Catalytic enantioselective domino oxa-michael/aldol condensations: asymmetric synthesis of benzopyran derivatives |
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Authors: | Sundén Henrik Ibrahem Ismail Zhao Gui-Ling Eriksson Lars Córdova Armando |
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Affiliation: | Department of Organic Chemistry, The Arrhenius Laboratory, Stockholm University, 10691 Stockholm, Sweden. |
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Abstract: | The first direct organocatalytic asymmetric domino oxa-Michael/aldol condensation reaction is presented. The unprecedentedly simple, chiral, pyrrolidine-catalyzed asymmetric domino reactions between salicylic aldehyde derivatives and alpha,beta-unsaturated aldehydes proceed with high chemo- and enantioselectivities to give the corresponding chromene-3-carbaldehyde derivatives in high yields and with ee values of 83-98%. |
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Keywords: | asymmetric catalysis diphenylprolinol domino reactions heterocycles oxa‐Michael reaction |
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