114155-71-4Relevant academic research and scientific papers
Stereoselective and Site-Specific Allylic Alkylation of Amino Acids and Small Peptides via a Pd/Cu Dual Catalysis
Huo, Xiaohong,He, Rui,Fu, Jingke,Zhang, Jiacheng,Yang, Guoqiang,Zhang, Wanbin
supporting information, p. 9819 - 9822 (2017/08/02)
We report a stereoselective and site-specific allylic alkylation of Schiff base activated amino acids and small peptides via a Pd/Cu dual catalysis. A range of noncoded α,α-dialkyl α-amino acids were easily synthesized in high yields and with excellent enantioselectivities (up to >99% ee). Furthermore, a direct and highly stereoselective synthesis of small peptides with enantiopure α-alkyl or α,α-dialkyl α-amino acids residues incorporated at specific sites was accomplished using this dual catalyst system.
Conformationally constrained renin inhibitory peptides: γ-lactam-bridged dipeptide isostere as conformational restriction
Thaisrivongs,Pals,Turner,Kroll
, p. 1369 - 1376 (2007/10/02)
A model of the conformation of the enzyme-bound inhibitor of human renin suggested the possibility of a γ-lactam conformational restriction at the P2-P3 site. Synthetic routes to these γ-lactam dipeptide isosteres and their incorpora
