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[天然存在的含氮杂环化合物43年化学研究亮点。(2). 嘌呤及其核苷的合成与反应]

[Highlights from 43 years of chemistry of naturally occurring nitrogen-containing heterocycles. (2). Syntheses and reactions of purines and of their nucleosides].

作者信息

Fujii T, Ito N

机构信息

Faculty of Pharmaceutical Sciences, Kanazawa University, Japan.

出版信息

Yakugaku Zasshi. 1996 May;116(5):355-73. doi: 10.1248/yakushi1947.116.5_355.

Abstract

The studies on the syntheses and reactions of purines and their nucleosides, carried out by the present author's group for these 34 years, are reviewed with particular emphasis on the employed synthetic strategies and tactics. Among the studies included in this review are as follows: ring-opening and recyclization of the adenine ring utilizing an N(1)-alkoxy group; kinetic studies of the Dimroth rearrangement and related reactions in the adenine series; syntheses and reactions of new Nx,Ny-disubstituted adenines and of new Nx-substituted adenosines; syntheses, structure determinations, and structure-activity relationships of new natural cytokinins; syntheses and reactions of new marine 8-oxopurines; syntheses, reactions, and biological activities of the N(7)-oxides of guanine, hypoxanthine, adenine, 6-mercaptopurine, and 6-methylthiopurine.

摘要

本文作者团队在过去34年中对嘌呤及其核苷的合成与反应进行了研究,现对此进行综述,特别强调所采用的合成策略和方法。本综述涵盖的研究包括:利用N(1)-烷氧基对腺嘌呤环进行开环和环化;腺嘌呤系列中迪姆罗特重排及相关反应的动力学研究;新型Nx,Ny-二取代腺嘌呤和新型Nx-取代腺苷的合成与反应;新型天然细胞分裂素的合成、结构测定及构效关系;新型海洋8-氧代嘌呤的合成与反应;鸟嘌呤、次黄嘌呤、腺嘌呤、6-巯基嘌呤和6-甲基硫代嘌呤的N(7)-氧化物的合成、反应及生物活性。

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