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- W2020170648 abstract "While the first reaction step provides a mixture of four diastereomers, the second step completes the access to 6,6- and 6,7-fused carbocyclic skeletons with three new rings and four new stereocenters with moderate to excellent diastereoselectivities." @default.
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- W2020170648 date "2015-03-01" @default.
- W2020170648 modified "2023-09-25" @default.
- W2020170648 title "ChemInform Abstract: Tandem Diels-Alder [4 + 2] Cycloadditions and Intramolecular [3 + 2] Cross-Cycloadditions of Dienylcyclopropane 1,1-Diesters." @default.
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- W2020170648 doi "https://doi.org/10.1002/chin.201512141" @default.
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