Potassiumtert-Butoxide-Mediated Amine Acyl Exchange Reaction ofN,N-Disubstituted Formamides with Aromatic Carbonyl DerivativesviaSequential CN Bond Cleavage/Formation: an Approach to Aromatic Amides

2015 ◽  
Vol 357 (13) ◽  
pp. 2855-2861 ◽  
Author(s):  
Ming-Zhong Zhang ◽  
Qing-Hu Guo ◽  
Wen-Bing Sheng ◽  
Can-Cheng Guo
ChemCatChem ◽  
2013 ◽  
Vol 5 (5) ◽  
pp. 1101-1115 ◽  
Author(s):  
Masafumi Hirano ◽  
Ryo Fujimoto ◽  
Kohei Hatagami ◽  
Nobuyuki Komine ◽  
Sanshiro Komiya

ACS Catalysis ◽  
2021 ◽  
pp. 8678-8683
Author(s):  
Runyou Ye ◽  
Maoshuai Zhu ◽  
Xufei Yan ◽  
Yang Long ◽  
Ying Xia ◽  
...  

2005 ◽  
Author(s):  
◽  
Endre Szuromi

Tetranuclear Pt(II) oxo-complex [(COD)4Pt4([mu]3-O)2Cl2](BF4)2 (1) (COD = 1,5- cyclooctadiene) was found to readily react with a variety of alkenes (ethylene, norbornene, propylene and cyclopentene). The most significant discovery resulted from the norbornene reaction, which gave platinaoxetane [(COD)2Pt2(OC7H10)Cl]BF4 (4), the first metallaoxetane obtained from the direct reaction of an oxo complex and an alkene. A facile alkene-exchange reaction was observed between platinaoxetane 4 and norbornene-derivative 5 giving a new platinaoxetane and free norbornene. Kinetic studies revealed that the reaction is catalyzed by possibly more than one electrophilic catalyst.We describe two probable mechanisms for the reaction.Cationic Pt(II) complexes (COD)Pt(OTf)2 and [(COD)Pt(THF)(OTf)]OTf were found to readily react with alkenes such as norbornenes, cyclopentene, propylene and ethylene.Two common features of these reactions were alkene C-H bond cleavage and triflic acid elimination. Norbornenes, cyclopentene and ethylene gave alkene-coupled products, while propylene resulted in a simple allyl complex.


1972 ◽  
Vol 94 (4) ◽  
pp. 1410-1411 ◽  
Author(s):  
S. Karady ◽  
S. H. Pines ◽  
L. M. Weinstock ◽  
F. E. Roberts ◽  
G. S. Brenner ◽  
...  

2016 ◽  
Vol 14 (16) ◽  
pp. 3869-3872 ◽  
Author(s):  
Yongjun Bian ◽  
Xingyu Qu

A new acyl–acyl exchange reaction has been developed for the formation of aryl esters from primary aryl amides. The reaction could occur under mild reaction conditions with catalytic quantities of K2CO3, and could afford moderate to good yields of the desired products.


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