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- W2895875830 endingPage "1186" @default.
- W2895875830 startingPage "1182" @default.
- W2895875830 abstract "Abstract A well‐designed three‐component reaction was developed to construct a class of optically active carbazolespirooxindole‐urazoles in good yields with excellent stereoselectivities via tandem Diels‐Alder reaction and ene‐reaction. The driving force originating from aromatization with in situ generated carbazolespirooxindole and the high reactivity of 4‐phenyl‐3 H ‐1,2,4‐triazole‐3,5‐dione facilitate the ene‐reaction in mild conditions. Control experiments indicated that the excellent stereoselectivities of ene‐reaction most likely came from the spatial configuration of the carbazolespirooxindole. The obtained products could be converted to other synthetic useful structures via diverse functionalization." @default.
- W2895875830 created "2018-10-26" @default.
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- W2895875830 date "2018-10-17" @default.
- W2895875830 modified "2023-10-16" @default.
- W2895875830 title "Stereoselective Construction of Complex Spirooxindoles via Bisthiourea Catalyzed Three-Component Reactions" @default.
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- W2895875830 doi "https://doi.org/10.1002/cjoc.201800368" @default.
- W2895875830 hasPublicationYear "2018" @default.
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