KIB OpenIR

浏览/检索结果: 共21条,第1-10条 帮助

限定条件        
已选(0)清除 条数/页:   排序方式:
Two anti-inflammatory chlorinated azaphilones from Chaetomium globosum TW1-1 cultured with 1-methyl-L-tryptophan and structure revision of chaephilone C 期刊论文
TETRAHEDRON LETTERS, 2020
作者:  Gao, Weixi;  Chai, Chenwei;  Li, Xiao-Nian;  Sun, Weiguang;  Li, Fengli;  Chen, Chunmei;  Wang, Jianping;  Zhu, Hucheng;  Wang, Yanyan;  Hu, Zhengxi;  Zhang, Yonghui
浏览  |  Adobe PDF(499Kb)  |  收藏  |  浏览/下载:97/39  |  提交时间:2021/01/05
Stereocontrolled concise synthesis of (+/-)-halosaline through intramolecular C-H amination 期刊论文
TETRAHEDRON LETTERS, 2019, 卷号: 60, 期号: 27, 页码: 1781-1783
作者:  Meng, Chun-Yan;  Liang, Xiao;  Zhang, Hongbin;  Wei, Kun;  Yang, Yu-Rong
浏览  |  Adobe PDF(482Kb)  |  收藏  |  浏览/下载:165/41  |  提交时间:2019/08/19
C-H amination  Halosaline  Ring-closing metathesis  Total synthesis  
Macahydantoins A and B, two new thiohydantoin derivatives from Maca (Lepidium meyenii): Structural elucidation and concise synthesis of macahydantoin A 期刊论文
TETRAHEDRON LETTERS, 2017, 卷号: 58, 期号: 17, 页码: 1684-1686
作者:  Yu, Mu-Yuan;  Qin, Xu-Jie;  Shao, Li-Dong;  Peng, Xing-Rong;  Li, Lei;  Yang, Han;  Qiu, Ming-Hua
Adobe PDF(537Kb)  |  收藏  |  浏览/下载:189/39  |  提交时间:2017/08/29
Cruciferae  Lepidium Meyenii  Thiohydantoin Derivatives  Concise Synthesis  
Two key biogenetic intermediates of Cephalotaxus alkaloids from Cephalotaxus oliveri and C. lanceolata 期刊论文
TETRAHEDRON LETTERS, 2016, 卷号: 57, 期号: 47, 页码: 5201-5204
作者:  Ni, Ling;  Schinnerl, Johann;  Bao, Mei-fen;  Zhang, Bing-jie;  Wu, Jing;  Cai, Xiang-hai
Adobe PDF(953Kb)  |  收藏  |  浏览/下载:218/48  |  提交时间:2017/01/05
Cephalotaxus Oliveri  Cephalotaxus Lanceolata  (+/-)-cephaloliverine a  Cephalolancine a  Biogenetic Intermediates  
Speramides A-B, two new prenylated indole alkaloids from the freshwater-derived fungus Aspergillus ochraceus KM007 期刊论文
TETRAHEDRON LETTERS, 2016, 卷号: 57, 期号: 45, 页码: 4952-4955
作者:  Chang, Yao-Wen;  Yuan, Chun-Mao;  Zhang, Jing;  Liu, Shuai;  Cao, Pei;  Hua, Hui-Ming;  Di, Ying-Tong;  Hao, Xiao-Jiang
Adobe PDF(866Kb)  |  收藏  |  浏览/下载:307/63  |  提交时间:2017/01/05
Speramide  Brevianamide  Prenylated Indole Alkaloid  Aspergillus Ochraceus  Notoamide  
Three new alkaloids from Myrioneuron faberi 期刊论文
TETRAHEDRON LETTERS, 2016, 卷号: 57, 期号: 36, 页码: 4021-4023
作者:  Cao, Ming-Ming;  Zhang, Yu;  Huang, Sheng-Dian;  Peng, Zong-Gen;  Jiang, Jian-Dong;  Hao, Xiao-Jiang
Adobe PDF(643Kb)  |  收藏  |  浏览/下载:317/92  |  提交时间:2016/11/04
Myrioneuron Alkaloids  Lysine-based Alkaloids  Anti-hcv Activity  
Alstorisine A, a nor-monoterpenoid indole alkaloid from cecidogenous leaves of Alstonia scholaris 期刊论文
TETRAHEDRON LETTERS, 2016, 卷号: 57, 期号: 16, 页码: 1754-1757
作者:  Chen, Ying-Ying;  Yang, Jing;  Yang, Xing-Wei;  Khan, Afsar;  Liu, Lu;  Wang, Bei;  Zhao, Yun-Li;  Liu, Ya-Ping;  Ding, Zhong-Tao;  Luo, Xiao-Dong
Adobe PDF(679Kb)  |  收藏  |  浏览/下载:363/70  |  提交时间:2016/08/22
Alstonia Scholaris  Galls  Monoterpenoid Indole Alkaloid  Absolute Configuration  
Alstoscholarisines F and G, two unusual monoterpenoid indole alkaloids from the leaves of Alstonia scholaris 期刊论文
TETRAHEDRON LETTERS, 2015, 卷号: 56, 期号: 48, 页码: 6715-6718
作者:  Yang,Xing-Wei;  Song,Chang-Wei;  Zhang,Yu;  Khan,Afsar;  Jiang,Li-Ping;  Chen,Yong-Bin;  Liu,Ya-Ping;  Luo,Xiao-Dong
Adobe PDF(698Kb)  |  收藏  |  浏览/下载:231/57  |  提交时间:2016/01/19
Monoterpenoid Indole Alkaloid  Alstonia Scholaris  Alstoscholarisines f And g  Absolute Configuration  
Iridium-catalyzed enantioselective synthesis of (-)- and (+)-aurantioclavine 期刊论文
TETRAHEDRON LETTERS, 2015, 卷号: 56, 期号: 43, 页码: 5933-5936
作者:  Lei,Ting;  Zhang,Hongbin;  Yang,Yu-Rong
Adobe PDF(660Kb)  |  收藏  |  浏览/下载:174/60  |  提交时间:2016/01/19
Iridium-catalyzed  Asymmetric Amination  Aurantioclavine  
Asymmetric synthesis of common aza-tricyclic core of various alkaloids 期刊论文
TETRAHEDRON LETTERS, 2015, 卷号: 56, 期号: 40, 页码: 5460-5464
作者:  Ding,Ming;  Tong,Xiaogang;  Li,Dashan;  Liang,Kangjiang;  Zhou,Ankun;  Zuo,Zhili;  Xia,Chengfeng
Adobe PDF(761Kb)  |  收藏  |  浏览/下载:180/41  |  提交时间:2016/01/19
Alkaloid  Asymmetric  Cyclization  Natural Product  Synthesis