Enantioselective Fluorescent Recognition of Amino Acids by Amide Formation: An Unusual Concentration Effect

2017 ◽  
Vol 82 (23) ◽  
pp. 12669-12673 ◽  
Author(s):  
Chao Wang ◽  
Chaoyuan Zeng ◽  
Xiaoling Zhang ◽  
Lin Pu
1998 ◽  
Vol 39 (23) ◽  
pp. 4103-4106 ◽  
Author(s):  
H.M. Meshram ◽  
Gondi Sudershan Reddy ◽  
M. Muralidhar Reddy ◽  
J.S. Yadav

Synthesis ◽  
1989 ◽  
Vol 1989 (01) ◽  
pp. 37-39 ◽  
Author(s):  
Shui-Tein Chen ◽  
Shih-Hsiung Wu ◽  
Kung-Tsung Wang

2019 ◽  
Vol 25 (33) ◽  
pp. 7773-7773
Author(s):  
Yuan‐Yuan Zhu ◽  
Xue‐Dan Wu ◽  
Mehdi Abed ◽  
Shuang‐Xi Gu ◽  
Lin Pu

2008 ◽  
Vol 61 (2) ◽  
pp. 131 ◽  
Author(s):  
Andrew B. Hughes ◽  
Brad E. Sleebs

Results from studies of the Arndt–Eistert homologation of N-methyl-α-amino acids with concomitant ester and amide formation is discussed. The applicability of the use of ultrasound was investigated in the Wolff rearrangement of diazoketones for the production of esters and amides. This methodology was then applied to a novel ‘N-methyl coupling’ that allows simultaneous β-amino acid formation. Conventional ‘PyBroP N-methyl couplings’ were also performed as a comparison to establish the validity of the method.


2020 ◽  
Vol 26 (32) ◽  
pp. 7258-7262 ◽  
Author(s):  
Feng Zhao ◽  
Yalin Wang ◽  
Xuedan Wu ◽  
Shanshan Yu ◽  
Xiaoqi Yu ◽  
...  

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