Kinetic studies of intramolecular hydrogen bonding in methyl and ethyl salicylates and salicylaldehyde by ultrasonic absorption measurement

1969 ◽  
Vol 73 (3) ◽  
pp. 477-482 ◽  
Author(s):  
Tatsuya Yasunaga ◽  
Nobuhide Tatsumoto ◽  
Hiroshi Inoue ◽  
Masaji Miura
Synlett ◽  
2019 ◽  
Vol 30 (08) ◽  
pp. 928-931 ◽  
Author(s):  
Ruiting Yuan ◽  
Qinghui Shou ◽  
Qaiser Mahmood ◽  
Guangqiang Xu ◽  
Xitong Sun ◽  
...  

The kinetics of the ring-opening polymerization of ε-caprolactone with butane-1,4-diol as the initiator and 1,5,7-triazabicyclo[4.4.0]dec-5-ene as catalyst were examined. A highly efficient and controllable polymerization of ε-caprolactone occurred with an activation energy of 22.5 kJ·mol–1, which is much lower than that observed with butan-1-ol as the initiator (39.5 kJ·mol–1). An intramolecular hydrogen-bonding-assisted mechanism is proposed to explain this lowering of the activation energy.


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.


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