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• W2100077498 abstract "An efficient enantioselective cascade sulfa-Michael/Michael addition reaction of trans-3-(2-mercaptophenyl)-2-propenoic acid ethyl ester with nitroalkenes catalyzed by a chiral squaramide catalyst was disclosed. This cascade reaction afforded thiochroman derivatives with three contiguous stereocenters in high yields (up to 94%), excellent diastereoselectivities (up to >25:1 dr) and enantioselectivities (up to 99% ee)." @default.
• W2100077498 created "2016-06-24" @default.
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• W2100077498 date "2014-08-25" @default.
• W2100077498 modified "2023-09-24" @default.
• W2100077498 title "Enantioselective Construction of Functionalized Thiochromans via Squaramide-Catalyzed Asymmetric Cascade Sulfa-Michael/Michael Addition" @default.
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• W2100077498 doi "https://doi.org/10.1002/cjoc.201400391" @default.
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