138448-92-7

Upstream product

• 3426-71-9 Benzyl N-hydroxycarbamate 
• 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 
• 108-86-1 bromobenzene 

Downstream Products

• 144347-50-2 (6-Bromo-benzo[1,3]dioxole-5-carbonyl)-[(3aS,4S,7R,7aS)-7-(isopropyl-dimethyl-silanyloxy)-2,2-dimethyl-3a,4,7,7a-tetrahydro-benzo[1,3]dioxol-4-yl]-carbamic acid benzyl ester 
• 144347-51-3 (3aS,3bS,12R,12aS)-12-(Isopropyl-dimethyl-silanyloxy)-2,2-dimethyl-5-oxo-3a,5,12,12a-tetrahydro-3bH-1,3,7,9-tetraoxa-4-aza-dicyclopenta[a,h]phenanthrene-4-carboxylic acid benzyl ester 
• 144347-53-5 [(3aS,4S,7R,7aS)-7-(Isopropyl-dimethyl-silanyloxy)-2,2-dimethyl-3a,4,7,7a-tetrahydro-benzo[1,3]dioxol-4-yl]-carbamic acid benzyl ester 
• 138430-37-2 (1S,2R,3S,6R)-6-Benzyloxycarbonylamino-1,2-O-isopropylidenecyclohex-4-ene-1,2,3-triol 
• 138430-39-4 ((3aS,4R,7aS)-2,2-Dimethyl-7-oxo-3a,4,7,7a-tetrahydro-benzo[1,3]dioxol-4-yl)-carbamic acid benzyl ester 
• 138430-37-2 ((3aS,4S,7R,7aR)-7-Hydroxy-2,2-dimethyl-3a,4,7,7a-tetrahydro-benzo[1,3]dioxol-4-yl)-carbamic acid benzyl ester 
• 138430-40-7 (1S,2R,3S,6R)-6-Benzyloxycarbonylaminocyclohex-4-ene-1,2,3-triol 
• 138513-22-1 dihydroconduramine A-1 
• 123808-78-6 (1S,2R,3S,4R)-(+)-4-Acetamidocyclohexane-1,2,3-triyl triacetate 

Relevant academic research and scientific papers

Microbial oxidation of aromatics in enantiocontrolled synthesis. 3.1 design of amino cyclitols (exo-nitrogenous) and total synthesis of (+)-lycoricidine via acylnitrosyl cycloaddition to polarized 1-halo-1,3-cyclohexadienes

Oxidation of halogenated benzenes with bacterial dioxygenase from Pseudomonas putida 39D (whole cell fermentation) provided homochiral 1,3-cyclohexadiene-cis-diols 1 for the entire halogen series. These compounds were investigated for their potential in c

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

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