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- W2740183266 abstract "The substituted tetrahydrofuran moiety can be found in a number of natural products possessing interesting biological properties. Quite a few reports describe 2,5-cis-diastereoselective [3+2] cycloadditions of 2-substituted cyclopropane-1,1-diesters with aldehydes. In this work, trans-2,3-disubstituted cyclopropane-1,1-diesters are considered as substrates. While common 2,5-cis-products were obtained with electron-neutral and -poor aromatic aldehydes, electron-rich analogues furnished 2,5-trans-adducts with excellent diastereoselectivities." @default.
- W2740183266 created "2017-08-08" @default.
- W2740183266 date "2011-03-18" @default.
- W2740183266 modified "2023-09-26" @default.
- W2740183266 title "Highly Regio- and Diastereoselective [3+2] Cycloadditions" @default.
- W2740183266 doi "https://doi.org/10.1055/s-0030-1259670" @default.
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