Palladium-catalyzed tandem cyclization/suzuki coupling reaction of 1, 2,7-trienes
Zhu GG(朱钢国) ; Zhang ZG(张兆国)
刊名Org. Lett.
2004
卷号6期号:22页码:4041-4044
ISSN号1523-7060
其他题名钯催化的1,2,7-三烯的环化-Suzuki偶联反应
通讯作者张兆国
英文摘要A Pd(0)-catalyzed 1,2,7-triene cyclization/arylation cascade reaction was realized via pi-allylpalladium intermediate formation and a subsequent Suzuki coupling reaction to preferentially give a five-membered ring product with a stereodefined exocyclic double bond. Excellent cis/trans selectivity was achieved (only cis-3 was isolated) with heteroatom-tethered 1,2,7-triene substrates.
学科主题金属有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1021/ol048301r
语种英语
WOS记录号WOS:000224691900041
公开日期2013-08-14
内容类型期刊论文
源URL[http://202.127.28.38/handle/331003/27607]  
专题上海有机化学研究所_上海有机化学研究所
推荐引用方式
GB/T 7714
Zhu GG,Zhang ZG. Palladium-catalyzed tandem cyclization/suzuki coupling reaction of 1, 2,7-trienes[J]. Org. Lett.,2004,6(22):4041-4044.
APA 朱钢国,&张兆国.(2004).Palladium-catalyzed tandem cyclization/suzuki coupling reaction of 1, 2,7-trienes.Org. Lett.,6(22),4041-4044.
MLA 朱钢国,et al."Palladium-catalyzed tandem cyclization/suzuki coupling reaction of 1, 2,7-trienes".Org. Lett. 6.22(2004):4041-4044.
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