LICP OpenIR  > 羰基合成与选择氧化国家重点实验室(OSSO)
Facile total synthesis of the antimalarial nonenolide
Department羰基合成与选择氧化国家重点实验室
Liu J(刘剑); Zhang L(张玲); He JM(何金梅); He LE(何六二); Ma BW(马博文); Pan XF(潘鑫复); She XG(厍学功)
2008
Source PublicationTetrahedron: Asymmetry
ISSN0957-4166
Volume19Pages:906-911
AbstractThe facile total synthesis of the antimalarial nonenolide 1 is reported. The convergent strategy features the use of reactions such as Sharpless asymmetric dihydroxylation, aldol addition, Mitsunobu reaction, and ring-closing metathesis (RCM).
Subject Area物理化学
Funding Organizationthe Special Doctorial Program Funds of the Ministry of Education of China (20040730008);NSFC (QT Program, No. 20572037);NCET-05-0879;the key grant project of Chinese Ministry of Education (No. 105169);the Gansu Science Foundation (3ZS051-A25-004)
Indexed BySCI
Language英语
Citation statistics
Cited Times:25[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/1917
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
Liu J,Zhang L,He JM,et al. Facile total synthesis of the antimalarial nonenolide[J]. Tetrahedron: Asymmetry,2008,19:906-911.
APA 刘剑.,张玲.,何金梅.,何六二.,马博文.,...&厍学功.(2008).Facile total synthesis of the antimalarial nonenolide.Tetrahedron: Asymmetry,19,906-911.
MLA 刘剑,et al."Facile total synthesis of the antimalarial nonenolide".Tetrahedron: Asymmetry 19(2008):906-911.
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