Pd-Catalyzed oxidative isomerization of propargylic acetates: highly efficient access to α-acetoxyenones via alkenyl Csp2–O bond-forming reductive elimination from PdIV

2016 ◽  
Vol 52 (70) ◽  
pp. 10644-10647 ◽  
Author(s):  
Jun Li ◽  
Wenjie Yang ◽  
Fachao Yan ◽  
Qing Liu ◽  
Ping Wang ◽  
...  

A Pd(ii)/(iv)-catalyzed oxidative isomerization of propargylic acetates developed for the synthesis of polysubstituted alkenyl acetates is described.

2020 ◽  
Vol 56 (85) ◽  
pp. 13052-13052
Author(s):  
Jun Li ◽  
Wenjie Yang ◽  
Fachao Yan ◽  
Qing Liu ◽  
Ping Wang ◽  
...  

Correction for ‘Pd-Catalyzed oxidative isomerization of propargylic acetates: highly efficient access to α-acetoxyenones via alkenyl Csp2–O bond-forming reductive elimination from PdIV’ by Jun Li et al., Chem. Commun., 2016, 52, 10644–10647, DOI: 10.1039/C6CC04463H.


Author(s):  
Ruixia Liu ◽  
Jingkuo Han ◽  
Bin Li ◽  
Xian Liu ◽  
Zhao Wei ◽  
...  

A highly efficient intramolecular asymmetric reductive amination transformation catalyzed by an iridium complex of tBu-ax-Josiphos has been realized, providing an efficient access to various THIQ alkaloids.


Tetrahedron ◽  
2019 ◽  
Vol 75 (2) ◽  
pp. 137-143 ◽  
Author(s):  
Quan Jiang ◽  
D. Matthew Peacock ◽  
John F. Hartwig ◽  
Thomas R. Cundari

2017 ◽  
Vol 53 (56) ◽  
pp. 7961-7964 ◽  
Author(s):  
Jie Wang ◽  
Ruoyu Sang ◽  
Xiaolong Chong ◽  
Yinuo Zhao ◽  
Wenjie Fan ◽  
...  

A copper-catalyzed C(sp3)–H bond functionalization of simple alkanes with olefinic amides was developed for the synthesis of benzoxazine derivatives.


ChemInform ◽  
2005 ◽  
Vol 36 (46) ◽  
Author(s):  
Sylvain Antoniotti ◽  
Emilie Genin ◽  
Veronique Michelet ◽  
Jean-Pierre Genet

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