Auto-tandem Catalysis of Triflic Imide in Organic Synthesis

被引:0
|
作者
Takasu, Kiyosei [1 ]
机构
[1] Kyoto Univ, Grad Sch Pharmaceut Sci, Sakyo Ku, Kyoto 6068501, Japan
关键词
auto-tandem catalysis; triflic imide; silyl triflic imide; domino reaction; rapid synthesis; divergent synthesis; cycloadditions; isomerization; elimination; hydride transfer; electrocyclization; SILYL ENOL ETHERS; DIELS-ALDER REACTION; CYCLOBUTANE RING FORMATION; BOND-FORMING REACTIONS; FUNCTIONALIZED CYCLOBUTANES; TETRASUBSTITUTED FURANS; FACILE ISOMERIZATION; 3+2 CYCLOADDITION; CASCADE REACTION; PAESSLERIN-A;
D O I
10.5059/yukigoseikyokaishi.72.770
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Domino reactions have received great attention as efficient synthetic methodologies to construct structurally complex molecules from simple materials in a single operation. Recently a new concept, "tandem catalysis" in domino reactions has been proposed. Tandem catalysis is categorized into three subclasses: Orthogonal, auto-, and assisted-tandem catalysis. Auto-tandem catalysis is defined as a process in which one catalyst promotes more than two mechanistically different reactions in a single vessel. It has been discovered by several researchers including us that triflic imide (Tf2NH) activates a variety of chemical transformations, such as Mukaiyama-aldol reaction, conjugate addition, cycloadditions and so on. This account summarizes our recent development of auto-tandem catalysis of triflic imide.
引用
收藏
页码:770 / 780
页数:11
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