Copyright © 2014 John Wiley & Sons, Ltd. A series of pyridoxine derivatives was investigated by 1H and 2D nuclear overhauser enhancement spectroscopy (NOESY) NMR. The free energies of activation for the pyridyl-oxygen rotation of the 2,4-dinitrophenyl ether of the seven-membered acetals of pyridoxine were measured by dynamic NMR. A conformational exchange between the chair and twist forms of the seven-membered acetal ring was confirmed by dynamic NMR and STO3G computations
Copyright © 2016 John Wiley & Sons, Ltd.The conformational properties of three pyridoxine derivative...
© 2015 John Wiley & Sons, Ltd. Two pyridoxine derivatives containing a dinitrophenyl moiety were inv...
© 2015 John Wiley & Sons, Ltd. Two pyridoxine derivatives containing a dinitrophenyl moiety were inv...
Copyright © 2014 John Wiley & Sons, Ltd. A series of pyridoxine derivatives was investigated by 1H a...
Copyright © 2014 John Wiley & Sons, Ltd. A series of pyridoxine derivatives was investigated by 1H a...
A series of pyridoxine derivatives was investigated by 1H and 2D nuclear overhauser enhancement spec...
A series of pyridoxine derivatives was investigated by 1H and 2D nuclear overhauser enhancement spec...
A series of pyridoxine derivatives was investigated by 1H and 2D nuclear overhauser enhancement spec...
A series of pyridoxine derivatives was investigated by 1H and 2D nuclear overhauser enhancement spec...
© 2016 John Wiley & Sons, Ltd.The conformational properties of three pyridoxine derivatives were stu...
© 2016 John Wiley & Sons, Ltd.The conformational properties of three pyridoxine derivatives were stu...
© 2016 John Wiley & Sons, Ltd.The conformational properties of three pyridoxine derivatives were stu...
Copyright © 2016 John Wiley & Sons, Ltd.The conformational properties of three pyridoxine derivative...
© 2016 John Wiley & Sons, Ltd.The conformational properties of three pyridoxine derivatives were stu...
Copyright © 2016 John Wiley & Sons, Ltd.The conformational properties of three pyridoxine derivative...
Copyright © 2016 John Wiley & Sons, Ltd.The conformational properties of three pyridoxine derivative...
© 2015 John Wiley & Sons, Ltd. Two pyridoxine derivatives containing a dinitrophenyl moiety were inv...
© 2015 John Wiley & Sons, Ltd. Two pyridoxine derivatives containing a dinitrophenyl moiety were inv...
Copyright © 2014 John Wiley & Sons, Ltd. A series of pyridoxine derivatives was investigated by 1H a...
Copyright © 2014 John Wiley & Sons, Ltd. A series of pyridoxine derivatives was investigated by 1H a...
A series of pyridoxine derivatives was investigated by 1H and 2D nuclear overhauser enhancement spec...
A series of pyridoxine derivatives was investigated by 1H and 2D nuclear overhauser enhancement spec...
A series of pyridoxine derivatives was investigated by 1H and 2D nuclear overhauser enhancement spec...
A series of pyridoxine derivatives was investigated by 1H and 2D nuclear overhauser enhancement spec...
© 2016 John Wiley & Sons, Ltd.The conformational properties of three pyridoxine derivatives were stu...
© 2016 John Wiley & Sons, Ltd.The conformational properties of three pyridoxine derivatives were stu...
© 2016 John Wiley & Sons, Ltd.The conformational properties of three pyridoxine derivatives were stu...
Copyright © 2016 John Wiley & Sons, Ltd.The conformational properties of three pyridoxine derivative...
© 2016 John Wiley & Sons, Ltd.The conformational properties of three pyridoxine derivatives were stu...
Copyright © 2016 John Wiley & Sons, Ltd.The conformational properties of three pyridoxine derivative...
Copyright © 2016 John Wiley & Sons, Ltd.The conformational properties of three pyridoxine derivative...
© 2015 John Wiley & Sons, Ltd. Two pyridoxine derivatives containing a dinitrophenyl moiety were inv...
© 2015 John Wiley & Sons, Ltd. Two pyridoxine derivatives containing a dinitrophenyl moiety were inv...