机译:对(-)-Kinamycin F和(-)-Lomaiviticin糖苷配基的对映选择性合成路线的发展。
Department of Chemistry, Yale University, New Haven, Connecticut 06520, United States;
Department of Chemistry, Yale University, New Haven, Connecticut 06520, United States;
Department of Chemistry, Yale University, New Haven, Connecticut 06520, United States;
Department of Chemistry, Yale University, New Haven, Connecticut 06520, United States;
Department of Chemistry, Yale University, New Haven, Connecticut 06520, United States;
Department of Chemistry, Yale University, New Haven, Connecticut 06520, United States;
Department of Chemistry, Yale University, New Haven, Connecticut 06520, United States;
机译:(-)-Kinamycin F和(-)-Lomaiviticin Aglycon的对映选择性合成
机译:(-)-Lomaiviticin糖苷配子的11步对映选择性合成
机译:Lomaiviticin糖苷配基全碳骨架的对映选择性合成在二聚化过程中显示了显着的远程取代基效应
机译:对糖尿病髓内的Friedel-Crafts与醇的反应:取代四氢咔唑的创新合成途径
机译:开发一种简单的,对映选择性的合成盐孢菌酰胺A类似物的合成路线。
机译:不对称合成路线发展以( - ) - Kinamycin F和( - ) - Lomaiviticin苷元
机译:研究lomaiviticin和kinamycin的全合成,锁定核酸的新进入,高活性的可修饰Rh(II)催化剂的开发和直接醇胺化合成羟胺