138513-22-1

Upstream product

• 138513-21-0 (1S,2R,3S,6R)-6-aminocyclohex-4-ene-1,2,3-triol 
• 138430-37-2 (1S,2R,3S,6R)-6-Benzyloxycarbonylamino-1,2-O-isopropylidenecyclohex-4-ene-1,2,3-triol 
• 86992-79-2 (1S,2S)-3-Chloro-cyclohexa-3,5-diene-1,2-diol 
• 138448-91-6 3-(benzyloxycarbonyl)-1-chloro-5,6-O-isopropylidene-2-oxa-3-azabicyclo<2.2.2>oct-7-ene-5,6-diol 
• 67451-62-1 cis-(1S,2S)-1,2-dihydroxy-3-bromocyclohexa-3,5-diene 
• 127666-06-2 (3aS,7aS)-4-chloro-2,2-dimethyl-3a,7a-dihydro-1,3-benzodioxole 
• 138145-77-4 (1S,4R,7S,8S)-(+)-7,8-O-Isopropylidenedioxy-2-oxa-3-azabicyclo<2.2.2>oct-5-ene hydrochloride 
• 137775-67-8 (1S,4R,5S,6R)-(-)-4-Amino-5,6-O-isopropylidenedioxycyclohex-2-en-1-ol 
• 80409-75-2 cis-2,2-dimethyl-3a,7a-dihydrobenzo[1,3]dioxole 
• 138448-92-7 3-(benzyloxycarbonyl)-1-bromo-5,6-O-isopropylidene-2-oxa-3-azabicyclo<2.2.2>oct-7-ene-5,6-diol 
• 130669-75-9 (3aS,7aS)-4-bromo-2,2-dimethyl-3a,7a-dihydro-1,3-benzodioxole 
• 138430-40-7 (1S,2R,3S,6R)-6-Benzyloxycarbonylaminocyclohex-4-ene-1,2,3-triol 

Downstream Products

• 123808-78-6 (1S,2R,3S,4R)-(+)-4-Acetamidocyclohexane-1,2,3-triyl triacetate 

Relevant academic research and scientific papers

Asymmetric Synthesis of cis-1,3-Diamino-1,3-dideoxycyclitols

Starting with the hetero-Diels-Alder reaction of the O-isopropylidene-protected cis-cyclohexa-3,5-diene-1,2-diol with (-)-2,3:5,6-di-O-isopropylidene-1-nitroso-α-D-manno-furanosyl chloride the optically pure (+)-endo-adduct was exclusively formed.After re

Biocatalysis as the Strategy of Choice in the Exhaustive Enantiomerically Controlled Synthesis of Conduritols

An approach to several conduritols, both naturally occurring and unnatural derivatives, is described.The key strategy of this potentially exhaustive approach relies on the bio-oxidation of chloro- or bromo-benzene to their corresponding cis-diols.Subseque

Stereospecific synthesis of aminocyclitols via cycloadditions of unsymmetrical, optically pure dienes: Conduramine A-1 and Dihydroconduramine A-1

Stereospecific synthesis of Conduramine A-1 and Dihydroconduramine A-1 has been achieved by a fully regio- and stereospecific hetero Diels-Alder cycloaddition of a nitrosyl derivative and homochiral 1-halocyclohexadiene diols obtained by microbial oxidati