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Enantioselective one-pot synthesis of 4H-chromene derivatives catalyzed by a chiral Ni(ii) complex.


ABSTRACT: A Ni(ii)-bis(oxazoline) complex and p-TSOH are used to form enantioenriched 4H-chromenes from ortho-quinone methides (o-QMs) and dicarbonyls, providing the desired products in up to 95% ee. The method is compatible with various β-ketoester substrates, and the products obtained could be converted into biologically active 4H-chromene derivatives.

SUBMITTER: Yu X 

PROVIDER: S-EPMC9058437 | biostudies-literature | 2020 Dec

REPOSITORIES: biostudies-literature

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Enantioselective one-pot synthesis of 4<i>H</i>-chromene derivatives catalyzed by a chiral Ni(ii) complex.

Yu Xuan X   Lan Wenjie W   Li Jiaqi J   Bai Hui H   Qin Zhaohai Z   Fu Bin B  

RSC advances 20201216 72


A Ni(ii)-bis(oxazoline) complex and <i>p</i>-TSOH are used to form enantioenriched 4<i>H</i>-chromenes from <i>ortho</i>-quinone methides (<i>o</i>-QMs) and dicarbonyls, providing the desired products in up to 95% ee. The method is compatible with various β-ketoester substrates, and the products obtained could be converted into biologically active 4<i>H</i>-chromene derivatives. ...[more]

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