机译:一种新颖有效的合成取代烯烃的方法; NaHSO_4 / SiO_2对两种不同的醇进行交叉偶联
Department of Materials and Applied Chemistry, College of Science and Technology, Ninon University, Kanda Surugadai, Chiyoda-ku, Tokyo, Japan;
Department of Materials and Applied Chemistry, College of Science and Technology, Ninon University, Kanda Surugadai, Chiyoda-ku, Tokyo, Japan;
Department of Materials and Applied Chemistry, College of Science and Technology, Ninon University, Kanda Surugadai, Chiyoda-ku, Tokyo, Japan;
Department of Materials and Applied Chemistry, College of Science and Technology, Ninon University, Kanda Surugadai, Chiyoda-ku, Tokyo, Japan;
Department of Materials and Applied Chemistry, College of Science and Technology, Ninon University, Kanda Surugadai, Chiyoda-ku, Tokyo, Japan;
The Institute of Natural Sciences, College of Humanities and Science, Nihon University, Japan;
机译:在NaHSO_4 / SiO_2存在下,在醇和α-硝基酮的3-酰基异恶唑啉的简单有效的单壶合成
机译:NaNO_2 / NaHSO_4·H_2O / SiO_2在温和条件下氧化芳基取代的氨基脲的简单有效方法
机译:NaNO_2 / NaHSO_4·H_2O / SiO_2合成α,β-不饱和酰基偶氮化合物的有效方法
机译:通过PD催化的交叉联轴器合成5-取代 - 尿嘧啶PNA单体
机译:I:Buchwald-Hartwig-Yagupol'skii胺化反应,以及使用Pd-PEPPSI-IPr合成二取代和三取代的烯烃II:Negishi烷基-烷基交叉偶联方案的机械解释,使用NMR光谱学
机译:取代的烯烃和亚胺的区域和立体选择性交叉偶联。聚合的立体选择性合成饱和的15-氨基醇和取代的哌啶
机译:取代的烯烃和亚胺的测定和立体选择性交叉偶联。饱和1,5-氨基醇和取代哌啶的收敛立体选择性合成