TY - JOUR
T1 - Asymmetric total synthesis of MK8383
T2 - the iron-mediated coupling reaction is the only effective method for the construction of the (Z)-trisubstituted side-chain alkene
AU - Hayashi, Nobuyuki
AU - Nakada, Masahisa
N1 - Funding Information:
We thank Dr. Nobuto Minowa (Meiji Seika Kaishya, Ltd, Japan) for kindly providing a sample of MK8383. This work was financially supported in part by a Waseda University Grant for Special Research Projects, a Grant-in-Aid for Scientific Research (B), and the Global COE program ‘Center for Practical Chemical Wisdom’ by MEXT.
PY - 2009/1/14
Y1 - 2009/1/14
N2 - The first asymmetric total synthesis of MK8383 through the iron-mediated coupling reaction is described. In this total synthesis, the key step was clearly the stereoselective construction of the (Z)-trisubstituted side-chain alkene. Although this problem was seemingly easy to resolve, in fact it presented us an opportunity to evaluate the coupling reactions reported to date, and the iron-mediated coupling reaction was found to be the only effective method for the stereoselective construction of the (Z)-trisubstituted side-chain alkene.
AB - The first asymmetric total synthesis of MK8383 through the iron-mediated coupling reaction is described. In this total synthesis, the key step was clearly the stereoselective construction of the (Z)-trisubstituted side-chain alkene. Although this problem was seemingly easy to resolve, in fact it presented us an opportunity to evaluate the coupling reactions reported to date, and the iron-mediated coupling reaction was found to be the only effective method for the stereoselective construction of the (Z)-trisubstituted side-chain alkene.
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U2 - 10.1016/j.tetlet.2008.10.138
DO - 10.1016/j.tetlet.2008.10.138
M3 - Article
AN - SCOPUS:56949103894
SN - 0040-4039
VL - 50
SP - 232
EP - 235
JO - Tetrahedron Letters
JF - Tetrahedron Letters
IS - 2
ER -