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Synthetic Studies toward Parvistemoline Using Asymmetric Ir/Amine-Catalyzed Allylation
Zheng,Yu; Yang,Hong-Dou; Wei,Kun; Yang,Yu-Rong
2021
发表期刊JOURNAL OF ORGANIC CHEMISTRY
ISSN0022-3263
卷号86期号:8页码:6025-6029
摘要The common, key tricyclic core of stemona alkaloids parvistemonine (1) and parvistemoline (2), whose synthetic efforts have not reported yet, was constructed through a new strategy in which three contiguous stereogenic centers were set by using Carreira's asymmetric Ir/amine-catalyzed allylation of aldehyde with alpha-vinylfurfuryl alcohol and Ellman's sulfinamide chiral auxiliary, respectively. The furan ring was especially designed to act as the precursor of the butyrolactone while establishing the significant chirality.
关键词ENANTIOSELECTIVE TOTAL-SYNTHESIS ALPHA-ALLYLATION STEMONA ALKALOIDS IRIDIUM
DOI10.1021/acs.joc.1c00390
WOS记录号WOS:000641292800054
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文献类型期刊论文
条目标识符http://ir.kib.ac.cn/handle/151853/73224
专题中国科学院昆明植物研究所
作者单位1.[Zheng, Yu
2.Yang, Hong-Dou
3.Wei, Kun
4.Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources West Ch, Kunming 650201, Yunnan, Peoples R China
5.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
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Zheng,Yu,Yang,Hong-Dou,Wei,Kun,et al. Synthetic Studies toward Parvistemoline Using Asymmetric Ir/Amine-Catalyzed Allylation[J]. JOURNAL OF ORGANIC CHEMISTRY,2021,86(8):6025-6029.
APA Zheng,Yu,Yang,Hong-Dou,Wei,Kun,&Yang,Yu-Rong.(2021).Synthetic Studies toward Parvistemoline Using Asymmetric Ir/Amine-Catalyzed Allylation.JOURNAL OF ORGANIC CHEMISTRY,86(8),6025-6029.
MLA Zheng,Yu,et al."Synthetic Studies toward Parvistemoline Using Asymmetric Ir/Amine-Catalyzed Allylation".JOURNAL OF ORGANIC CHEMISTRY 86.8(2021):6025-6029.
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