Study on highly diastereoselective synthesis of (2'R)-2'-deoxy[2'-2H]guanosine.

E Kawashima, Y S Terui, Y Ishido, K Yokozeki
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引用次数: 0

Abstract

To develop an efficient method for the synthesis of a highly diasteroselective (2'R)-2'-deoxy[2'-2H]guanosine (1), studies of organic chemical conversion from 2'-bromo-2'-deoxy-N2-Isobutyryl-3',5'-O-TIPDS-guanosine (2) to 1 and a biological transdeoxyribofuranosylation of (2'R > 98% de)-2'-deoxy[2'-2H]uridine (4) were carried out. As the results, a highly diastereoselective synthesis of 1 was achieved by a biological transdeoxyribofuranosylation between 2,6-diaminopurine and 4 by the use of Enterobacter aerogenes AJ-11125, followed by treatment with adenosine deaminase. The results will be described in detail.

高度非对映选择性合成(2' r)-2'-脱氧[2'-2H]鸟苷的研究。
为了开发一种高效合成高非对映选择性(2' r)-2'-脱氧[2'-2H]鸟苷(1)的方法,研究了2'-溴-2'-脱氧- n2 -异丁基-3',5'- o- tipds -鸟苷(2)到1的有机化学转化和(2' r > 98% de)-2'-脱氧[2'-2H]尿苷(4)的生物转脱氧核呋喃基化。结果表明,利用产气肠杆菌AJ-11125在2,6-二氨基嘌呤和4之间进行生物转脱氧核呋喃基化,然后用腺苷脱氨酶处理,实现了1的高度非对构选择性合成。结果将被详细描述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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