Synthetic studies of an 18-membered antitumor macrolide, tedanolide. 6. Synthesis of a key intermediate via a highly efficient macrolactonization of computer-aid designed seco-acid.

Matsushima T; Nakajima N; Zheng BZ; Yonemitsu O

首页> 外文期刊>Chemical and Pharmaceutical Bulletin >Synthetic studies of an 18-membered antitumor macrolide, tedanolide. 6. Synthesis of a key intermediate via a highly efficient macrolactonization of computer-aid designed seco-acid.

【24h】

Synthetic studies of an 18-membered antitumor macrolide, tedanolide. 6. Synthesis of a key intermediate via a highly efficient macrolactonization of computer-aid designed seco-acid.

机译：十八元抗肿瘤大环内酯泰达内酯的合成研究。 6.通过计算机辅助设计的癸二酸的高效大内酯化合成关键中间体。

获取原文

获取原文并翻译 | 示例

掌桥外文数据库（机构版） >>

开具论文收录证明 >>

文献代查 >>

页面导航

著录项
相似文献
相关主题

著录项

来源
《Chemical and Pharmaceutical Bulletin》 |2000年第6期|共6页
作者
Matsushima T; Nakajima N; Zheng BZ; Yonemitsu O;
展开▼
作者单位

展开▼
收录信息
原文格式 PDF
正文语种 eng
中图分类药学;化学;
关键词
Antineoplastic Agents; Macrolides; 抗肿瘤药; 大环内酯类;

机译：Antineoplastic Agents;Macrolides;抗肿瘤药;大环内酯类;

相似文献

外文文献
中文文献
专利

1. Synthetic studies of an 18-membered antitumor macrolide, tedanolide. 6. Synthesis of a key intermediate via a highly efficient macrolactonization of computer-aid designed seco-acid. [J] . Matsushima T, Nakajima N, Zheng BZ, Chemical and Pharmaceutical Bulletin . 2000,第6期

机译：十八元抗肿瘤大环内酯泰达内酯的合成研究。 6.通过计算机辅助设计的癸二酸的高效大内酯化合成关键中间体。
2. Synthetic Studies of 18-Membered Antitumor Macrolide, Tedanolide. 2. Stereoselective Synthesis of the C1-C7 Fragment via a Mismatched but Highly Efficient Sharpless Dihydroxylation [J] . Tomohiro Matsushima, Michiko Mori, Noriyuki Nakajima, Chemical and Pharmaceutical Bulletin . 1998,第7期

机译：十八元抗肿瘤大环内酯泰达内酯的合成研究。 2.通过不匹配但高效的无尖锐二羟基化立体选择性合成C1-C7片段
3. Synthetic studies of the 18-membered antitumor macrolide, tedanolide. 3. Stereocontrolled synthesis of the C1-C12 part via a synthesis of the C1-C7 fragment by a mismatched but efficient sharpless dihydroxylation and its coupling with the C8-C11 frag [J] . Matsushima T, Mori M, Zheng BZ, Chemical and Pharmaceutical Bulletin . 1999,第3期

机译：18元抗肿瘤大环内酯泰达内酯的合成研究。 3.通过不匹配但有效的无尖锐二羟基化合成C1-C7片段及其与C8-C11碎片的立体控制的C1-C12片段的合成
4. Highly-Efficient Preparation of Key Intermediate of Huperzine A [C] . Xie Kai-ming International Conference on Green Power, Materials and Manufacturing Technology and Applications . 2014

机译：高效制备Huperzine A的关键中间体
5. Part I: Total Synthesis of Marine Macrolide Amphidinolide F and Synthetic Studies Toward Amphidinolide C; Part II: Computational Study on Proline Sulfonamide-catalyzed Aldol Reaction. [D] . Mahapatra, Subham. 2013

机译：第一部分：海洋大环内酯Amphidinolide F的全合成及对Amphidinolide C的合成研究；第二部分：脯氨酸磺酰胺催化的羟醛反应的计算研究。
6. Efficient Synthesis of THP/THF-Containing Macrolides via Palladium-Catalyzed Alkoxycarbonylative Macrolactonizations [O] . Yu Bai, Dexter C. Davis, Mingji Dai -1

机译：通过钯催化的烷氧羰基化大内酯化法高效合成含THP / THF的大环内酯
7. Synthetic Studies of an 18-Membered Antitumor Macrolide, Tedanolide. 6. Synthesis of a Key Intermediate via a Highly Efficient Macrolactonization of Computer-Aid Designed Seco-Acid. [O] . Tomohiro MATSUSHIMA, Noriyuki NAKAJIMA, Bao-Zhong ZHENG, 2000

机译：18元抗肿瘤大环内酯，鸡醇苷的合成研究。 6.通过高效的计算机辅助型Seco-acid的高效宏酰胺化合成关键中间体。

Synthetic studies of an 18-membered antitumor macrolide, tedanolide. 6. Synthesis of a key intermediate via a highly efficient macrolactonization of computer-aid designed seco-acid.

著录项

相似文献

相关主题

期刊订阅