首页> 外文OA文献 >Synthesis of Methyl-substituted Bicyclic Carbanucleoside Analogs as Potential Antiherpetic Agents

【2h】

Synthesis of Methyl-substituted Bicyclic Carbanucleoside Analogs as Potential Antiherpetic Agents

机译：甲基取代的双环核苷类似物的合成潜在的耐助药剂

代理获取

本网站仅为用户提供外文OA文献查询和代理获取服务，本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文，但由于OA文献来源多样且变更频繁，仍可能出现获取不到、文献不完整或与标题不符等情况，如果获取不到我们将提供退款服务。请知悉。

页面导航

著录项
引文网络
相似文献
相关主题

著录项

作者

展开▼
作者单位

展开▼
年度 2008
总页数
原文格式 PDF
正文语种
中图分类

相似文献

外文文献
中文文献
专利

1. Synthesis of Methyl-substituted Bicyclic Carbanucleoside Analogs as Potential Antiherpetic Agents [J] . Kyung Ran Kim, Ah-Young Park, Hyung-Rock Lee Bulletin of the Korean Chemical Society . 2008,第10期

机译：甲基取代的双环碳核苷类似物的合成作为潜在的抗疱疹药
2. Synthesis of Methyl-substituted Bicyclic Carbanucleoside Analogs as Potential Antiherpetic Agents [J] . Ah Young Park, Hyung Rock Lee, Hyung Ryong Moon, Bulletin of the Korean Chemical Society . 2008,第10期

机译：甲基取代的双环碳核苷类似物的合成作为潜在的抗疱疹药
3. Stereoselective synthesis of 2 '-C-methyl-cyclopropyl-fused carbanucleosides as potential anti-HCV agents [J] . Lee JA, Kim HO, Tosh DK, Organic letters . 2006,第22期

机译：立体选择性合成2'-C-甲基-环丙基-融合的碳核苷作为潜在的抗HCV药物
4. Synthesis and toxicological activity of 5-nitroindazole sulfonamides derivatives as potential antimicrobial agents. Optimization of the synthesis [C] . Corina Cheptea, Andreea-Celia Benchea, Marius Găină, 2017 E-Health and Bioengineering Conference . 2017

机译：5-硝基吲唑磺酰胺衍生物作为潜在抗菌剂的合成及其毒理活性。优化合成
5. Part I. Asymmetric synthesis of bicyclic analogues of risedronate as molecular probes of the mechanism of action of bisphosphonate antiosteoporotic drugs and potentially more efficacious antiosteoporotic agents. Part II. Facile preparation and functionalization of chiral stabilized ylides from common chiral auxiliaries using the Bestmann ylide and their use in Wittig reactions. Part III. Asymmetric organocatalysis: 1. An investigation of alpha-hydroxylation of aldehydes; 2. Synthesis of a novel camphor-based alpha-aminotetrazole organocatalyst. [D] . Song, Xinyi. 2007

机译：第一部分：利塞膦酸盐双环类似物的不对称合成，作为双膦酸盐类抗骨质疏松药和潜在更有效的抗骨质疏松药作用机理的分子探针。第二部分使用Bestmann内酯从常见手性助剂轻松制备和官能化手性稳定化的叶基及其在Wittig反应中的用途。第三部分不对称有机催化：1.醛的α-羟基化研究； 2.合成新的基于樟脑的α-氨基四唑有机催化剂。
6. Antitumor Agents 250. Design and Synthesis of New Curcumin Analogs as Potential Anti-Prostate Cancer Agents [O] . Li Lin, Qian Shi, Alexander K. Nyarko, -1

机译：抗肿瘤药250.设计和合成新的姜黄素类似物作为潜在的抗前列腺癌药物
7. Synthesis of Simplified Azasordarin Analogs as Potential Antifungal Agents [O] . Yibiao Wu, Chris Dockendorff 2019

机译：简体氮杂胆蛋白类似物的合成潜在的抗真菌剂
8. Synthesis of Bicyclic Polyhalogeno Compounds and New Heterocyclics Containing S, Hg or As with Polyhalogen Side Chains as Potential Antimalarial Agents. [R] . Park, J. D. 1970

机译：双环多卤代化合物和含有s，Hg或as的新杂环化合物与多卤素侧链作为潜在的抗疟药。

Synthesis of Methyl-substituted Bicyclic Carbanucleoside Analogs as Potential Antiherpetic Agents

著录项

引文网络

相似文献

相关主题

期刊订阅