Preparation and NMR Study of 7,7′-(α,ω-Alkanediyl)bis[theophylline], 1,1′-(α,ω-Alkanediyl)bis[theobromine], and 1,1′-(α,ω-Alkanediyl)bis[3-methyluracil]-Reference-Cited by-同舟云学术

Preparation and NMR Study of 7,7′-(α,ω-Alkanediyl)bis[theophylline], 1,1′-(α,ω-Alkanediyl)bis[theobromine], and 1,1′-(α,ω-Alkanediyl)bis[3-methyluracil]

Published:1994-01 Issue:1 Volume:67 Page:203-209
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Itahara Toshio,Imamura Kazuhiko

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj/67/1/67_1_203/_pdf

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1. Synthetic spectroscopic models related to coenzymes and base pairs. II. Evidence for intramolecular base-base interactions in dinucleotide analogs

2. Synthetic spectroscopic models related to coenzymes and base pairs. III. A 1,1'-trimethylene-linked thymine photodimer of cis-syn structure

3. Synthetic spectroscopic models related to coenzymes and base pairs. XI. Solid state ultraviolet irradiation of 1,1'-trimethylenebisthymine and photosensitized irradiation of 1,1'-polymethylenebisthymines

4. Crystal and molecular structure of 1,1'-trimethylenebisthymine (Thy-C3-Thy). Environment of a solid state photochemical reaction

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