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-3H-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.
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