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19.
Hiroshi Ohrui Tsutami Misawa Hiroshi Meguro 《Bioscience, biotechnology, and biochemistry》2013,77(7):1825-1829
The photobromination of 1,5-anhydro-2,3-O-isopropylidene-β-d-ribofuranose gave the corresponding (5S)-5-bromo compound. The reduction of the bromide with triphenyltindeuteride gave (5S)-(5-2H1)-1,5-anhydro-2,3-O-isopropylidene-β-d-ribofuranose, with a chiral purity of 76% at C-5, which was converted to (5R)- and (5S)-(5-2H1)-d-riboses and other ribofuranose derivatives. 相似文献
20.
E. N. Kalinichenko V. N. Barai S. B. Bokut V. V. Romanova A. I. Zinchenko G. Herrmann I. A. Mikhailopulo 《Biotechnology letters》1989,11(9):621-626
Summary The title compounds were prepared by an enzymatic transdeoxyribosylation from 2 dGuo or 2 dThd to the respective heterocyclic bases, 5-ethyluracil and (E)-5-(2-bromovinyl)uracil, using the whole bacterial cells ofEscherichia coli as a biocatalyst. 相似文献