Synthesis and Photochemical Behavior of Peptide Nucleic Acid Dimers and Analogues Containing 4-Thiothymine: Unprecedented (5−4) Photoadduct Reversion-Reference-Cited by-同舟云学术

Synthesis and Photochemical Behavior of Peptide Nucleic Acid Dimers and Analogues Containing 4-Thiothymine: Unprecedented (5−4) Photoadduct Reversion

Published:1998-02-01 Issue:6 Volume:120 Page:1157-1166
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Clivio Pascale¹,Guillaume Dominique¹,Adeline Marie-Thérèse¹,Hamon Jeanine¹,Riche Claude¹,Fourrey Jean-Louis¹

Affiliation:

1. Contribution from the Institut de Chimie des Substances Naturelles, CNRS, 91198 Gif-sur-Yvette Cedex, France, and the Laboratoire de Chimie Thérapeutique, Faculté de Pharmacie, Université René Descartes, 4 Avenue de l'Observatoire, 75006 Paris, France

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja971983b

Reference68 articles.

1. Sequence-Selective Recognition of DNA by Strand Displacement with a Thymine-Substituted Polyamide

2. Biochemical Evidence That a D-Loop Is Part of a Four-Stranded PNA−DNA Bundle. Nickel-Mediated Cleavage of Duplex DNA by a Gly-Gly-His Bis-PNA

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