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Enantioselective total syntheses of slagenins A-C and their antipodes
Alternative Titleslagenins A-C及其对映体的对映选择性合成
Jiang B(姜标); Liu JF(刘家峰); Zhao SY(赵圣印)
2003
Source PublicationJ. Org. Chem.
ISSN0022-3263
Volume68Issue:6Pages:2376-2384
AbstractFull details of the total syntheses of slagenins A-C(1a-c) and their antipodes (2a-c), novel bromopyrrole alkaloids with a unique tertrahydrofuro[2,3-d]imidazolidin-2-one moiety, are described in which their absolute stereochemistry was established. The key step in the syntheses involves the efficient condensation of dihydrofuran-3-one or glyoxal with urea to construct the slagenin bicycle core
Subject Area天然产物有机化学
Department中国科学院上海有机化学研究所金属有机化学开放实验室
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Indexed BySCI
Language英语
WOS IDWOS:000181639300042
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Document Type期刊论文
Identifierhttp://ir.sioc.ac.cn/handle/331003/20183
Collection中科院天然产物有机化学重点实验室
Corresponding AuthorJiang B(姜标)
Recommended Citation
GB/T 7714
Jiang B,Liu JF,Zhao SY. Enantioselective total syntheses of slagenins A-C and their antipodes[J]. J. Org. Chem.,2003,68(6):2376-2384.
APA 姜标,刘家峰,&赵圣印.(2003).Enantioselective total syntheses of slagenins A-C and their antipodes.J. Org. Chem.,68(6),2376-2384.
MLA 姜标,et al."Enantioselective total syntheses of slagenins A-C and their antipodes".J. Org. Chem. 68.6(2003):2376-2384.
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