Facile and environmentally friendly halogenation of BODIPYs in deep eutectic solvent

[1]  François Jérôme,et al.  Bio-based solvents: an emerging generation of fluids for the design of eco-efficient processes in catalysis and organic chemistry. , 2013, Chemical Society reviews.

[2]  M. Vendrell,et al.  Multicomponent reactions for de novo synthesis of BODIPY probes: in vivo imaging of phagocytic macrophages. , 2013, Journal of the American Chemical Society.

[3]  K. Burgess,et al.  Double-targeting using a TrkC ligand conjugated to dipyrrometheneboron difluoride (BODIPY) based photodynamic therapy (PDT) agent. , 2013, Journal of medicinal chemistry.

[4]  Zilong Wang,et al.  Intramolecular RET enhanced visible light-absorbing bodipy organic triplet photosensitizers and application in photooxidation and triplet-triplet annihilation upconversion. , 2013, Journal of the American Chemical Society.

[5]  Jianzhang Zhao,et al.  Bodipy derivatives as organic triplet photosensitizers for aerobic photoorganocatalytic oxidative coupling of amines and photooxidation of dihydroxylnaphthalenes. , 2013, The Journal of organic chemistry.

[6]  Yixing Wang,et al.  A new practical and highly efficient iodination of BODIPY derivatives with hypervalent iodine reagent , 2012 .

[7]  W. Dehaen,et al.  Synthesis of meso-halogenated BODIPYs and access to meso-substituted analogues. , 2012, Organic letters.

[8]  Burkhard König,et al.  Low melting mixtures in organic synthesis – an alternative to ionic liquids? , 2012 .

[9]  François Jérôme,et al.  Deep eutectic solvents: syntheses, properties and applications. , 2012, Chemical Society reviews.

[10]  D. Ramaiah,et al.  Aza-BODIPY derivatives: enhanced quantum yields of triplet excited states and the generation of singlet oxygen and their role as facile sustainable photooxygenation catalysts. , 2012, Chemistry.

[11]  X. Jing,et al.  Porous heterogeneous organic photocatalyst prepared by HIPE polymerization for oxidation of sulfides under visible light , 2012 .

[12]  Samad Khaksar,et al.  Transition metal-free oxidation of activated alcohols to aldehydes and ketones in 1,1,1,3,3,3-hexafluoro-2-propanol , 2012 .

[13]  Samad Khaksar,et al.  A simple, efficient and green procedure for the synthesis of bis-indolyl methanes in 1,1,1,3,3,3-hexafluoro-2-propanol , 2012 .

[14]  W. Dehaen,et al.  Fluorescent indicators based on BODIPY. , 2012, Chemical Society reviews.

[15]  W. Dehaen,et al.  2- and 3-Monohalogenated BODIPY Dyes and Their Functionalized Analogues: Synthesis and Spectroscopy , 2011 .

[16]  Lynn F. Gladden,et al.  Glycerol eutectics as sustainable solvent systems , 2010 .

[17]  J. Tour,et al.  Synthesis of highly fluorescent BODIPY-based nanocars. , 2010, Organic letters.

[18]  W. Dehaen,et al.  A versatile, modular synthesis of monofunctionalized BODIPY dyes. , 2009, Chemical communications.

[19]  M. Ratnikov,et al.  Lewis acid catalyst free electrophilic alkylation of silicon-capped pi donors in 1,1,1,3,3,3-hexafluoro-2-propanol. , 2008, Angewandte Chemie.

[20]  G. Ulrich,et al.  Tailoring the properties of boron-dipyrromethene dyes with acetylenic functions at the 2,6,8 and 4-B substitution positions. , 2008, Organic letters.

[21]  Anthony Harriman,et al.  The chemistry of fluorescent bodipy dyes: versatility unsurpassed. , 2008, Angewandte Chemie.

[22]  T. Dohi,et al.  First hypervalent iodine(III)-catalyzed C-N bond forming reaction: catalytic spirocyclization of amides to N-fused spirolactams. , 2007, Chemical communications.

[23]  W. Dehaen,et al.  Functionalisation of fluorescent BODIPY dyes by nucleophilic substitution. , 2006, Chemical communications.

[24]  E. Akkaya,et al.  Water soluble distyryl-boradiazaindacenes as efficient photosensitizers for photodynamic therapy. , 2006, Chemical communications.

[25]  David Beljonne,et al.  A highly potassium-selective ratiometric fluorescent indicator based on BODIPY azacrown ether excitable with visible light. , 2005, Organic letters.

[26]  Y. Urano,et al.  Highly efficient and photostable photosensitizer based on BODIPY chromophore. , 2005, Journal of the American Chemical Society.

[27]  Yan Zhang,et al.  An Efficient and ConvenientBromination of BODIPY Derivatives with Copper(II) Bromide , 2012 .