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:
Kyushu Univ, Inst Fundamental Res Organ Chem, Higashi Ku, Fukuoka 8128581, JapanKyushu Univ, Inst Fundamental Res Organ Chem, Higashi Ku, Fukuoka 8128581, Japan
Kikukawa, T
Hanamoto, T
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Kyushu Univ, Inst Fundamental Res Organ Chem, Higashi Ku, Fukuoka 8128581, JapanKyushu Univ, Inst Fundamental Res Organ Chem, Higashi Ku, Fukuoka 8128581, Japan
Hanamoto, T
Inanaga, J
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Kyushu Univ, Inst Fundamental Res Organ Chem, Higashi Ku, Fukuoka 8128581, JapanKyushu Univ, Inst Fundamental Res Organ Chem, Higashi Ku, Fukuoka 8128581, Japan
机构:
Kyushu Univ, Inst Fundamental Res Organ Chem, Higashi Ku, Fukuoka 8128581, JapanKyushu Univ, Inst Fundamental Res Organ Chem, Higashi Ku, Fukuoka 8128581, Japan
Kikukawa, T
Hanamoto, T
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h-index: 0
机构:
Kyushu Univ, Inst Fundamental Res Organ Chem, Higashi Ku, Fukuoka 8128581, JapanKyushu Univ, Inst Fundamental Res Organ Chem, Higashi Ku, Fukuoka 8128581, Japan
Hanamoto, T
Inanaga, J
论文数: 0引用数: 0
h-index: 0
机构:
Kyushu Univ, Inst Fundamental Res Organ Chem, Higashi Ku, Fukuoka 8128581, JapanKyushu Univ, Inst Fundamental Res Organ Chem, Higashi Ku, Fukuoka 8128581, Japan