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• W2010537036 abstract "A series of cis-2,3-disubstituted cyclopropane 1,1-diesters were examined in the AlCl3-promoted [3 + 2]-annulations with aldehydes. In this reaction, these cis-cyclopropanes displayed reactivities starkly different from their trans counterparts in terms of the high chemical yields (up to 98%) and provided the desired annulation products with excellent diastereomeric purity. This protocol provides a facile and highly stereoselective way to construct synthetically useful pentasubstituted tetrahydrofurans not easily accessible using other methods." @default.
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• W2010537036 date "2013-05-09" @default.
• W2010537036 modified "2023-09-23" @default.
• W2010537036 title "<i>cis</i>-2,3-Disubstituted Cyclopropane 1,1-Diesters in [3 + 2] Annulations with Aldehydes: Highly Diastereoselective Construction of Densely Substituted Tetrahydrofurans" @default.
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• W2010537036 doi "https://doi.org/10.1021/jo400554a" @default.
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