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Asymmetric Synthesis and Crystal Structure of a Bioactive Morpholine Derivative 被引量:2

Asymmetric Synthesis and Crystal Structure of a Bioactive Morpholine Derivative
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摘要 A novel morpholine derivative was synthesized by Michael addition/internal nucleophilic substitution of 4-(L)-menthyloxy(1R,2S,5R)-butenolide with phenyl-glyalcohol under mild condition, and its structure was determined by X-ray diffraction. The target compound belongs to orthorhombic, space group P212121 with a = 5.7729(7), b = 11.5032(14), c = 25.161(3)A, Mr = 319.35, Z = 4, V = 1670.8(4)A^3, Dc = 1.270 g/cm3, μ(MoKα) = 0.094 mm^-1, F(000) = 680, Flack = 0.01(2), R = 0.0398 and wR = 0.0914. A novel morpholine derivative was synthesized by Michael addition/internal nucleophilic substitution of 4-(L)-menthyloxy(1R,2S,5R)-butenolide with phenyl-glyalcohol under mild condition, and its structure was determined by X-ray diffraction. The target compound belongs to orthorhombic, space group P212121 with a = 5.7729(7), b = 11.5032(14), c = 25.161(3)A, Mr = 319.35, Z = 4, V = 1670.8(4)A^3, Dc = 1.270 g/cm3, μ(MoKα) = 0.094 mm^-1, F(000) = 680, Flack = 0.01(2), R = 0.0398 and wR = 0.0914.
出处 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2007年第5期515-518,共4页 结构化学(英文)
基金 Financially supported by the National Natural Science Foundation of China (No. 29672004)
关键词 morpholine derivative α-phenyl-glyalcohol 4-(L)-menthyloxy-butenolide asymmetric synthesis morpholine derivative, α-phenyl-glyalcohol,4-(L)-menthyloxy-butenolide, asymmetric synthesis
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