机译:N-烷基化聚对苯甲酰胺的螺旋结构
Contribution from the Synthesis and Control,PRESTO,Japan Science and Technology Agency (JST),Japan,Department of Applied Chemistry,Kanagawa University,Rokkakubashi,Kanagawa-ku,Yokohama 221-8686,Japan,Faculty of Pharmaceutical Sciences at Kagawa Campu;
Contribution from the Synthesis and Control,PRESTO,Japan Science and Technology Agency (JST),Japan,Department of Applied Chemistry,Kanagawa University,Rokkakubashi,Kanagawa-ku,Yokohama 221-8686,Japan,Faculty of Pharmaceutical Sciences at Kagawa Campu;
Contribution from the Synthesis and Control,PRESTO,Japan Science and Technology Agency (JST),Japan,Department of Applied Chemistry,Kanagawa University,Rokkakubashi,Kanagawa-ku,Yokohama 221-8686,Japan,Faculty of Pharmaceutical Sciences at Kagawa Campu;
Contribution from the Synthesis and Control,PRESTO,Japan Science and Technology Agency (JST),Japan,Department of Applied Chemistry,Kanagawa University,Rokkakubashi,Kanagawa-ku,Yokohama 221-8686,Japan,Faculty of Pharmaceutical Sciences at Kagawa Campu;
Contribution from the Synthesis and Control,PRESTO,Japan Science and Technology Agency (JST),Japan,Department of Applied Chemistry,Kanagawa University,Rokkakubashi,Kanagawa-ku,Yokohama 221-8686,Japan,Faculty of Pharmaceutical Sciences at Kagawa Campu;
Contribution from the Synthesis and Control,PRESTO,Japan Science and Technology Agency (JST),Japan,Department of Applied Chemistry,Kanagawa University,Rokkakubashi,Kanagawa-ku,Yokohama 221-8686,Japan,Faculty of Pharmaceutical Sciences at Kagawa Campu;
Contribution from the Synthesis and Control,PRESTO,Japan Science and Technology Agency (JST),Japan,Department of Applied Chemistry,Kanagawa University,Rokkakubashi,Kanagawa-ku,Yokohama 221-8686,Japan,Faculty of Pharmaceutical Sciences at Kagawa Campu;
Contribution from the Synthesis and Control,PRESTO,Japan Science and Technology Agency (JST),Japan,Department of Applied Chemistry,Kanagawa University,Rokkakubashi,Kanagawa-ku,Yokohama 221-8686,Japan,Faculty of Pharmaceutical Sciences at Kagawa Campu;
Contribution from the Synthesis and Control,PRESTO,Japan Science and Technology Agency (JST),Japan,Department of Applied Chemistry,Kanagawa University,Rokkakubashi,Kanagawa-ku,Yokohama 221-8686,Japan,Faculty of Pharmaceutical Sciences at Kagawa Campu;
Contribution from the Synthesis and Control,PRESTO,Japan Science and Technology Agency (JST),Japan,Department of Applied Chemistry,Kanagawa University,Rokkakubashi,Kanagawa-ku,Yokohama 221-8686,Japan,Faculty of Pharmaceutical Sciences at Kagawa Campu;
机译:N-烷基化聚对苯甲酰胺梳状聚合物中烷基侧链的堆积方式和构象转变
机译:聚(对-苯甲酰胺)和聚[2-亚苯基(5-苯并咪唑)]的溶致嵌段共聚物:三元体系共聚物聚(对-苯甲酰胺)二甲基乙酰胺氯化锂
机译:具有异丙基取代的手性三(乙二醇)侧链的聚(对苯甲酰胺):合成和螺旋构象
机译:基于平面轴向螺旋手足式继电器的多米诺效应诱导单手螺旋寡核苷酸(p-苯甲酰胺)S.
机译:官能化间位聚亚苯基乙炔基螺旋结构的建模与合成。
机译:通过在聚甲基丙烯酸甲酯螺旋腔中富勒烯结合的螺旋肽的包封形成螺旋中的螺旋超结构
机译:N-烷基化聚(P-苯甲酰胺)的螺旋结构
机译:聚(1,5-萘 - 苯并二恶唑)和聚(2,6-萘 - 苯并二恶唑)的晶体结构,分子模拟和形态