Spiropyran Photoswitches in the Context of DNA: Synthesis and Photochromic Properties
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Title
Spiropyran Photoswitches in the Context of DNA: Synthesis and Photochromic Properties
Authors
Keywords
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Journal
CHEMISTRY-A EUROPEAN JOURNAL
Volume 19, Issue 46, Pages 15726-15734
Publisher
Wiley
Online
2013-10-12
DOI
10.1002/chem.201302640
References
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Note: Only part of the references are listed.- Nucleoside-Based Diarylethene Photoswitches and Their Facile Incorporation into Photoswitchable DNA
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- Spiropyran, chromene or spirooxazine ligands: Insights into mutual relations between complexing and photochromic properties
- (2011) Sergey V. Paramonov et al. JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY C-PHOTOCHEMISTRY REVIEWS
- Ring-Closure and Isomerization Capabilities of Spiropyran-Derived Merocyanine Isomers
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- A Light-Driven DNA Nanomachine for the Efficient Photoswitching of RNA Digestion
- (2010) Mengguang Zhou et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Thermal isomerization of spiropyran to merocyanine in aqueous media and its application to colorimetric temperature indication
- (2010) Yasuhiro Shiraishi et al. PHYSICAL CHEMISTRY CHEMICAL PHYSICS
- Synthesis of substituted carbazoles via electrocyclization of in situ generated enamines from 1-phenylsulfonyl-2/(3)-methyl-3/(2)-vinylindoles and DMF·DMA/DMA·DMA
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- Straightforward and Reversible Photoregulation of Hybridization by Using a Photochromic Nucleoside
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- Photoswitched DNA-Binding of a Photochromic Spiropyran
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