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Synthesis of single stereoisomers of 2,2-disubstituted 3-hydroxycyclohexane-1-ones via enzymatic desymmetric reduction of the 1,3-cyclohexanediones
Green Synthesis and Catalysis ( IF 8.2 ) Pub Date : 2021-8-27 , DOI: 10.1016/j.gresc.2021.04.009 Liangyan Zhu , Yunfeng Cui , Xi Chen , Hongliu Zhang , Jinhui Feng , Qiaqing Wu , Dunming Zhu
Green Synthesis and Catalysis ( IF 8.2 ) Pub Date : 2021-8-27 , DOI: 10.1016/j.gresc.2021.04.009 Liangyan Zhu , Yunfeng Cui , Xi Chen , Hongliu Zhang , Jinhui Feng , Qiaqing Wu , Dunming Zhu
Chiral cyclic 3-hydroxy ketones are widely used as building blocks in the
synthesis of natural products and bioactive compounds. Through screening
the carbonyl reductases, the chiral cyclic 3-hydroxy hexane-1-one products
bearing an all-carbon chiral quaternary center could be obtained with high
enantioselectivities (up to 99% ee ) and diastereoselectivities (up to 99:1 dr).
中文翻译:
通过 1,3-环己烷二酮的酶促去对称还原合成 2,2-二取代的 3-羟基环己烷-1-酮的单一立体异构体
手性环状 3-羟基酮被广泛用作合成天然产物和生物活性化合物的构建单元。通过羰基还原酶的筛选,可以得到具有高对映选择性(高达 99% ee )和非对映选择性(高达 99:1 dr)的具有全碳手性季铵中心的手性环状 3-羟基己烷-1-one 产物。
更新日期:2021-09-29
中文翻译:
通过 1,3-环己烷二酮的酶促去对称还原合成 2,2-二取代的 3-羟基环己烷-1-酮的单一立体异构体
手性环状 3-羟基酮被广泛用作合成天然产物和生物活性化合物的构建单元。通过羰基还原酶的筛选,可以得到具有高对映选择性(高达 99% ee )和非对映选择性(高达 99:1 dr)的具有全碳手性季铵中心的手性环状 3-羟基己烷-1-one 产物。