Synthesis and evaluation of new caged compound with thiochromone derivative

[1]  K. Kakiuchi,et al.  A novel thiochromone-type photolabile protecting group for carbonyl compounds , 2013 .

[2]  R. Givens,et al.  Photoremovable Protecting Groups in Chemistry and Biology: Reaction Mechanisms and Efficacy , 2012, Chemical reviews.

[3]  K. Kakiuchi,et al.  Synthesis and characterization of thiochromone S,S-dioxides as new photolabile protecting groups. , 2008, Chemical communications.

[4]  G. Ellis‐Davies,et al.  Caged compounds: photorelease technology for control of cellular chemistry and physiology , 2007, Nature Methods.

[5]  D. Ogden,et al.  Photorelease of Carboxylic Acids from 1-Acyl-7-nitroindolines in Aqueous Solution: Rapid and Efficient Photorelease of l-Glutamate1 , 1999 .

[6]  R. Givens,et al.  New Photoactivated Protecting Groups. 7.p-Hydroxyphenacyl: A Phototrigger for Excitatory Amino Acids and Peptides1 , 1997 .

[7]  George J Augustine,et al.  Chemical Two-Photon Uncaging: a Novel Approach to Mapping Glutamate Receptors , 1997, Neuron.

[8]  R. Givens,et al.  New Photoactivated Protecting Groups. 6. p-Hydroxyphenacyl: A Phototrigger for Chemical and Biochemical Probes1,2 , 1997 .

[9]  E. Callaway,et al.  Photostimulation using caged glutamate reveals functional circuitry in living brain slices. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[10]  J. Kaplan,et al.  Rapid photolytic release of adenosine 5'-triphosphate from a protected analogue: utilization by the Na:K pump of human red blood cell ghosts. , 1978, Biochemistry.

[11]  W. D. Mcelroy,et al.  Stereo-specificity and firefly bioluminescence, a comparison of natural and synthetic luciferins. , 1961, Proceedings of the National Academy of Sciences of the United States of America.

[12]  G. P. Hess,et al.  Development and application of caged ligands for neurotransmitter receptors in transient kinetic and neuronal circuit mapping studies. , 1998, Methods in enzymology.