, N You have to login with your ACS ID befor you can login with your Mendeley account. Comprehensive Reviews in Food Science and Food Safety. Recording of Neural Activity With Modulation of Photolysis of Caged Compounds Using Microelectrode Arrays in Rats With Seizures. Photocontrol of Protein Activity in Cultured Cells and Zebrafish with One- and Two-Photon Illumination. Light Control of Cellular Processes by Using Photocaged Abscisic Acid. A Synthesis, Wiley-Interscience, New York, 1999, 372-381, 415-419, Fluorescent Ligands and Energy Transfer in Photoactive Ruthenium–Bipyridine Complexes. Ryan W Lewis, George P Hess, Bruce Ganem. Please reconnect. Deepak Kumar Sinha, Pierre Neveu, Nathalie Gagey, Isabelle Aujard, Chouaha Benbrahim-Bouzidi, Thomas Le Saux, Christine Rampon, Carole Gauron, Bernard Goetz, Sylvie Dubruille, Marc Baaden, Michel Volovitch, David Bensimon, Sophie Vriz, Ludovic Jullien. The caged compound has a major absorption band with a maximum at 390 nm (ε390 = 13651 M-1 cm-1). Naoko Senda, Atsuya Momotake, Tatsuo Arai. Alexander G. Russell, Maria-Eleni Ragoussi, Rui Ramalho, Christopher W. Wharton, David Carteau, Dario M. Bassani and John S. Snaith . Coumarinylmethyl Caging Groups with Redshifted Absorption. receptor mechanism and function. Photolabile Glutamate Protecting Group with High One- and Two-Photon Uncaging Efficiencies. Olivier Galangau, Stéphanie Delbaere, Nicolas Ratel-Ramond, Gwénaël Rapenne, Ruiji Li, Jan Patrick Dela Cruz Calupitan, Takuya Nakashima, and Tsuyoshi Kawai . Common diols used to form ketals are show below in order of their relative rate of formation. Minoru Yamaji, Koichi Nozaki, Xavier Allonas, Satoru Nakajima, Shozo Tero-Kubota and Bronislaw Marciniak. ) polypyridine complexes of indolamines. Transient photocyclization in ruthenium( Fernandes, M. Sameiro T. Gonçalves, Susana P.G. 2-( Benoît Briand, Nico Kotzur, Volker Hagen, Michael Beyermann. Richard S. Givens, Marina Rubina, Jakob Wirz. Maral Seidi Damyeh, Ram Mereddy, Michael E. Netzel, Yasmina Sultanbawa. 728-731. Light-Triggered Thiol-Exchange on Gold Nanoparticles at Low Micromolar Concentrations in Water. Petra Stegmaier, José María Alonso and Aránzazu del Campo . Seiji Sakamoto, Mika Terauchi, Yasuyuki Araki, Takehiko Wada. A new synthesis of caged GABA compounds for studying GABAA receptors. Development of novel water-soluble photocleavable protective group and its application for design of photoresponsive paclitaxel prodrugs. Ludovic Fournier, Isabelle Aujard, Thomas Le Saux, Sylvie Maurin, Sandra Beaupierre, Jean‐Bernard Baudin, Ludovic Jullien. Find more information on the Altmetric Attention Score and how the score is calculated. Spectral Evolution of a Photochemical Protecting Group for Orthogonal Two-Color Uncaging with Visible Light. Florica Adriana Jerca, Valentin Victor Jerca, Izabela-Cristina Stancu. Unlike previously used caging groups for carboxylic acids, it can be photolyzed rapidly and efficiently in the visible wavelength region. The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. T. W. Green, P. G. M. Wuts, Protective Groups in Organic 1-(Hydroxyacetyl)pyrene a new fluorescent phototrigger for cell imaging and caging of alcohols, phenol and adenosine. Simone Weis, Zahid Shafiq, Radu A. Gropeanu, Aránzazu del Campo. -Acyl- ) polypyridyl complexes as photocages for bioactive compounds containing nitriles and aromatic heterocycles. Fei Gao, Xinxia Cai, Guihua Xiao, Yilin Song, Mixia Wang, Ziyue Li, Yu Zhang, Shengwei Xu, Jingyu Xie, Huabing Yin. Applications of p-hydroxyphenacyl (pHP) and coumarin-4-ylmethyl photoremovable protecting groups. T. W. Green, P. G. M. Wuts, Protective Groups in Organic Dual Photochemical Bond Cleavage for a Diarylethene-Based Phototrigger Containing both Methanolic and Acetic Sources. ii Alkyl esters: Cleavage: Formation: Fischer esterification (RCOOH + R’OH + H+) Acid chloride + ROH, pyridine t-Butyl esters: Isobutylene & acid Methyl esters: Diazomethane LiOH, THF, H 2O Richard H Kramer, Doris L Fortin, Dirk Trauner. Building Biomedical Materials using Photochemical Bond Cleavage. Youhei Sohma, Taku Yoshiya, Atsuhiko Taniguchi, Tooru Kimura, Yoshio Hayashi, Yoshiaki Kiso. A protective group (also referred to as "protecting group") is a reversably formed derivative of an existing functional group in a molecule. A New Inorganic Photolabile Protecting Group for Highly Efficient Visible Light GABA Uncaging. These metrics are regularly updated to reflect usage leading up to the last few days. Functionalized photo-responsive polymeric system. Photorelease of Carboxylic Acids Mediated by Visible-Light-Absorbing Gold-Nanoparticles. IEEE Transactions on Biomedical Engineering. 728-731. Pivalic acid ester: Benzoic acid ester : 1,2-; 1,3-Diols: Acetonide: Benzylidene acetal >> Stability: What are protective groups? Kavita Bhagat, Jatinder V. Singh, Piyusha P. Pagare, Nitish Kumar, Anchal Sharma, Gurinder Kaur, Nihar Kinarivala, Srinivasa Gandu, Harbinder Singh, Sahil Sharma, Preet Mohinder S. Bedi. In vivo photorelease of GABA in the mouse cortex. Maria J.G. A Protecting Group for Carboxylic Acids That Can Be Photolyzed by Visible Light, Department of Molecular Biology and Genetics, 216 Biotechnology Building, Cornell University, Ithaca, New York 14853-2703, and Department of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14853-2703. Unlike previously used caging groups for carboxylic acids, it can be photolyzed rapidly and efficiently in the visible wavelength region. Find more information about Crossref citation counts. Experiments are performed at 400 nm (ε400 = 12232 M-1 cm-1) and longer wavelengths. Article Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. Alexandre Specht, Jean-Sébastien Thomann, Karine Alarcon, Weerawut Wittayanan, David Ogden, Toshiaki Furuta, Yuji Kurakawa, Maurice Goeldner. 2-Oxo-2H-benzo[h]benzopyran as a new light sensitive protecting group for neurotransmitter amino acids. M. Arfan Ashraf, Alexander G. Russell, Christopher W. Wharton, John S. Snaith. Tadamitsu Sakurai, Koh Watanabe, Shun Takahashi, Takuya Yoshizawa, Tetsutaro Igarashi. “Click Peptide” Based on the “O-Acyl Isopeptide Method”:  Control of Aβ1−42 Production from a Photo-Triggered Aβ1−42 Analogue. Petr Klán, Tomáš Šolomek, Christian G. Bochet, Aurélien Blanc, Richard Givens, Marina Rubina, Vladimir Popik, Alexey Kostikov, and Jakob Wirz . Chromophores for the Delivery of Bioactive Molecules with Two-Photon Excitation. Cyril Herbivo, Ziad Omran, Julia Revol, Hélène Javot, Alexandre Specht. N-Acyl-N-carboxymethyl-2-nitroaniline and its analogues: a new class of water-soluble photolabile precursor of carboxylic acids. • Benzyl esters – Removed by hydrogenolysis. Effect of fluorescent whitening agent on the transcription of cell damage-related genes in zebrafish embryos. Journal of Photochemistry and Photobiology A: Chemistry. Hyun Jung, Seung-Hyeok Seok, Ju-Hee Han, Tamer Said Abdelkader, Tae-Hyoun Kim, Seo-Na Chang, Ae-Sun Ko, Seung-Kyu Choi, Cho-Rong Lee, Ji-Eun Seo, Soo-Hyun Byun, Jung-A Kim, Jae-Hak Park.

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