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Items: 1 to 20 of 82

1.

BODIPY-derived photoremovable protecting groups unmasked with green light.

Goswami PP, Syed A, Beck CL, Albright TR, Mahoney KM, Unash R, Smith EA, Winter AH.

J Am Chem Soc. 2015 Mar 25;137(11):3783-6. doi: 10.1021/jacs.5b01297. Epub 2015 Mar 17.

PMID:
25751156
2.

In Search of the Perfect Photocage: Structure-Reactivity Relationships in meso-Methyl BODIPY Photoremovable Protecting Groups.

Slanina T, Shrestha P, Palao E, Kand D, Peterson JA, Dutton AS, Rubinstein N, Weinstain R, Winter AH, Klán P.

J Am Chem Soc. 2017 Oct 25;139(42):15168-15175. doi: 10.1021/jacs.7b08532. Epub 2017 Oct 17.

PMID:
29039200
3.

Family of BODIPY Photocages Cleaved by Single Photons of Visible/Near-Infrared Light.

Peterson JA, Wijesooriya C, Gehrmann EJ, Mahoney KM, Goswami PP, Albright TR, Syed A, Dutton AS, Smith EA, Winter AH.

J Am Chem Soc. 2018 Jun 13;140(23):7343-7346. doi: 10.1021/jacs.8b04040. Epub 2018 May 29.

PMID:
29775298
4.

Organelle-Targeted BODIPY Photocages: Visible-Light-Mediated Subcellular Photorelease.

Kand D, Pizarro L, Angel I, Avni A, Friedmann-Morvinski D, Weinstain R.

Angew Chem Int Ed Engl. 2019 Mar 26;58(14):4659-4663. doi: 10.1002/anie.201900850. Epub 2019 Feb 28.

5.

Carbanion-mediated photocages: rapid and efficient photorelease with aqueous compatibility.

Lukeman M, Scaiano JC.

J Am Chem Soc. 2005 Jun 1;127(21):7698-9.

PMID:
15913358
6.

The donor-acceptor biphenyl platform: a versatile chromophore for the engineering of highly efficient two-photon sensitive photoremovable protecting groups.

Specht A, Bolze F, Donato L, Herbivo C, Charon S, Warther D, Gug S, Nicoud JF, Goeldner M.

Photochem Photobiol Sci. 2012 Mar;11(3):578-86. doi: 10.1039/c2pp05360h. Epub 2012 Feb 10.

PMID:
22322902
7.

Applications of p-hydroxyphenacyl (pHP) and coumarin-4-ylmethyl photoremovable protecting groups.

Givens RS, Rubina M, Wirz J.

Photochem Photobiol Sci. 2012 Mar;11(3):472-88. doi: 10.1039/c2pp05399c. Epub 2012 Feb 16. Review.

8.

Photoremovable protecting groups based on electron transfer chemistry.

Falvey DE, Sundararajan C.

Photochem Photobiol Sci. 2004 Sep;3(9):831-8. Epub 2004 Jun 21.

PMID:
15346183
9.

meso-Ester and carboxylic acid substituted BODIPYs with far-red and near-infrared emission for bioimaging applications.

Ni Y, Zeng L, Kang NY, Huang KW, Wang L, Zeng Z, Chang YT, Wu J.

Chemistry. 2014 Feb 17;20(8):2301-10. doi: 10.1002/chem.201303868. Epub 2014 Jan 21.

PMID:
24515608
10.

Dihydronaphthalene-fused boron-dipyrromethene (BODIPY) dyes: insight into the electronic and conformational tuning modes of BODIPY fluorophores.

Wang YW, Descalzo AB, Shen Z, You XZ, Rurack K.

Chemistry. 2010 Mar 1;16(9):2887-903. doi: 10.1002/chem.200902527. Erratum in: Chemistry. 2012 Jun 4;18(23):7306-9.

PMID:
20104551
11.

Fluorescent caged compounds of 2,4-dichlorophenoxyacetic acid (2,4-d): photorelease technology for controlled release of 2,4-D.

Atta S, Jana A, Ananthakirshnan R, Narayana Dhuleep PS.

J Agric Food Chem. 2010 Nov 24;58(22):11844-51. doi: 10.1021/jf1027763. Epub 2010 Oct 25.

PMID:
20973537
12.

Chiral photocages based on phthalimide photochemistry.

Soldevilla A, Griesbeck AG.

J Am Chem Soc. 2006 Dec 27;128(51):16472-3.

PMID:
17177375
13.

A New Photocage Derived from Fluorene.

Reinfelds M, von Cosel J, Falahati K, Hamerla C, Slanina T, Burghardt I, Heckel A.

Chemistry. 2018 Sep 3;24(49):13026-13035. doi: 10.1002/chem.201802390. Epub 2018 Jul 26.

PMID:
29889321
14.

Carbazole substituted boron dipyrromethenes.

Kesavan PE, Gupta I.

Dalton Trans. 2014 Aug 28;43(32):12405-13. doi: 10.1039/c4dt01160k.

PMID:
24999586
15.

Functionalization of boron dipyrrin (BODIPY) dyes through iridium and rhodium catalysis: a complementary approach to alpha- and beta-substituted BODIPYs.

Chen J, Mizumura M, Shinokubo H, Osuka A.

Chemistry. 2009 Jun 8;15(24):5942-9. doi: 10.1002/chem.200802541.

PMID:
19418518
16.

Design and Synthesis of a Calcium-Sensitive Photocage.

Heckman LM, Grimm JB, Schreiter ER, Kim C, Verdecia MA, Shields BC, Lavis LD.

Angew Chem Int Ed Engl. 2016 Jul 11;55(29):8363-6. doi: 10.1002/anie.201602941. Epub 2016 May 24.

17.

Mechanism of the photorelease of alcohols from the 9-phenyl-9-tritylone protecting group.

Zeppuhar AN, Hill-Byrne K, Falvey DE.

Photochem Photobiol Sci. 2019 Aug 1;18(8):1990-1995. doi: 10.1039/c9pp00183b. Epub 2019 Jun 27.

PMID:
31243421
18.

Increasing the dynamic range of metal ion affinity changes in Zn2+ photocages using multiple nitrobenzyl groups.

Gwizdala C, Basa PN, MacDonald JC, Burdette SC.

Inorg Chem. 2013 Aug 5;52(15):8483-94. doi: 10.1021/ic400465g. Epub 2013 Jul 10.

PMID:
23841534
19.

New photoremovable protecting groups for carboxylic acids with high photolytic efficiencies at near-UV irradiation. Application to the photocontrolled release of L-glutamate.

Specht A, Thomann JS, Alarcon K, Wittayanan W, Ogden D, Furuta T, Kurakawa Y, Goeldner M.

Chembiochem. 2006 Nov;7(11):1690-5.

PMID:
16991166
20.

DNA ligation using photoremovable protecting groups.

Kawano Y, Takada T, Nakamura M, Yamana K.

Nucleic Acids Symp Ser (Oxf). 2009;(53):173-4. doi: 10.1093/nass/nrp087.

PMID:
19749316

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