Amino acid esters of 9-(2?,3?-dihydroxypropyl-1?)-adenine are the specific inhibitors of protein synthesis on ribosomes

1973 ◽  
Vol 1 (3) ◽  
pp. 173-178 ◽  
Author(s):  
B. P. Gottikh ◽  
A. A. Krayevsky ◽  
M. K. Kukhanova ◽  
A. A. Jatsyna ◽  
A. M. Kritzyn ◽  
...  



Synfacts ◽  
2006 ◽  
Vol 2006 (12) ◽  
pp. 1253-1253
Author(s):  
Y. Hamada ◽  
K. Makino ◽  
M. Iwasaki


2021 ◽  
Vol 294 ◽  
pp. 198290
Author(s):  
Lidia A. Baltina ◽  
Mann-Jen Hour ◽  
Ya-Chi Liu ◽  
Young-Sheng Chang ◽  
Su-Hua Huang ◽  
...  






Synlett ◽  
2020 ◽  
Author(s):  
Xiaohua Liu ◽  
Yi Li ◽  
Hao Pan ◽  
Wang-Yuren Li ◽  
Xiaoming Feng

AbstractAn asymmetric organocatalytic nucleophilic aromatic substitution reaction of azlactones with electron-deficient aryls was established. A variety of α-aryl α-alkyl α-amino acid esters and peptides were obtained in decent yields and stereoselectivities. A new bifunctional catalytic mode involving charge-transfer interaction and hydrogen bonding is proposed to explain the enantioselectivity.



1977 ◽  
Vol 8 (50) ◽  
pp. no-no
Author(s):  
YU. A. DAVIDOVICH ◽  
V. I. BUTAEVA ◽  
O. M. GALKIN ◽  
T. N. SENTSOVA ◽  
S. V. ROGOZHIN






Sign in / Sign up

Export Citation Format

Share Document