Research graph
References from Long-wavelength photoremovable protecting groups: On the way to in vivo application. Local targets link to admitted publications; unresolved targets remain external evidence.
Light in diagnosis, therapy and surgery
2017 · External reference
10.1021/acs.chemrev.8b00037
10.1021/acs.chemrev.8b00037 · External reference
10.1002/wnan.1450
10.1002/wnan.1450 · External reference
Synthesis, structure, and reactivity of adenosine cyclic 3’,5’-phosphate-benzyltriesters
10.1021/jm00217a008 · 1977 · External reference
Rapid photolytic release of adenosine 5’-triphosphate from a protected analog: utilization by the sodium:potassium pump of human red blood cell ghosts
10.1021/bi00603a020 · 1978 · External reference
10.1021/cr300177k
10.1021/cr300177k · External reference
Why develop photoactivated chemotherapy?
2003 · External reference
Unresolved reference
External reference
10.1248/cpb.c16-00403
10.1248/cpb.c16-00403 · External reference
A yellowish-green-light-controllable nitric oxide donor based on N-nitrosoaminophenol applicable for photocontrolled vasodilation
10.1039/c7ob00245a · 2017 · External reference
Structure-efficiency relationship of photoinduced electron transfer-triggered nitric oxide releasers
10.1038/s41598-018-38252-5 · 2019 · External reference
Review of a potential novel approach for erectile dysfunction: light-controllable nitric oxide donors and nanoformulations
2019 · External reference
A photocalibrated NO donor based on N-nitrosorhodamine 6G upon UV irradiation
10.1016/j.cclet.2018.03.011 · 2019 · External reference
10.1021/acs.analchem.7b04510
10.1021/acs.analchem.7b04510 · External reference
10.1021/acs.bioconjchem.7b00821
10.1021/acs.bioconjchem.7b00821 · External reference
Photomanipulation of vasodilation with a blue-light-controllable nitric oxide releaser
10.1021/ja5020053 · 2014 · External reference
A molecular hybrid producing simultaneously singlet oxygen and nitric oxide by single photon excitation with green light
10.1016/j.bioorg.2018.12.027 · 2019 · External reference
Fluorescent nitric oxide photodonors based on BODIPY and rhodamine antennae
10.1002/chem.201902062 · 2019 · External reference
Near-infrared photoactivatable nitric oxide donors with integrated photoacoustic monitoring
10.1021/jacs.8b05514 · 2018 · External reference
Tunable visible and near-IR photoactivation of light-responsive compounds by using fluorophores as light-capturing antennas
10.1002/anie.201308816 · 2014 · External reference
Vitamin B12: a tunable, long wavelength, light-responsive platform for launching therapeutic agents
10.1021/acs.accounts.5b00331 · 2015 · External reference
Cobalt-carbon homolysis and bond dissociation energy studies of biological alkylcobalamins: methylcobalamin, including a.gtoreq.1015 Co-CH3 homolysis rate enhancement at 25.degree. following one-electron reduction
10.1021/ja00162a053 · 1990 · External reference
10.1021/acs.orglett.8b00100
10.1021/acs.orglett.8b00100 · External reference
A general strategy for visible-light decaging based on the quinone trimethyl lock
10.1021/jacs.7b01548 · 2017 · External reference
A general strategy for visible-light decaging based on the quinone cis-alkenyl lock
10.1039/c9cc01073d · 2019 · External reference
Near-IR photochemistry for biology: exploiting the optical window of tissue
10.1111/php.13068 · 2019 · External reference
Photoactivation of amino-substituted 1,4-benzoquinones for release of carboxylate and phenolate leaving groups using visible light
10.1021/jo060790g · 2006 · External reference
Mechanistic studies of the photoinduced quinone trimethyl lock decaging process
10.1021/jacs.6b12007 · 2017 · External reference
Boron dipyrromethene as a fluorescent caging group for single-photon uncaging with long-wavelength visible light
10.1021/cb500525p · 2014 · External reference
Transition-metal-free CO-releasing BODIPY derivatives activatable by visible to NIR light as promising bioactive molecules
10.1021/jacs.5b10800 · 2016 · External reference
Family of BODIPY photocages cleaved by single photons of visible/near-infrared light
10.1021/jacs.8b04040 · 2018 · External reference
10.1021/jacs.5b01297
10.1021/jacs.5b01297 · External reference
In search of the perfect photocage: structure-reactivity relationships in meso-methyl BODIPY photoremovable protecting groups
10.1021/jacs.7b08532 · 2017 · External reference
Construction of the carbon–chalcogen (S, Se, Te) bond at the 2,6-positions of BODIPY via Stille cross-coupling reaction
10.1039/c6cc06923a · 2016 · External reference
Coumarin photocaging groups modified with an electron-rich styryl moiety at the 3-position: long-wavelength excitation, rapid photolysis, and photobleaching
10.1002/anie.201800713 · 2018 · External reference
10.1021/ja5065203
10.1021/ja5065203 · External reference
Harnessing cyanine photooxidation: from slowing photobleaching to near-IR uncaging
10.1016/j.cbpa.2016.05.022 · 2016 · External reference
Cyanine modification tuned for amine photorelease
10.1111/php.13102 · 2019 · External reference
A cyanine photooxidation/β-elimination sequence enables near-infrared uncaging of aryl amine payloads
10.1111/php.13090 · 2019 · External reference
In vivo activation of duocarmycin-antibody conjugates by near-infrared light
10.1021/acscentsci.7b00026 · 2017 · External reference
Near-IR light-mediated cleavage of antibody-drug conjugates using cyanine photocages
10.1002/anie.201507391 · 2015 · External reference
Near-infrared uncaging or photosensitizing dictated by oxygen tension
10.1038/ncomms13378 · 2016 · External reference
Caged compounds for two-photon uncaging
10.1016/b978-0-12-409547-2.13667-4 · 2018 · External reference
10.1364/ome.6.001679
10.1364/ome.6.001679 · External reference
10.1021/acs.chemrev.8b00253
10.1021/acs.chemrev.8b00253 · External reference
10.1021/cn100052v
10.1021/cn100052v · External reference
10.1002/cplu.201900139
10.1002/cplu.201900139 · External reference
The donor–acceptor biphenyl platform: a versatile chromophore for the engineering of highly efficient two-photon sensitive photoremovable protecting groups
10.1039/c2pp05360h · 2012 · External reference
10.1021/jo501425p
10.1021/jo501425p · External reference
Design and synthesis of a 4-nitrobromobenzene derivative bearing an ethylene glycol tetraacetic acid unit for a new generation of caged calcium compounds with two-photon absorption properties in the near-IR region and their application in vivo
10.1021/acsomega.6b00119 · 2016 · External reference
10.1039/c7sc05182d
10.1039/c7sc05182d · External reference
Design and synthesis of a new chromophore, 2-(4-nitrophenyl)benzofuran, for two-photon uncaging using near-IR light
10.1039/c5cc07664a · 2015 · External reference
Two-photon sensitive protecting groups operating via intramolecular electron transfer: uncaging of GABA and tryptophan
10.1039/c4sc03775h · 2015 · External reference
10.1002/chem.201601109
10.1002/chem.201601109 · External reference
Two-photon “caging” groups: effect of position isomery on the photorelease properties of aminoquinoline-derived photolabile protecting groups
10.1021/ol5035035 · 2015 · External reference
10.1021/acs.orglett.7b00957
10.1021/acs.orglett.7b00957 · External reference
Optically selective two-photon uncaging of glutamate at 900 nm
10.1021/ja4019379 · 2013 · External reference
Dual-wavelength efficient two-photon photorelease of glycine by π-extended dipolar coumarins
10.1039/c9sc00148d · 2019 · External reference
10.1021/acsnano.5b01573
10.1021/acsnano.5b01573 · External reference
10.1007/978-981-10-1590-8_13
10.1007/978-981-10-1590-8_13 · External reference
10.1039/c6cc03864f
10.1039/c6cc03864f · External reference
10.1021/jacs.5b11606
10.1021/jacs.5b11606 · External reference
10.1002/anie.201906067
10.1002/anie.201906067 · External reference
