Total synthesis of (−)-epimyrtine by a gold-catalyzed hydroamination approach
…, KH Nguyen, P de Aguiar Amaral…
Index: Trinh, Thi Thanh Huyen; Nguyen, Khanh Hung; De Aguiar Amaral, Patricia; Gouault, Nicolas Beilstein Journal of Organic Chemistry, 2013 , vol. 9, p. 2042 - 2047
Full Text: HTML
Citation Number: 17
Abstract
Abstract A new approach to the total synthesis of (−)-epimyrtine has been developed from D- alanine. The key step to access the enantiopure pyridone intermediate was achieved by a gold-mediated cyclization. Finally, various transformations afforded the natural product in a few steps and good overall yield.
Related Articles:
TAPP analogs containing β3??homo??amino acids: synthesis and receptor binding
[Podwysocka; Kosson; Lipkowski; Olma, Aleksandra Journal of Peptide Science, 2012 , vol. 18, # 9 p. 556 - 559]