Chiral alcohol-induced diastereoselective conjugate addition and cyclization
C Fang, H Suemune, K Sakai
Index: Fang, Chenglin; Suemune, Hiroshi; Sakai, Kiyoshi Tetrahedron Letters, 1990 , vol. 31, # 33 p. 4751 - 4754
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Citation Number: 20
Abstract
All compounds obtained in this manner gave satisfactory spectroscopic data. Selected spectroscopic data for representative products are as follows. 11a (n=1, RPh): IR (neat): 3450, 1725, 1600, 1180 cm −1 . 1 HNMR (CDCl 3 ) δ: 2.85 (1H, m, CHCO), 3.18 (1H, m, CHPh), 3.30 (1H, m, HCO), 4.41 (1H, m, CHOCO), 7.24 (5H, m, aromatic-H). MS (m/z): 288 (M + ), 190, 144, 118. [α]D 26 −148.3° (c=0.12, CHCl 3 ). 11b (n=1, RPh): IR (neat): 3450, 1725, ...
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