Palladium catalyzed direct allylation of azlactones with simple allylic alcohols in the absence of any activators

RSC Advances ◽  
2014 ◽  
Vol 4 (49) ◽  
pp. 25596-25599 ◽  
Author(s):  
Hui Zhou ◽  
Huameng Yang ◽  
Hongyu Yin ◽  
Muwen Liu ◽  
Chungu Xia ◽  
...  

The first example of the readily scalable direct allylic alkylation of azlactones with simple allylic alcohols has been developed, which is catalyzed by Pd(PPh3)4 alone in the absence of any activators under neutral conditions.

2014 ◽  
Vol 126 (26) ◽  
pp. 6894-6898 ◽  
Author(s):  
Xiaohong Huo ◽  
Guoqiang Yang ◽  
Delong Liu ◽  
Yangang Liu ◽  
Ilya D. Gridnev ◽  
...  

2017 ◽  
Vol 6 (5) ◽  
pp. 520-526 ◽  
Author(s):  
Yongseok Kwon ◽  
Jaehyun Jung ◽  
Jae Hyun Kim ◽  
Woo-Jung Kim ◽  
Sanghee Kim

ChemInform ◽  
2015 ◽  
Vol 46 (1) ◽  
Author(s):  
Xiaohong Huo ◽  
Guoqiang Yang ◽  
Delong Liu ◽  
Yangang Liu ◽  
Ilya D. Gridnev ◽  
...  

2014 ◽  
Vol 53 (26) ◽  
pp. 6776-6780 ◽  
Author(s):  
Xiaohong Huo ◽  
Guoqiang Yang ◽  
Delong Liu ◽  
Yangang Liu ◽  
Ilya D. Gridnev ◽  
...  

1996 ◽  
Vol 25 (12) ◽  
pp. 1021-1022 ◽  
Author(s):  
Yuzuki Tada ◽  
Akiharu Satake ◽  
Isao Shimizu ◽  
Akio Yamamoto

Author(s):  
Tiantian Chen ◽  
Yang Yang ◽  
Liyu Xie ◽  
Haijian Yang ◽  
Guangbin Dong ◽  
...  

<p>We report a Ni(0)-catalyzed cross coupling reaction between simple ketones and 1,3-dienes. A variety of a-allylic alkylation products were formed in an 1,2-addition manner with excellent regioselectivity. Water was found to significantly accelerate this transformation. A HO-Ni-H species generated from oxidative addition of Ni(0) to H<sub>2</sub>O is proposed to play a “dual role” in activating both the ketone and the diene substrate.</p>


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