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Nickel-catalyzed hydrocarboxylation of ynamides with CO2 and H2O : observation of unexpected regioselectivity

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Please use this identifier to cite or link to this item:http://hdl.handle.net/2115/70974

Title: Nickel-catalyzed hydrocarboxylation of ynamides with CO2 and H2O : observation of unexpected regioselectivity
Authors: Doi, Ryohei Browse this author
Abdullah, Iman Browse this author
Taniguchi, Takahisa Browse this author
Saito, Nozomi Browse this author
Sato, Yoshihiro Browse this author →KAKEN DB
Issue Date: 14-Jul-2017
Publisher: Royal Society of Chemistry
Journal Title: Chemical communications
Volume: 53
Issue: 55
Start Page: 7720
End Page: 7723
Publisher DOI: 10.1039/c7cc03127k
PMID: 28569298
Abstract: We describe the nickel-catalyzed hydrocarboxylation of ynamides with CO2 and H2O to afford a variety of alpha-amino-alpha, beta-unsaturated esters with high regioselectivities. The selective alpha-carboxylation of ynamides with this catalytic protocol is unexpected in view of the electronic bias of ynamides and is in sharp contrast to our previous study in which a stoichiometric amount of Ni(0) was used to form a beta-carboxylated product exclusively. We revealed that this unexpected C-C bond formation was induced by the combination of Zn and MgBr2.
Type: article (author version)
URI: http://hdl.handle.net/2115/70974
Appears in Collections:薬学研究院 (Faculty of Pharmaceutical Sciences) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 土井 良平

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