Synthesis and Photophysical Properties of C3‐Symmetric Star‐Shaped Molecules Containing Heterocycles: A New Tactics for Multiple Fischer Indolization
暂无分享,去创建一个
[1] S. Kotha,et al. Application of Fischer Indolization under Green Conditions using Deep Eutectic Solvents. , 2017, Chemical record.
[2] Bin Yao,et al. A Star-Shaped Molecule with Low-Lying Lowest Unoccupied Molecular Orbital Level, n-Type Panchromatic Electrochromism, and Long-Term Stability. , 2017, Organic letters.
[3] T. Khan,et al. Impact of Molecular Arrangement and Torsional Motion on the Fluorescence of Salophen and Its Metal Complexes , 2017 .
[4] M. A. Pericàs,et al. Synthesis and catalytic applications of C3-symmetric tris(triazolyl)methanol ligands and derivatives. , 2016, Chemical communications.
[5] T. Yamaguchi,et al. A durable anion conducting membrane with packed anion-exchange sites and an aromatic backbone for solid-state alkaline fuel cells , 2015 .
[6] B. Sridhar,et al. Conformationally Flexible C3-Symmetric 1,3-Oxazoles as Molecular Scaffolds , 2015 .
[7] S. Kotha,et al. Diversity-Oriented Approach to Cyclophanes via Fischer Indolization and Ring-Closing Metathesis: Substrate-Controlled Stereochemical Outcome in RCM. , 2015, The Journal of organic chemistry.
[8] A. R. Fernandes,et al. Heterocyclic Anticancer Compounds: Recent Advances and the Paradigm Shift towards the Use of Nanomedicine’s Tool Box , 2015, Molecules.
[9] S. Kotha,et al. Design and synthesis of hybrid cyclophanes containing thiophene and indole units via Grignard reaction, Fischer indolization and ring-closing metathesis as key steps , 2015, Beilstein journal of organic chemistry.
[10] Zhi-qiang Liu,et al. Octupolar (C3 and S4) Symmetric Cyclized Indole Derivatives: Syntheses, Structures, and NLO Properties. , 2015, Organic letters.
[11] H. Reissig,et al. C3-Symmetric Pyridine and Bipyridine Derivatives: Simple Preparation by Cyclocondensation and 2D Self-Assembly at a Solution–Graphite Interface , 2015 .
[12] Yan‐Chao Wu,et al. Rearrangement of dypnones to 1,3,5-triarylbenzenes. , 2015, Organic letters.
[13] M. Shibata,et al. Synthesis and properties of novel C3-symmetrical 1,3,5-tris(dibenzoheterolyl)benzenes , 2015 .
[14] Emma L. Smith,et al. Deep eutectic solvents (DESs) and their applications. , 2014, Chemical reviews.
[15] S. Martin,et al. Enantioselective Total Syntheses of Citrinadins A and B. Stereochemical Revision of Their Assigned Structures , 2014, Journal of the American Chemical Society.
[16] Po-Chiao Lin,et al. Synthesis of substituted 3-indolylimines and indole-3-carboxaldehydes by rhodium(II)-catalyzed annulation. , 2014, Organic letters.
[17] Scott J. Miller,et al. Total synthesis and isolation of citrinalin and cyclopiamine congeners , 2014, Nature.
[18] W. Skene,et al. Conjugated C3 symmetric aryl tripyrroles and aryl bipyrroles: synthesis, optical and electronic properties , 2014 .
[19] Wenjun Zhang,et al. Synthesis and photovoltaic properties of solution-processable star-shaped small molecules with triphenylamine as the core and alkyl cyanoacetate or 3-ethylrhodanine as the end-group , 2014 .
[20] Sambasivarao Kotha,et al. Diversity-oriented approaches to unusual α-amino acids and peptides: step economy, atom economy, redox economy, and beyond. , 2013, The Journal of organic chemistry.
[21] P. Stavrinou,et al. Location, Location, Location ‐ Strategic Positioning of 2,1,3‐Benzothiadiazole Units within Trigonal Quaterfluorene‐Truxene Star‐Shaped Structures , 2013 .
[22] Jae Kwan Lee,et al. Planar star-shaped organic semiconductor with fused triphenylamine core for solution-processed small-molecule organic solar cells and field-effect transistors. , 2012, Organic letters.
[23] Burkhard König,et al. Low melting mixtures in organic synthesis – an alternative to ionic liquids? , 2012 .
[24] B. König,et al. Fischer indole synthesis in low melting mixtures. , 2012, Organic letters.
[25] A. Terec,et al. Synthesis and Structural Analysis of Some Podands with C3 Symmetry , 2012 .
[26] Mobin M. Shaikh,et al. Diversity-oriented approach to macrocyclic cyclophane derivatives by Suzuki-Miyaura cross-coupling and olefin metathesis as key steps. , 2012, The Journal of organic chemistry.
[27] M. Greaney,et al. The benzyne Fischer-indole reaction. , 2011, Organic letters.
[28] I. Osaka,et al. Synthesis and characterization of benzo[1,2-b:3,4-b':5,6-b'']trithiophene (BTT) oligomers. , 2011, The Journal of organic chemistry.
[29] M. Iyoda,et al. Star-shaped oligothiophenes with unique photophysical properties and nanostructured polymorphs. , 2010, Chemistry.
[30] M. Pasquali,et al. Mono- and Biexponential Luminescence Decays of Individual Single-Walled Carbon Nanotubes , 2010 .
[31] F. Hof,et al. A tryptophan-analog host whose interactions with ammonium ions in water are dominated by the hydrophobic effect , 2009 .
[32] J. Joo,et al. Photoreactive π-conjugated star-shaped molecules for the organic field-effect transistor , 2009 .
[33] K. Mandal,et al. A retrospective on the design and synthesis of novel molecules through a strategic consideration of metathesis and Suzuki-Miyaura cross-coupling. , 2009, Chemistry, an Asian journal.
[34] Sandeep Kumar,et al. Synthesis of liquid crystalline materials based on 1,3,5-triphenylbenzene and 2,4,6-triphenyl-1,3,5-s-triazine , 2008 .
[35] T. Konakahara,et al. InBr3-promoted divergent approach to polysubstituted indoles and quinolines from 2-ethynylanilines: switch from an intramolecular cyclization to an intermolecular dimerization by a type of terminal substituent group. , 2008, The Journal of organic chemistry.
[36] R. Cooks,et al. Organic reactions of ionic intermediates promoted by atmospheric-pressure thermal activation. , 2008, Angewandte Chemie.
[37] Wenyong Lai,et al. Kinked Star‐Shaped Fluorene/ Triazatruxene Co‐oligomer Hybrids with Enhanced Functional Properties for High‐Performance, Solution‐Processed, Blue Organic Light‐Emitting Diodes , 2008 .
[38] K. Kreger,et al. Combinatorial Development of Blue OLEDs Based on Star Shaped Molecules , 2007 .
[39] Yunjeong Kim,et al. A Porous and Interpenetrated Metal–Organic Framework Comprising Tetranuclear IronIII–Oxo Clusters and Tripodal Organic Carboxylates and Its Implications for (3,8)-Coordinated Networks , 2007 .
[40] Su Jin Kim,et al. Soluble Star-Shaped Molecules Based on Thiophene Derivatives as Organic Semiconductors for Field-Effect Transistor Applications , 2007 .
[41] K. Mandal,et al. Formation of arenes via diallylarenes : Strategic utilization of suzuki-miyaura cross-coupling, claisen rearrangement and ring-closing metathesis , 2007 .
[42] S. Kotha,et al. Expanding the Diversity of Polycyclic Aromatics Through a Suzuki–Miyaura Cross‐Coupling Strategy , 2007 .
[43] A. Mourran,et al. Star-Shaped Oligothiophenes for Solution-Processible Organic Electronics: Flexible Aliphatic Spacers Approach , 2006 .
[44] Jeffrey T. Kuethe,et al. Practical methodologies for the synthesis of indoles. , 2006, Chemical reviews.
[45] P. Bäuerle,et al. Star-shaped perylene–oligothiophene–triphenylamine hybrid systems for photovoltaic applications , 2006 .
[46] Jean Roncali,et al. Triphenylamine-thienylenevinylene hybrid systems with internal charge transfer as donor materials for heterojunction solar cells. , 2006, Journal of the American Chemical Society.
[47] P. Eilbracht,et al. 2,3-Disubstituted indoles from olefins and hydrazines via tandem hydroformylation-Fischer indole synthesis and skeletal rearrangement. , 2006, Organic & biomolecular chemistry.
[48] S. Kotha,et al. A Simple Synthetic Approach to Allylated Aromatics via the Suzuki-Miyaura Cross-Coupling Reaction , 2005 .
[49] Jieping Zhu,et al. Microwave-assisted intramolecular Suzuki-Miyaura reaction to macrocycle, a concise asymmetric total synthesis of biphenomycin B. , 2005, Organic letters.
[50] Jin-Hyun Jeong,et al. Synthesis of 2,3-disubstituted indole on solid phase by the Fischer indole synthesis. , 2005, Journal of combinatorial chemistry.
[51] R. B. Sunoj,et al. Synthesis of C3‐Symmetric Nano‐Sized Polyaromatic Compounds by Trimerization and Suzuki−Miyaura Cross‐Coupling Reactions , 2004 .
[52] H. Sharghi,et al. Reactions on a solid surface. A simple, economical and efficient Friedel-Crafts acylation reaction over zinc oxide (ZnO) as a new catalyst. , 2004, The Journal of organic chemistry.
[53] A. Echavarren,et al. Synthesis of a triaza analogue of crushed-fullerene by intramolecular palladium-catalyzed arylation. , 2004, Organic letters.
[54] Michael G Debije,et al. The optical and charge transport properties of discotic materials with large aromatic hydrocarbon cores. , 2004, Journal of the American Chemical Society.
[55] A. Elschner,et al. Star‐Shaped Oligothiophenes for Solution‐Processible Organic Field‐Effect Transistors , 2003 .
[56] M. Thelakkat. Star-shaped, dendrimeric and polymeric triarylamines as photoconductors and hole transport materials for electro-optical applications , 2002 .
[57] S. Kotha,et al. A new approach for modification of phenylalanine peptides by Suzuki-Miyaura coupling reaction. , 2001, Bioorganic & medicinal chemistry letters.
[58] H. L. Carrell,et al. Shape and Size Effects in the Crystal Structures of Complexes of 1,3,5-Trinitrobenzene with some Trigonal Donors: The Benzene–Thiophene Exchange Rule , 2000 .
[59] S. Kotha,et al. A General and Simple Method for the Synthesis of Star-Shaped Thiophene Derivatives , 1999 .
[60] C. Moberg. C3 Symmetry in Asymmetric Catalysis and Chiral Recognition. , 1998, Angewandte Chemie.
[61] V. Tsukruk,et al. Columnar discotics for light emitting diodes , 1997 .
[62] P. Schuhmacher,et al. Fast photoconduction in the highly ordered columnar phase of a discotic liquid crystal , 1994, Nature.
[63] P. Batail,et al. Tetrathiafulvalene- and dithiafulvene-substituted mesitylenes, new π-donor molecules with 3-fold symmetry and the formation of an unprecedented new class of electroactive polymers , 1993 .
[64] H. Sugano,et al. Synthesis and central nervous system actions of thyrotropin-releasing hormone analogs containing a 1-oxo-1,2,3,4-tetrahydroisoquinoline moiety. , 1988, Chemical & pharmaceutical bulletin.
[65] István Hargittai,et al. Symmetry through the eyes of a chemist , 1986 .
[66] J. Groves. The Friedel–Crafts acylation of alkenes , 1972 .