A Theoretical Rationale why Furan-side Monoadduct is More Favorable Toward Diadduct Formation in 8-Methoxypsoralen and Thymine Complexes-Reference-Cited by-同舟云学术

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A Theoretical Rationale why Furan-side Monoadduct is More Favorable Toward Diadduct Formation in 8-Methoxypsoralen and Thymine Complexes

Published:2013-04-04 Issue:4 Volume:89 Page:891-899
ISSN:0031-8655
Container-title:Photochemistry and Photobiology
language:en
Short-container-title:Photochem Photobiol

Author:

Huang Xuebin¹,Zhang Rubo¹

Affiliation:

1. Key Laboratory of Cluster Science; School of Chemistry; Beijing Institute of Technology; Beijing; China

Publisher

Wiley

Subject

Physical and Theoretical Chemistry,General Medicine,Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/php.12067/fullpdf

Reference38 articles.

1. Phototherapy and Photochemotherapy of Skin Diseases

2. Photoreaction of new psoralen analogs with DNA: Sequence and mutation specificity in the Escherichia coli lacZ gene;Collet;Photochem. Photobiol.,1997

3. Quantum chemical study on the population of the lowest triplet state of psoralen;Serrano-Pérez;Chem. Phys. Lett.,2007

4. Photosensitization and phototherapy with furocoumarins: A quantum chemical study;Serrano-Pérez;Chem. Phys.,2008

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