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Biomimetic Asymmetric Synthesis of (R)-GTRI-02 and (3S,4R)-3,4-Dihydroxy-3,4-dihydronaphthalen-1(2H)-ones

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Figshare2016-02-20 更新2026-04-29 收录
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https://figshare.com/articles/dataset/Biomimetic_Asymmetric_Synthesis_of_i_R_i_GTRI_02_and_3_i_S_i_4_i_R_i_3_4_Dihydroxy_3_4_dihydronaphthalen_1_2_i_H_i_ones/2503510
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The NADPH-dependent tetrahydroxynaphthalene reductase (T4HNR) from Magnaporthe grisea was used for the biomimetic synthesis of (R)-GTRI-02 by stereoselective reduction of 1-(3,6,8-trihydroxy-1-methylnaphthalen-2-yl)ethanone. This also led to the isolation of a (3S,4R)-cis-ketodiol formed by T4HNR-catalyzed reduction of the corresponding hydroxynaphthoquinone. Flaviolin and lawsone also reduced to corresponding cis-ketodiols in good yields.
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2016-02-20
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