Nucleophilic Catalysis of Amide Isomerization

1999 ◽  
Vol 121 (34) ◽  
pp. 7963-7964 ◽  
Author(s):  
Christopher Cox ◽  
Harald Wack ◽  
Thomas Lectka
RNA ◽  
2007 ◽  
Vol 13 (7) ◽  
pp. 967-973 ◽  
Author(s):  
H. Walbott ◽  
C. Husson ◽  
S. Auxilien ◽  
B. Golinelli-Pimpaneau

ChemInform ◽  
2010 ◽  
Vol 22 (2) ◽  
pp. no-no
Author(s):  
I. N. ROZHKOV ◽  
S. M. IGUMNOV ◽  
S. I. PLETNEV ◽  
I. V. CHAPLINA

Tetrahedron ◽  
1989 ◽  
Vol 45 (7) ◽  
pp. 1959-1974 ◽  
Author(s):  
Robert J.P. Corriu ◽  
Gérard F. Lanneau ◽  
Dominique Leclercq

2020 ◽  
pp. 174751982092575
Author(s):  
Meng Yao ◽  
Xia Chen ◽  
Yuling Lu ◽  
Zhenhua Guan ◽  
Zengwei Luo ◽  
...  

An efficient method for N-acylation of amides is described using a pyridine ring as the internal nucleophilic catalyst to give imides in moderate to excellent yields. The methodology provides a facile, air insensitive, and environmentally friendly route to form diversified imide scaffolds, which exist widely in natural products and biologically active materials.


1979 ◽  
Vol 101 (20) ◽  
pp. 6020-6022 ◽  
Author(s):  
Michael A. Hierl ◽  
Edward P. Gamson ◽  
Irving M. Klotz

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