138448-91-6

Upstream product

• 3426-71-9 Benzyl N-hydroxycarbamate 
• 127666-06-2 (3aS,7aS)-4-chloro-2,2-dimethyl-3a,7a-dihydro-1,3-benzodioxole 
• 86992-79-2 (1S,2S)-3-Chloro-cyclohexa-3,5-diene-1,2-diol 

Downstream Products

• 138513-22-1 dihydroconduramine A-1 
• 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 

Relevant academic research and scientific papers

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

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