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• W4248004265 abstract "Unfortunately, an error in the Schemes was propagated through all the stages of the publication, the result being that the isoxazolidines are drawn as the enantiomers of the actual established structures. The correct structures are provided below. Table of Contents: 1 Table 1: 1 Table 2: 1 Table 3: 1 Scheme 1: Scheme 3: Corrections for the Experimental Section appear as follows: (3R,4R)-4-methyl-2-N-3-diphenyl-isoxazoline-4-carbaldehyde (6a) instead of (3S,4S)-4-methyl-2-N-3-diphenyl-isoxazoline-4-carbaldehyde (6a) (3R,4S)-4-methyl-2-N-3-diphenyl-isoxazoline-4-methanol (8a) instead of (3S,4S)-4-methyl-2-N-3-diphenyl-isoxazoline-4-methanol (8a) (3R,4R)-4-methyl-3-(4-nitro-phenyl)-isoxazoline-4-carbaldehyde (6b) instead of (3S,4S)-4-methyl-3-(4-nitro-phenyl)-isoxazoline-4-carbaldehyde (6b) (3R,4S)-4-methyl-3-(4-nitro-phenyl)-2-phenyl-isoxazoline-4-methanol (8b) instead of (3S,4S)-4-methyl-3-(4-nitro-phenyl)-2-phenyl-isoxazoline-4-methanol (8b) (3R,4R)-4-methyl-3-(4-trifluoromethyl-phenyl)-isoxazoline-4-carbaldehyde (6c) instead of (3S,4S)-4-methyl-3-(4-trifluoromethyl-phenyl)-isoxazoline-4-carbaldehyde (6c) (3R,4S)-4-methyl-3-(4-trifluoromethyl-phenyl)-2-phenyl-isoxazoline-4-methanol (8c) instead of (3S,4S)-4-methyl-3-(4-trifluoromethyl-phenyl)-2-phenyl-isoxazoline-4-methanol (8c) (3R,4R)-4-methyl-3-(4-chloro-phenyl)-isoxazoline-4-carbaldehyde (6d) instead of (3S,4S)-4-methyl-3-(4-chloro-phenyl)-isoxazoline-4-carbaldehyde (6d) (3R,4S)-4-methyl-3-(4-chloro-phenyl)-2-phenyl-isoxazoline-4-methanol (8d) instead of (3S,4S)-4-methyl-3-(4-chloro-phenyl)-2-phenyl-isoxazoline-4-methanol (8d) (3R,4R)-4-methyl-3-(4-methyl-phenyl)-isoxazoline-4-carbaldehyde (6e) instead of (3S,4S)-4-methyl-3-(4-methyl-phenyl)-isoxazoline-4-carbaldehyde (6e) (3R,4S)-4-methyl-3-(4-methyl-phenyl)-2-phenyl-isoxazoline-4-methanol (8e) instead of (3S,4S)-4-methyl-3-(4-methyl-phenyl)-2-phenyl-isoxazoline-4-methanol (8e) (3R,4R)-4-methyl-3-(4-methoxy-phenyl)-isoxazoline-4-carbaldehyde (6f) instead of (3S,4S)-4-methyl-3-(4-methoxy-phenyl)-isoxazoline-4-carbaldehyde (6f) (3R,4S)-4-methyl-3-(4-methoxy-phenyl)-2-phenyl-isoxazoline-4-methanol (8f) instead of (3S,4S)-4-methyl-3-(4-methoxy-phenyl)-2-phenyl-isoxazoline-4-methanol (8f) (3R,4R)-4-methyl-3-(4-cyano-phenyl)-isoxazoline-4-carbaldehyde (6g) instead of (3S,4S)-4-methyl-3-(4-cyano-phenyl)-isoxazoline-4-carbaldehyde (6g) (3R,4S)-4-methyl-3-(4-cyano-phenyl)-2-phenyl-isoxazoline-4-methanol (8g) instead of (3S,4S)-4-methyl-3-(4-cyano-phenyl)-2-phenyl-isoxazoline-4-methanol (8g) (3R,4R)-4-methyl-3-(2-naphthyl)-isoxazoline-4-carbaldehyde (6h) instead of (3S,4S)-4-methyl-3-(2-naphthyl)-isoxazoline-4-carbaldehyde (6h) (3R,4S)-4-methyl-3-(2-naphthyl)-2-phenyl-isoxazoline-4-methanol (8h) instead of (3S,4S)-4-methyl-3-(2-naphthyl)-2-phenyl-isoxazoline-4-methanol (8h) (3R,4R)-4-methyl-3-(2-furyl)-isoxazoline-4-carbaldehyde (6i) instead of (3S,4S)-4-methyl-3-(2-furyl)-isoxazoline-4-carbaldehyde (6i) (3R,4S)-4-methyl-3-(2-furyl)-2-phenyl-isoxazoline-4-methanol (8i) instead of (3S,4S)-4-methyl-3-(2-furyl)-2-phenyl-isoxazoline-4-methanol (8i) (3R,4R)-4-methyl-3-phenyl-2-(4-methoxy-phenyl)-isoxazoline-4-carbaldehyde (6j) instead of (3S,4S)-4-methyl-3-phenyl-2-(4-methoxy-phenyl)-isoxazoline-4-carbaldehyde (6j) (3R,4S)-4-methyl-3-phenyl-2-(4-methoxy-phenyl)-isoxazoline-4-methanol (8j) instead of (3S,4S)-4-methyl-3-phenyl-2-(4-methoxy-phenyl)-isoxazoline-4-methanol (8j) (2S,4S)-2-methyl-4-phenyl-4-(phenylamino)butane-1,2-diol (13a) and (R)-2-methyl-2-(phenyl(phenylamino)methyl)propane-1,3-diol (14a) instead of (2R,4R)-2-methyl-4-phenyl-4-(phenylamino)butane-1,2-diol (13a) and (S)-2-methyl-2-(phenyl(phenylamino)methyl)propane-1,3-diol (14a)" @default.
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• W4248004265 date "2009-07-06" @default.
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• W4248004265 title "Iron- and Ruthenium-Lewis Acid Catalyzed Asymmetric 1,3-Dipolar Cycloaddition Reactions between Enals and Diaryl Nitrones" @default.
• W4248004265 doi "https://doi.org/10.1002/asia.200990022" @default.
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