Total synthesis of cyanolide A | |
Department | 羰基合成与选择氧化国家重点实验室 |
Yang Z(杨震); Xie XG(谢新刚); Jing P(靖鹏); Zhao GY(赵高原); Zheng JY(郑计岳); Zhao CG(赵常贵); She XG(厍学功) | |
2011 | |
Source Publication | Org. Biomol. Chem. |
ISSN | 1477-0520 |
Volume | 9Pages:984-986 |
Abstract | The total synthesis of cyanolide A has been achieved in 14 steps fromcommercially available (S)-2-ethyloxirane, exploiting the palladium-catalyzed intramolecular alkoxycarbonylation as the key step to construct the tetrasubstituted cistetrahydropyran ring with high stereoselectivity. |
Subject Area | 物理化学 |
Funding Organization | the MOST (2010CB833200);the NSFC (20872054;20732002);program 111 |
Indexed By | SCI |
Language | 英语 |
Citation statistics | |
Document Type | 期刊论文 |
Identifier | http://ir.licp.cn/handle/362003/396 |
Collection | 羰基合成与选择氧化国家重点实验室(OSSO) |
Corresponding Author | She XG(厍学功) |
Recommended Citation GB/T 7714 | Yang Z,Xie XG,Jing P,et al. Total synthesis of cyanolide A[J]. Org. Biomol. Chem.,2011,9:984-986. |
APA | 杨震.,谢新刚.,靖鹏.,赵高原.,郑计岳.,...&厍学功.(2011).Total synthesis of cyanolide A.Org. Biomol. Chem.,9,984-986. |
MLA | 杨震,et al."Total synthesis of cyanolide A".Org. Biomol. Chem. 9(2011):984-986. |
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