Fluorescence quenching of Y-4,9-dihydro-4,6-dimethyl-9-oxo-1H-imidazo-1,2-a purine (Yt base) and the model compounds Yt(CH2)nadenine by α-bromonaphthalene-Reference-Cited by-同舟云学术

Fluorescence quenching of Y-4,9-dihydro-4,6-dimethyl-9-oxo-1H-imidazo-1,2-a purine (Yt base) and the model compounds Yt(CH2)nadenine by α-bromonaphthalene

Published:1982-01 Issue:1 Volume:20 Page:71-76
ISSN:0047-2670
Container-title:Journal of Photochemistry
language:en
Short-container-title:Journal of Photochemistry

Author:

Gryczyński I.,Kawski A.,Paszyc S.,Skalski B.

Publisher

Elsevier BV

Subject

General Physics and Astronomy,General Chemical Engineering,General Chemistry

Reference16 articles.

1. THEORETICAL ANALYSIS OF THE PHOTOPHYSICAL PROPERTIES OF ε-ADENINE AND THE RNApheY-BASE

2. Study of the phosphorescent bases of yeast phenylalanine transfer RNA with the aid of optical detection of magnetic resonance

3. Effect of the Removal of the Y Base on the Conformation of Yeast tRNAPhe

4. Photochemical properties of Ytbase in aqueous solution

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1. Theoretical evaluation of nonclassical nucleic acid bases. 3. Structures and properties of Wye tautomers;The Journal of Physical Chemistry;1993-11

2. Electronic linear dichroism spectrum and transition moment directions of the hypermodified nucleic acid base Wye;The Journal of Physical Chemistry;1990-05

3. Decay time distribution analysis of Yt-base in benzene—methanol mixtures;Journal of Photochemistry and Photobiology B: Biology;1989-11

4. Acrylmide quenching of Yt-base fluorescence in aqueous solution;Biophysical Chemistry;1988-09

5. The modified components of transfer ribonucleic acids.;Journal of Synthetic Organic Chemistry, Japan;1987