A diastereo-and enantioselective Michael addition of chiral amide enolates to α, β-unsaturated esters a stereoelective synthesis of (+)-dehydroiridodiol and (−)- …
M Yamaguchi, K Hasebe, S Tanaka, T Minami
Index: Yamaguchi, Masahiko; Hasebe, Koichi; Tanaka, Shinya; Minami, Toru Tetrahedron Letters, 1986 , vol. 27, # 8 p. 959 - 962
Full Text: HTML
Citation Number: 58
Abstract
Download full text in PDF Opens in a new window. Article suggestions will be shown in a dialog on return to ScienceDirect. ... Please enable JavaScript to use all the features on this page. ... (+)-Dehydroiridodiol and (−)-isodehydroiridodiol were synthesized stereoselectively using the diastereo- and enantioselective Michael addition of chiral amide enolates to α, β-unsaturated esters. ... J. Org. Chem., 48 (1983), p. 5364 However, we found it more convenient to ...
Related Articles:
A study on the influence of a silicon group on the Curtius reaction
[Verma, Rekha; Ghosh, Sunil K. Journal of the Chemical Society - Perkin Transactions 1, 1998 , # 15 p. 2377 - 2381]
[Oehme, G.; Pracejus, H. Journal fuer Praktische Chemie (Leipzig), 1980 , vol. 322, # 5 p. 798 - 808]