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[会议论文] 作者:Pei-Qiang Huang, 来源:The 24th International Society of Heterocyclic Chemistry Con 年份:2013
[期刊论文] 作者:Hui Geng,Pei-Qiang Huang, 来源:中国化学:英文版 年份:2019
Summary of main observation and conclusion Direct functionalization of alkenes and direct transformation of carboxamides are two exciting areas that have attrac...
[期刊论文] 作者:Pei-Qiang Huang,Ying-Hong Huan, 来源:黑龙江科技学院学报 年份:2017
为探究吕家坨井田地质构造格局,根据钻孔勘探资料,采用分形理论和趋势面分析方法,研究了井田7...
[期刊论文] 作者:Shu-Ren Wang,Pei-Qiang Huang, 来源:黑龙江科技学院学报 年份:2019
为探究吕家坨井田地质构造格局,根据钻孔勘探资料,采用分形理论和趋势面分析方法,研究了井田7...
[期刊论文] 作者:Jiang-Feng Wu,Pei-Qiang Huang, 来源:中国化学快报(英文版) 年份:2020
The enantioselective total synthesis of the putative structure of versiquinazoline H and three diastereomers has been achieved, which allowed the revision of th...
[会议论文] 作者:Xiao Zheng,Pei-Qiang Huang, 来源:第十二届国际自由基化学会议(The 12th International Symposium on Organic Fr 年份:2016
[期刊论文] 作者:Pei-Qiang Huang,Wei Ou,Jian-Li, 来源:黑龙江科技学院学报 年份:2015
为探究吕家坨井田地质构造格局,根据钻孔勘探资料,采用分形理论和趋势面分析方法,研究了井田7...
[期刊论文] 作者:Pei-Qiang Huang Hui Geng Yong-, 来源:中国科学:化学英文版 年份:2015
(+)-preussin B 的第一 enantioselective 总数合成和抗真菌的碱(+)-preussin 的改进合成被描述。我们的途径依靠了在我们的实验室开发的四个步节俭的合成方法:(1 ) cis-diast...
[期刊论文] 作者:Xiao-Gang Wang,Ai-E Wang,Pei-Qiang Huang,, 来源:Chinese Chemical Letters 年份:2014
A short formal stereoselective synthesis of(-)-swainsonine(1) is described.Our synthesis started with the versatile building block(R)-3-benzyloxyglutarimide 5.T...
[期刊论文] 作者:Qi-Wei Lang,Xiu-Ning Hu,Pei-Qiang Huang,, 来源:Science China(Chemistry) 年份:2016
The direct partial reduction of highly stable secondary amides to more reactive aldimines and aldehydes is a challenging yet highly demanding transformation. In...
[期刊论文] 作者:Shi-Peng Luo,Xiong-Zhi Huang,Lian-Dong Guo,Pei-Qiang Huang, 来源:中国化学(英文版) 年份:2020
We describe the full details of our total synthesis of haliclonin A,a macrocyclic natural product suggest-ed to originate from a common biosynthetic intermediat...
[期刊论文] 作者:Ai-E Wang,Zong Chang,Yong-Peng Liu,Pei-Qiang Huang,, 来源:Chinese Chemical Letters 年份:2015
Secondary amides are a class of highly stable compounds serving as versatile starting materials,intermediates and directing groups(amido groups) in organic synt...
[期刊论文] 作者:Yan-Jiao Gao,Shi-Peng Luo,Jian-Liang Ye,Pei-Qiang Huang,, 来源:Chinese Chemical Letters 年份:2017
We describe the design and execution of a novel synthetic route to the tricyclic core of haliclonin A,a tetracyclic marine natural product.The approach features...
[会议论文] 作者:Zhi-Ping Yang,Qian He,Jian-Liang Ye,Pei-Qiang Huang, 来源:中国化学会第八届天然产物全合成青年学术研讨会 年份:2019
[会议论文] 作者:Jian-Liang Ye,Pan-Yuan Zhang,Pei-Qiang Huang,Xin Lu, 来源:The International Conference on Theory and Applications of C 年份:2008
[会议论文] 作者:Xiao Zheng,Xi-Jie Dai,Hong-Qiu Yuan,Jie Ma,Pei-Qiang Huang, 来源:The 24th International Society of Heterocyclic Chemistry Con 年份:2013
Recently, we have developed a novel titanocene-catalyzed radical cross-coupling reaction of hemiaminals with activated alkenes.Taking advantage of this new meth...
[会议论文] 作者:Jian-Liang Ye,Yu-Feng Zhang,Yang Liu,Jin-Yuan Zhang,Yuan-Ping Ruan,Pei-Qiang Huang, 来源:中国化学会第九届全国有机化学学术会议 年份:2015
[期刊论文] 作者:Feng-wei Li,Bo Zhou,Hang-zi Chen,Xue-li Bian,Qi-xu Cai,Yong-zhen Xing,Jian-ping He,Hongkui Zhang,Pei-qiang Huang, 来源:科学新闻 年份:2016
文章简介激活肿瘤细胞凋亡途径是临床治疗肿瘤的主要方法之一,但是长期的药物使用导致癌细胞对凋亡诱导产生抵抗。吴乔和林天伟实验室前期合作发现了小分子化合物THPN可以通...
[会议论文] 作者:Gulimiran Alitongbieke,Zhiping Zeng,Yue Ma,Mingfeng Huang,Hu Zhou,Gregory Cadwell,Jian-Feng Zheng,Pei-Qiang Huang, 来源:华东地区第十四届实验动物科学学术交流会 年份:2016
Retinoid X receptor-alpha (RXRα),an intriguing and unique drug target,can serve as an intracellular target mediating the anti-cancer effects of certain non-steroidal anti-inflammatory drugs (NSAIDs),i...
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