scholarly journals Taming the Reactivity of Alkyl Azides by Intramolecular Hydrogen Bonding: Site-Selective Conjugation of Unhindered Diazides

Author(s):  
Koshiro Maegawa ◽  
Hiroki Tanimoto ◽  
Seiji Onishi ◽  
Takenori Tomohiro ◽  
Tsumoru Morimoto ◽  
...  

Organic azides are still in the center of click chemistry connecting two molecules. However, taming the conjugation selectivity of azides is difficult without the help of the bulky groups. We...

2019 ◽  
Vol 10 (11) ◽  
pp. 3324-3329 ◽  
Author(s):  
Jan-Philipp Berndt ◽  
Yevhenii Radchenko ◽  
Jonathan Becker ◽  
Christian Logemann ◽  
Dhaka R. Bhandari ◽  
...  

Site-selective nitrenoid insertions are made possible with a postfunctionalized dirhodium(ii)-catalyst equipped with a remote hydrogen bonding site.


2008 ◽  
Vol 112 (51) ◽  
pp. 16782-16787 ◽  
Author(s):  
Kyung-Koo Lee ◽  
Eunmyung Kim ◽  
Cheonik Joo ◽  
Jaewook Song ◽  
Hogyu Han ◽  
...  

2009 ◽  
Vol 113 (11) ◽  
pp. 3590-3590
Author(s):  
Kyung-Koo Lee ◽  
Eunmyung Kim ◽  
Cheonik Joo ◽  
Jaewook Song ◽  
Hogyu Han ◽  
...  

2012 ◽  
Vol 2012 ◽  
pp. 1-10 ◽  
Author(s):  
Shiao-Wei Kuo ◽  
Jing-Long Hong ◽  
Yu-Chan Huang ◽  
Jem-Kun Chen ◽  
Shih-Kang Fan ◽  
...  

New star poly(N-isopropylacrylamide)-b-polyhedral oligomeric silsesquioxane (PNIPAm-b-POSS) copolymers were synthesized from octa-azido functionalized POSS (N3-POSS) and alkyne-PNIPAm, which was prepared using an alkyne-functionalized atom transfer radical polymerization (ATRP) initiator (propargyl 2-bromo-2-methylpropionamide), via click chemistry. These star PNIPAm-b-POSS copolymers undergo a sharp coil-globule transition in water at above 32°C changing from a hydrophilic state below this temperature to a hydrophobic state above it, which is similar to linear PNIPAm homopolymers. More interestingly, we found that these star polymers exhibited strong blue photoluminescence in water above a lower critical solution temperature (LCST). This photoluminescence was likely due to the constrained geometric freedom and relatively rigid structure caused by intramolecular hydrogen bonding within the star PNIPAm polymers, which exhibit an intrinsic fluorescent behavior.


10.1002/jcc.2 ◽  
1996 ◽  
Vol 17 (16) ◽  
pp. 1804-1819 ◽  
Author(s):  
Attila Kov�cs ◽  
Istv�n Kolossv�ry ◽  
G�bor I. Csonka ◽  
Istv�n Hargittai

2019 ◽  
Vol 58 (14) ◽  
pp. 9443-9451 ◽  
Author(s):  
Song Xu ◽  
Hyuk-Yong Kwon ◽  
Daniel C. Ashley ◽  
Chun-Hsing Chen ◽  
Elena Jakubikova ◽  
...  

2012 ◽  
Vol 2012 (24) ◽  
pp. 4483-4492 ◽  
Author(s):  
Ronald K. Castellano ◽  
Yan Li ◽  
Edwin A. Homan ◽  
Andrew J. Lampkins ◽  
Iris V. Marín ◽  
...  

Molecules ◽  
2021 ◽  
Vol 26 (12) ◽  
pp. 3763
Author(s):  
Poul Erik Hansen

This review outlines methods to investigate the structure of natural products with emphasis on intramolecular hydrogen bonding, tautomerism and ionic structures using NMR techniques. The focus is on 1H chemical shifts, isotope effects on chemical shifts and diffusion ordered spectroscopy. In addition, density functional theory calculations are performed to support NMR results. The review demonstrates how hydrogen bonding may lead to specific structures and how chemical equilibria, as well as tautomeric equilibria and ionic structures, can be detected. All these features are important for biological activity and a prerequisite for correct docking experiments and future use as drugs.


Sign in / Sign up

Export Citation Format

Share Document