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Asymmetric Synthesis and Crystal Structure of a Bioactive Morpholine Derivative
Authors:WANG Jian-Ping  FU Yong-Ju  WANG Jian-Ge  QIN Jian-Hua  CHEN Qing-Hua
Abstract: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.
Keywords:morpholine derivative  α-phenyl-glyalcohol  4-(L)-menthyloxy-butenolide  asymmetric synthesis  Derivative  Morpholine  Crystal Structure  Synthesis  space  group  target  compound  structure  diffraction  butenolide  mild  condition  internal  nucleophilic substitution  novel  morpholine  derivative  synthesized  Michael addition
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