A new SmI2-mediated coupling reaction between N-acyl lactams and ketones or aldehydes is reported. The ring opening of these imides with samarium diiodide gives acyl samarium species, which are trapped by ketones or aldehydes to yield amido alpha-ketols. With an excess of SmI2, in the presence of ethanol, the end products are amidoketones. (C) 2000 Elsevier Science Ltd. All rights reserved.
机构:
Kobe Gakuin Univ, Fac Pharmaceut Sci, Nishi Ku, Kobe, Hyogo 6512180, JapanKobe Gakuin Univ, Fac Pharmaceut Sci, Nishi Ku, Kobe, Hyogo 6512180, Japan
Yoshimura, K
Nakata, D
论文数: 0引用数: 0
h-index: 0
机构:
Kobe Gakuin Univ, Fac Pharmaceut Sci, Nishi Ku, Kobe, Hyogo 6512180, JapanKobe Gakuin Univ, Fac Pharmaceut Sci, Nishi Ku, Kobe, Hyogo 6512180, Japan
Nakata, D
Hioki, K
论文数: 0引用数: 0
h-index: 0
机构:
Kobe Gakuin Univ, Fac Pharmaceut Sci, Nishi Ku, Kobe, Hyogo 6512180, JapanKobe Gakuin Univ, Fac Pharmaceut Sci, Nishi Ku, Kobe, Hyogo 6512180, Japan
Hioki, K
Tani, S
论文数: 0引用数: 0
h-index: 0
机构:
Kobe Gakuin Univ, Fac Pharmaceut Sci, Nishi Ku, Kobe, Hyogo 6512180, JapanKobe Gakuin Univ, Fac Pharmaceut Sci, Nishi Ku, Kobe, Hyogo 6512180, Japan