STENSRUD, Kenneth F., Dominik HEGER, Peter ŠEBEJ, Jakob WIRZ and Richard S. GIVENS. Fluorinated photoremovable protecting groups: the influence of fluoro substituents on the photo-Favorskii rearrangement. Photochemical & Photobiological Sciences. Cambridge, UK: Royal Society of Chemistry, 2008, vol. 7, No 5, p. 614 - 624, 10 pp. ISSN 1474-905X.
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Basic information
Original name Fluorinated photoremovable protecting groups: the influence of fluoro substituents on the photo-Favorskii rearrangement
Name in Czech Fluorinated photoremovable protecting groups: the influence of fluoro substituents on the photo-Favorskii rearrangement
Authors STENSRUD, Kenneth F. (840 United States of America), Dominik HEGER (203 Czech Republic, guarantor), Peter ŠEBEJ (703 Slovakia), Jakob WIRZ (756 Switzerland) and Richard S. GIVENS (840 United States of America).
Edition Photochemical & Photobiological Sciences, Cambridge, UK, Royal Society of Chemistry, 2008, 1474-905X.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10402 Inorganic and nuclear chemistry
Country of publisher United Kingdom of Great Britain and Northern Ireland
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 2.144
RIV identification code RIV/00216224:14310/08:00025940
Organization unit Faculty of Science
UT WoS 000255743700014
Keywords in English Photoremovable Protecting Group; p-Hydroxyphenacyl Protecting Group; Fluorinated Photoremovable Protecting Groups; Laser Flash Photolysis
Tags Fluorinated Photoremovable Protecting Groups, Laser Flash Photolysis, p-Hydroxyphenacyl Protecting Group, Photoremovable Protecting Group
Tags International impact, Reviewed
Changed by Changed by: doc. Mgr. Dominik Heger, Ph.D., učo 11279. Changed: 7/7/2009 19:26.
Abstract
To further explore the nature of the photo-Favorskii rearrangement and its commitment to substrate photorelease from p-hydroxyphenacyl (pHP), an array of ten new fluorinated pHP gama-aminobutyric acid (GABA) derivatives was synthesized and photolyzed.
Abstract (in Czech)
To further explore the nature of the photo-Favorskii rearrangement and its commitment to substrate photorelease from p-hydroxyphenacyl (pHP), an array of ten new fluorinated pHP gama-aminobutyric acid (GABA) derivatives was synthesized and photolyzed.
Links
MSM0021622413, plan (intention)Name: Proteiny v metabolismu a při interakci organismů s prostředím
Investor: Ministry of Education, Youth and Sports of the CR, Proteins in metabolism and interaction of organisms with the environment
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