Bioinspired Synthesis of Chiral 3,4-Dihydropyranones via S-to-O Acyl-Transfer Reactions

2018 ◽  
Vol 20 (6) ◽  
pp. 1584-1588 ◽  
Author(s):  
Hui Jin ◽  
Juyeol Lee ◽  
Hu Shi ◽  
Jin Yong Lee ◽  
Eun Jeong Yoo ◽  
...  
1975 ◽  
Vol 75 (5) ◽  
pp. 627-649 ◽  
Author(s):  
Andrew Williams ◽  
K. T. Douglas

1970 ◽  
Vol 48 (2) ◽  
pp. 218-220
Author(s):  
W. J. D. Whish ◽  
T. Viswanatha

The ability of α-N-acetylcycloserine to participate in acyl transfer reactions has been investigated. The reaction with cinnamoylimidazole yields a stable monocinnamoyl intermediate, while that with p-nitrophenyl acetate yields a derivative which undergoes facile deacylation. The kinetics of acylation of α-N-acetylcycloserine and of the deacylation of its acetyl intermediate are reported.


Sign in / Sign up

Export Citation Format

Share Document