| Literature DB >> 32372645 |
Yinhua Huang1, Liangyao Xu1, Feifei Yu1, Wenzhou Shen1, Xiunan Lu1, Liyuan Ding1, Liangjun Zhong2, Guofu Zhong1, Jian Zhang1.
Abstract
A practical and atom-economic protocol for the stereoselective preparation of various 1,4- and 1,3-diene skeletons through iridium-catalyzed directed olefinic C-H allylation and alkenylation of NH-Ts acrylamides in water was developed. This reaction tolerated a wide scope of substrates under simple reaction conditions and enabled successful gram-scale preparation. Furthermore, an asymmetric variant of this reaction giving enantioenriched 1,4-dienes was achieved employing a chiral diene-iridium complex as the catalyst.Entities:
Year: 2020 PMID: 32372645 DOI: 10.1021/acs.joc.0c00619
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354