Palladium-Catalyzed Intramolecular α-Arylation of α-Amino Acid Esters

2002 ◽  
Vol 67 (2) ◽  
pp. 465-475 ◽  
Author(s):  
Oliver Gaertzen ◽  
Stephen L. Buchwald
2012 ◽  
Vol 8 ◽  
pp. 2004-2018 ◽  
Author(s):  
Rajendra Surasani ◽  
Dipak Kalita ◽  
A V Dhanunjaya Rao ◽  
K B Chandrasekhar

Simple and efficient procedures for palladium-catalyzed cross-coupling reactions of N-substituted 4-bromo-7-azaindole (1H-pyrrole[2,3-b]pyridine), with amides, amines, amino acid esters and phenols through C–N and C–O bond formation have been developed. The C–N cross-coupling reaction of amides, amines and amino acid esters takes place rapidly by using the combination of Xantphos, Cs2CO3, dioxane and palladium catalyst precursors Pd(OAc)2/Pd2(dba)3. The combination of Pd(OAc)2, Xantphos, K2CO3 and dioxane was found to be crucial for the C–O cross-coupling reaction. This is the first report on coupling of amides, amino acid esters and phenols with N-protected 4-bromo-7-azaindole derivatives.


2019 ◽  
Vol 55 (27) ◽  
pp. 3947-3950 ◽  
Author(s):  
Wenhui Wang ◽  
Hanmin Huang

A new and efficient reaction has been developed to synthesize α-alkoxy-β-amino acid esters via palladium-catalyzed formal insertion of carbenoids into N,O-aminals.


2017 ◽  
Vol 129 (50) ◽  
pp. 16142-16146 ◽  
Author(s):  
Lu Ouyang ◽  
Jianxiao Li ◽  
Jia Zheng ◽  
Jiuzhong Huang ◽  
Chaorong Qi ◽  
...  

ChemInform ◽  
2010 ◽  
Vol 33 (26) ◽  
pp. no-no
Author(s):  
Oliver Gaertzen ◽  
Stephen L. Buchwald

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