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Synthesis of Ferrocene Oxazoline N,O ligands and Their Application in Asymmetric Ethyl- and Phenylzinc Additions to Aldehydes

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NIAID Data Ecosystem2026-03-09 收录
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https://figshare.com/articles/dataset/Synthesis_of_Ferrocene_Oxazoline_N_O_ligands_and_Their_Application_in_Asymmetric_Ethyl_and_Phenylzinc_Additions_to_Aldehydes/2120839
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The synthesis of a range of novel gem-disubstituted ferrocene–oxazoline ligands and their application in both the asymmetric ethyl- and phenylzinc additions to aldehydes is reported. These studies reveal that gem-disubstitution of i-Pr-containing ferrocene oxazoline ligands results in increased enantioselectivity compared to their unsubstituted counterparts. Utilizing zinc catalysis, these ligands provided a wide range of secondary alcohols in yields of up to 93% with ee’s of up to >99%. An interesting crystal structure of a ferrocene oxide–lithium tetramer showing lithium–nitrogen coordination in the solid state is also presented.
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2016-02-12
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