Chiral Pharmaceutical Intermediaries Obtained by Reduction of 2-Halo-1-(4-substituted phenyl)-ethanones Mediated by Geotrichum candidum CCT 1205 and Rhodotorula glutinis CCT 2182
摘要:
(300 MHz, CDCl3) δ 2.74 (sl, 1H, OH), 3.48 (dd, 1H, J = 7.0 Hz and 11.3 Hz, CH2), 3.61 (dd, 1H, J = 5.8 Hz and 11.3 Hz, CH2), 4.87 (dd, 1H, J = 5.8 Hz and 7.0 Hz, CH), 7.24-7.28 (m, 2H, Ph), 7.31-7.51 (m, 2H, Ph); 13C NMR (75 MHz, CDCl3) δ 39.72, 72.97, 122.12, 127.43, 131.56, 139.00; MS m/z (rel. int. %): 143 (29), 142 (11), 141 (100), 139 (4), 138 (2), 121 (7), 115 (6), 113 (16), 112 (6), 111 (4), 108 (7), 107 (5), 105 (4), 104 (2), 103 (2), 102 (2), 91 (2), 89 (1), 79 (11), 78 (9), 77 (70), 76 (2), 75 (15), 74 (9), 70 (6), 63 (8), 51 (28), 50 (30), 49 (3), 44 (22), 43 (20), 40 (32).
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