LICP OpenIR  > 羰基合成与选择氧化国家重点实验室(OSSO)
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 PublicationOrg. Biomol. Chem.
ISSN1477-0520
Volume9Pages:984-986
AbstractThe 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 Organizationthe MOST (2010CB833200);the NSFC (20872054;20732002);program 111
Indexed BySCI
Language英语
Citation statistics
Cited Times:32[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://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 AuthorShe 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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