1072115-75-3Relevant academic research and scientific papers
C-I···π Halogen Bonding Driven Supramolecular Helix of Bilateral N-Amidothioureas Bearing β-Turns
Cao, Jinlian,Yan, Xiaosheng,He, Wenbin,Li, Xiaorui,Li, Zhao,Mo, Yirong,Liu, Maili,Jiang, Yun-Bao
supporting information, p. 6605 - 6610 (2017/06/05)
We report the first example of C-I···π halogen bonding driven supramolecular helix in highly dilute solution of micromolar concentration, using alanine based bilateral I-substituted N-amidothioureas that contain helical fragments, the β-turn structures. T
Synthesis of some 2,2′:6′,2″-terpyridines disubstituted in positions 6 and 6″ with head-to-tail oriented amino acids and dipeptides: A simple entry to a reversible inducer of folding in amino acid sequences
Annunziata, Rita,Benaglia, Maurizio,Puglisi, Alessandra,Raimondi, Laura,Cozzi, Franco
supporting information; experimental part, p. 3976 - 3983 (2009/04/10)
The 2,2′:6′,2″-terpyridine scaffold has been identified as a conformationally discrete structural element potentially capable of inducing reversible folding in substituents, attached through suitable spacers to its 6,6″-positions, by metal complexation/de
