β-Selective D-Psicofuranosylation of Pyrimidine Bases and Thiols
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N-Glycosidation of D-psicofuranosyl donor 1 with pyrimidine bases took place β-selectively in a β/α-ratio of 8:1 ~ 7:1. For S-glycosidation, 3,4-O-(3-pentylidene)-protected D-psicofuranosyl donor 15 was effective to increase β-selectivity up to 7:1.
HETEROCYCLES, 97(2), pp.729-743; 2018
収録刊行物
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- HETEROCYCLES
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HETEROCYCLES 97 (2), 729-743, 2018-03-05
日本複素環化学研究所
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詳細情報 詳細情報について
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- CRID
- 1050287297252297728
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- NII論文ID
- 120006987688
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- NII書誌ID
- AA00663739
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- ISSN
- 03855414
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- HANDLE
- 10069/39288
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- NDL書誌ID
- 029624978
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- 本文言語コード
- en
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- 資料種別
- journal article
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- データソース種別
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