Tandem Gold(III)‐Catalyzed Amination‐Intramolecular Hydroamination Reactions of 1‐En‐4‐yn‐3‐ols with Sulfonamides: Efficient Approach to Highly Substituted Pyrroles | Zendy

Shu XingZhong | Zendy; Liu XueYuan | Zendy; Xiao HuiQuan | Zendy; Ji KeGong | Zendy; Guo LiNa | Zendy; Liang YongMin | Zendy

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Tandem Gold(III)‐Catalyzed Amination‐Intramolecular Hydroamination Reactions of 1‐En‐4‐yn‐3‐ols with Sulfonamides: Efficient Approach to Highly Substituted Pyrroles

Author(s) -

Shu XingZhong,

Liu XueYuan,

Xiao HuiQuan,

Ji KeGong,

Guo LiNa,

Liang YongMin

Publication year - 2008

Publication title -

advanced synthesis and catalysis

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 1.541

H-Index - 155

eISSN - 1615-4169

pISSN - 1615-4150

DOI - 10.1002/adsc.200700452

Subject(s) - hydroamination , amination , chemistry , intramolecular force , tandem , catalysis , combinatorial chemistry , organic chemistry , materials science , composite material

A simple, convenient and efficient synthetic approach to highly substituted pyrroles has been developed by utilizing a gold(III)‐catalyzed tandem amination‐intramolecular hydroamination reaction. The first examples of gold‐catalyzed, selective amination of 1‐en‐4‐yn‐3‐ols have also been disclosed.

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