124561-23-5

Upstream product

• 141171-64-4 (3aR,5R,7R,7aS)-5,7-Dihydroxy-2-phenyl-hexahydro-benzo[1,3]dioxole-5-carboxylic acid 
• 141171-56-4 (3aS,4R,7aR)-6-Methylene-2-phenyl-hexahydro-benzo[1,3]dioxol-4-ol 
• 32384-44-4 (1S,3R,4R,5R)-4,5-Benzylidenedioxy-1-hydroxycyclohexane-1,3-carbolactone 
• 100-52-7 benzaldehyde 
• 77-95-2 D-(-)-quinic acid 
• 124561-23-5 <2S-(2α,3aα,5β,7α,7aα)>-hexahydro-5-(hydroxymethyl)-2-phenyl-1,3-benzodioxole-5,7-diol 
• 216662-57-6 (1S,3R,4R,5R)-3,4-O-Benzylidene-1,3,4-trihydroxy-6-oxabicyclo<3.2.1>octan-7-one 

Downstream Products

• 134932-01-7 <1R-(1α,3α,4β,5α)>-1,3,4-trihydroxy-5-(phosphonomethyl)cyclohexane-1-carboxylic acid 
• 141171-61-1 <5R-(5α,7α,8β,9β)>-7-(benzyloxy)-8,9-epoxy-2,2-dimethyl-1,3-dioxaspiro<4.5>decane 
• 141171-60-0 <5R-(5α,7α,8β,9β)>-7-(benzoyloxy)-8-bromo-2,2-dimethyl-1,3-dioxaspiro<4.5>decan-9-ol 
• 141197-74-2 <1R-(1α,3α,4β,5α)>-1-(hydroxymethyl)-5-<(diisopropoxyphosphinyl)methyl>cyclohexan-1,3,4-triol 
• 141171-63-3 <1R-(1α,3α,4β,5α)>-1,3,4-trihydroxy-5-<(diisopropoxyphosphinyl)methyl>cyclohexan-1-carboxylic acid 
• 141171-62-2 ((1S,2R,3R,5R)-3-Benzyloxy-2,5-dihydroxy-5-hydroxymethyl-cyclohexylmethyl)-phosphonic acid diisopropyl ester 
• 141171-65-5 (3aR,5S,7R,7aS)-5-Benzoyloxy-7-hydroxy-2-phenyl-hexahydro-benzo[1,3]dioxole-5-carboxylic acid 
• 141171-58-6 (3aR,5S,7R,7aS)-5-Benzoyloxy-7-hydroxy-2-phenyl-hexahydro-benzo[1,3]dioxole-5-carboxylic acid methyl ester 
• 141171-59-7 C₂₂H₂₁BrO₇ 
• 141269-65-0 <5R-(5α,7α,8β,9α)>-7-(benzyloxy)-2,2-dimethyl-9-<(diisopropoxyphosphinyl)methyl>-1,3-dioxaspiro<4.5>decan-8-ol 
• 124561-23-5 (3aS,4R,6S,7aR)-6-Hydroxymethyl-2-phenyl-hexahydro-benzo[1,3]dioxole-4,6-diol 
• 141171-64-4 (3aR,5S,7R,7aS)-5,7-Dihydroxy-2-phenyl-hexahydro-benzo[1,3]dioxole-5-carboxylic acid 
• 135525-92-7 ((5S,7S,8R,9R)-9-Benzyloxy-8-hydroxy-2,2-dimethyl-1,3-dioxa-spiro[4.5]dec-7-ylmethyl)-phosphonic acid diisopropyl ester 
• 135525-93-8 ((1S,3R,5S)-3-Benzyloxy-5-hydroxy-5-hydroxymethyl-2-oxo-cyclohexylmethyl)-phosphonic acid diisopropyl ester 

Relevant academic research and scientific papers

13C and 1H NMR Investigations of Quinic Acid Derivatives: Complete Spectral Assignment and Elucidation of Preferred Conformations

The 1H and 13C NMR spectra of 23 quinic acid derivatives are reported.The complete assignment of the 1H NMR spectra using selective proton decoupling experiments allowed the conformation of the six membered ring to be established from vicinal coupling con

Transformations of quinic acid. Asymmetric synthesis and absolute configuration of mycosporin I and mycosporin-gly

D-(-)-Quinic acid (1) was converted to the fungal metabolites mycosporin I (2) and mycosporin-gly (13) via the iminophosphorane 64. The latter was prepared in 10 steps from 1 using oxidative bromination of quinide 33 to furnish 41. Reduction of the γ-lact

Diastereoselection and in Vivo inhibition of 3-dehydroquinate synthase

Epimeric carbaphosphonate [IR-(1α,3α,4β,5α)]-1,3,4-trihydroxy-5-(phosphonomethyl) cyclohexane-1-carboxylic acid and carbaphosphonate [1S-(1α,3β,4α,5β)]-1,3,4-trihydroxy-5-(phosphonomethyl) cyclohexane-1-carboxylic acid are potent inhibitors of purified 3-