Anthranilic acid-containing cyclic tetrapeptides: at the crossroads of conformational rigidity and synthetic accessibility
Abstract
Easier to prepare than cyclic tri- and tetra-peptides, more rigid than 13-membered rings containing other β-amino acids, and adopts stereochemically-tunable homogenous conformations.
Document Details
- Document Type
- Pub Defense Publication
- Publication Date
- Jan 01, 2016
- Source ID
- 10.1039/c6ob00693k
Entities
People
- Dongyue Xin
- Kevin Burgess
Organizations
- Cancer Prevention and Research Institute of Texas
- National Institutes of Health
- Texas A&M University
- United States Army
- United States Department of Defense
- Yusuf Hamied Department of Chemistry