Recherches dans la série des cyclitols XIII. Préparation et oxydation biochimique du<i>d</i>-viburnitol
作者:Théodore Posternak
DOI:10.1002/hlca.19500330627
日期:——
L'hydrogénation catalytique du d-inosose en milieu fortement acide fournit du d-viburnitol. Sous l'action d'Acetobacter suboxydans, les d- et l-viburnitols se transforment en deux tétrahydroxy-cyclohexanones énantiomorphes.
L'氢化catalytique杜d -inosose烯环境fortement酸fournit杜d -viburnitol。苏L'行动d'醋酸菌,LES d -等升-viburnitols SE transforment EN德塞夫勒四羟基-环己酮énantiomorphes。
2-deoxy-scyllo-inosose reductase
申请人:Asahi Kasei Chemicals Corporation
公开号:US10000743B2
公开(公告)日:2018-06-19
The disclosure provides 2-deoxy-scyllo-inosose reductases derived from a microorganism having the ability to utilize (−)-vibo-quercitol, recombinant vectors and transformants comprising genes encoding the same, and methods of use thereof.
Photooxygenation of 1,4-cyclohexadiene 3 followed by reduction with LiAlH4 or thiourea gave (25/1)-cyclohex-3-ene-triol 7a. trans-Hydroxylation of triol 7a with three different methods afforded both of proto-quercitol la and vibo-quercitol 2a.
Cambie, Richard C.; Renner, Noel D.; Rutledge, Peter S., Australian Journal of Chemistry, 1990, vol. 43, p. 1597 - 1602
作者:Cambie, Richard C.、Renner, Noel D.、Rutledge, Peter S.、Woodgate, Paul D.