ChemInform Abstract: Palladium-Catalyzed Three-Component Reaction of N-Tosyl Hydrazones, Isonitriles and Amines Leading to Amidines.

ChemInform ◽  
2016 ◽  
Vol 47 (12) ◽  
pp. no-no
Author(s):  
Qiang Dai ◽  
Yan Jiang ◽  
Jin-Tao Yu ◽  
Jiang Cheng
Keyword(s):  
Three Component Reaction ◽  
Palladium Catalyzed

Palladium‐Catalyzed Three‐Component Reaction of Allenes, Aryl Iodides, and Diazo Compounds: Approach to 1,3‐Dienes

2013 ◽  
Vol 125 (35) ◽  
pp. 9475-9478 ◽  
Author(s):  
Qing Xiao ◽  
Binglong Wang ◽  
Leiming Tian ◽  
Yang Yang ◽  
Jian Ma ◽  
...  
Keyword(s):  
Diazo Compounds ◽  
Aryl Iodides ◽  
Three Component Reaction ◽  
Palladium Catalyzed

A palladium-catalyzed three-component reaction for the preparation of quinazolin-4(3H)-imines

2012 ◽  
Vol 48 (23) ◽  
pp. 2903 ◽  
Author(s):  
Guanyinsheng Qiu ◽  
Gang Liu ◽  
Shouzhi Pu ◽  
Jie Wu
Keyword(s):  
Three Component Reaction ◽  
Palladium Catalyzed

Palladium-catalyzed three-component reaction of N-tosyl hydrazones, isonitriles and amines leading to amidines

2015 ◽  
Vol 51 (93) ◽  
pp. 16645-16647 ◽  
Author(s):  
Qiang Dai ◽  
Yan Jiang ◽  
Jin-Tao Yu ◽  
Jiang Cheng
Keyword(s):  
Three Component Reaction ◽  
Palladium Catalyzed

A palladium-catalyzed three-component reaction between N-tosyl hydrazones, aryl isonitriles and amines was developed, leading to amidines in moderate to good yields.

Regio- and Stereoselective Palladium-Catalyzed Intermolecular Three-Component Aryletherification of Terminal Allenes

Synthesis ◽  
2018 ◽  
Vol 50 (20) ◽  
pp. 4097-4103 ◽  
Author(s):  
Shufeng Chen ◽  
Xin-Xing Wu ◽  
Chenjun Wang ◽  
Wanrong Zhao ◽  
Haiying Zhao
Keyword(s):  
Steric Effect ◽  
High Selectivity ◽  
Aryl Iodides ◽  
Three Component Reaction ◽  
Palladium Catalyzed ◽  
One Step

A palladium-catalyzed three-component intermolecular aryl­etherification reaction of ferrocene-substituted allenes, aryl iodides and phenols or alcohols is reported. In this three-component reaction, two new C–C and C–O bonds are formed in one step with high regio- and stereoselectivity. The high selectivity obtained in this reaction can be attributed to the steric effect of the bulky ferrocene group.

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