-5,5-dimethyl-hexahydro-1,4,6-trioxa-cyclopropa[e]inden-3-yloxy)-5,5-dimethyl-hexahydro-1,4,6-trioxa-cyclopropa[e]inden-3-ol 
• 681816-04-6 (3aS,4R,5S,7aR)-5-((3aR,4R,5S,7aR)-5-Benzyloxy-2,2-dimethyl-3a,4,5,7a-tetrahydro-benzo[1,3]dioxol-4-yloxy)-2,2-dimethyl-3a,4,5,7a-tetrahydro-benzo[1,3]dioxol-4-ol 
• 180164-98-1 (3aS,4R,5S,7aS)-5-((3aS,4R,5S,7aS)-5-Benzyloxy-7-bromo-2,2-dimethyl-3a,4,5,7a-tetrahydro-benzo[1,3]dioxol-4-yloxy)-7-bromo-2,2-dimethyl-3a,4,5,7a-tetrahydro-benzo[1,3]dioxol-4-ol 

Relevant academic research and scientific papers

New oligomers of conduritol-F and muco-inositol. Synthesis and biological evaluation as glycosidase inhibitors

Several oligomers possessing the configuration of conduritol-F and muco-inositol have been prepared and tested against six glycosidase enzymes. Electrochemical dehalogenation and reductive deprotection of cinnamyl ethers are featured in the reported syntheses. The synthesis, properties, and biological activities are investigated.

Inositol synthesis: Concise preparation of L-chiro-inositol and muco- inositol from a common intermediate

Fully stereoselective large-scale syntheses have been attained for L- chiro-inositol (2) and muco-inositol (3) by means of controlled peripheral oxygenation of cyclohexadiene diol 1.

Toluene-dioxygenase-mediated cis-dihydroxylation of aromatics in enantioselective synthesis. Iterative glycoconjugate coupling strategy and combinatorial design for the synthesis of oligomers of nor-saccharides, inositols and pseudosugars with interesting

Vinyl epoxides 18 and 31 and vinylaziridines 24 and 25 derived from chloro- or bromocyclohexadiene-cis-diols 9 have been condensed with protected cyclitols 19, 37, and 46 in an iterative manner to generate dimeric, trimeric and tetrameric conduritol or am

Concise syntheses of 1,2-L-chiro-inositol conjugates and oligomers - A novel class of saccharide mimics with promising molecular properties

Calcium complexes with novel amino-inositol conjugates to form secondary extended helical structures are reported.