Exploring the influence of designer surfactant hydrophobicity in key C C/C N bond forming reactions

[1]  J. Mestan,et al.  5-(4,6-Dimorpholino-1,3,5-triazin-2-yl)-4-(trifluoromethyl)pyridin-2-amine (PQR309), a Potent, Brain-Penetrant, Orally Bioavailable, Pan-Class I PI3K/mTOR Inhibitor as Clinical Candidate in Oncology. , 2017, Journal of medicinal chemistry.

[2]  F. Gallou,et al.  Micellar catalysis-enabled sustainable ppm Au-catalyzed reactions in water at room temperature† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c7sc02405c Click here for additional data file. , 2017, Chemical science.

[3]  B. Lipshutz The ‘Nano-to-Nano’ Effect Applied to Organic Synthesis in Water , 2017 .

[4]  K. Ahmed,et al.  Stearyl MethoxyPEGglycol Succinate—A Designer Micellar Medium for Diverse Aniline Derivatives Synthesis , 2017 .

[5]  Sengan Megarajan,et al.  Synthesis, characterization, and determination of critical micellar concentration and thermotropic phase transition of taurolipids , 2017 .

[6]  M. Parmentier,et al.  Sustainable and Scalable Fe/ppm Pd Nanoparticle Nitro Group Reductions in Water at Room Temperature , 2017 .

[7]  Vijay Luxami,et al.  Synthesis and in vitro evaluation of novel triazine analogues as anticancer agents and their interaction studies with bovine serum albumin , 2016 .

[8]  S. Sobhani,et al.  A new magnetically recoverable heterogeneous palladium catalyst for phosphonation reactions in aqueous micellar solution , 2016 .

[9]  Tom Welton,et al.  Solvents and sustainable chemistry , 2015, Proceedings of the Royal Society A: Mathematical, Physical and Engineering Sciences.

[10]  K. Mukkanti,et al.  A Pd-catalyzed direct entry to 11-substituted 6H-isoindolo[2,1-a]indol-6-one derivatives as potential anticancer agents , 2015 .

[11]  F. Gallou,et al.  Nucleophilic Aromatic Substitution Reactions in Water Enabled by Micellar Catalysis. , 2015, Organic letters.

[12]  Marina Cvjetko Bubalo,et al.  Green Solvents for Green Technologies , 2015 .

[13]  B. Lipshutz,et al.  Reductions of aryl bromides in water at room temperature. , 2015, Tetrahedron letters.

[14]  Xichen Lin,et al.  Efficient and C2-selective arylation of indoles, benzofurans, and benzothiophenes with iodobenzenes in water at room temperature , 2015 .

[15]  J. D. Elliott,et al.  A mild and efficient carboxylate-directed C–H arylation of aryl carboxylic acids with iodobenzenes in water , 2015 .

[16]  Anbazhagan Veerappan,et al.  Activity of catalytic silver nanoparticles modulated by capping agent hydrophobicity. , 2014, Colloids and surfaces. B, Biointerfaces.

[17]  Marcos D. García,et al.  Metallacycle-catalyzed SNAr reaction in water: supramolecular inhibition by means of host–guest complexation. , 2014, The Journal of organic chemistry.

[18]  Yufeng Du,et al.  The regioselective Larock indole synthesis catalyzed by NHC–palladium complexes , 2013 .

[19]  G. Helguera,et al.  “True” Hydrophilic-Lipophilic Balance of Polyoxyethylene Fatty Acid Esters Nonionic Surfactants , 2013 .

[20]  B. Lipshutz,et al.  Catalysis in the Service of Green Chemistry: Nobel Prize-Winning Palladium-Catalysed Cross-Couplings, Run in Water at Room Temperature: Heck, Suzuki-Miyaura and Negishi reactions carried out in the absence of organic solvents, enabled by micellar catalysis. , 2012, Platinum metals review.

[21]  B. Lipshutz,et al.  TPGS-750-M: a second-generation amphiphile for metal-catalyzed cross-couplings in water at room temperature. , 2011, The Journal of organic chemistry.

[22]  P. Herdewijn,et al.  Discovery of 7-N-piperazinylthiazolo[5,4-d]pyrimidine analogues as a novel class of immunosuppressive agents with in vivo biological activity. , 2011, Journal of medicinal chemistry.

[23]  John Blacker,et al.  Pharmaceutical process development : current chemical and engineering challenges , 2011 .

[24]  Y. Hashimoto,et al.  Synthesis and Antihepatitis C Virus Activity of Morpholino Triazine Derivatives. , 2010 .

[25]  Wei-hua Zhang,et al.  Synthesis of 3‐methyl‐N‐substituted‐1H‐indole , 2009 .

[26]  B. Lipshutz,et al.  Micellar catalysis of Suzuki-Miyaura cross-couplings with heteroaromatics in water. , 2008, Organic letters.

[27]  Q. Guo,et al.  Regioselective Pd-catalyzed indolization of 2-bromoanilines with internal alkynes using phosphine-free ligands , 2008 .

[28]  Roger A. Sheldon,et al.  The E Factor: fifteen years on , 2007 .

[29]  V. Chandregowda,et al.  Convergent Approach for Commercial Synthesis of Gefitinib and Erlotinib , 2007 .

[30]  B. Glasgow,et al.  ANS fluorescence: potential to augment the identification of the external binding sites of proteins. , 2007, Biochimica et biophysica acta.

[31]  E. Paetzold,et al.  Reactions in micellar systems. , 2005, Angewandte Chemie.

[32]  C. Deber,et al.  Interhelical Packing in Detergent Micelles , 2002, The Journal of Biological Chemistry.

[33]  M. Nakagawa,et al.  A concise synthesis of physostigmine from skatole and activated aziridine via alkylative cyclization. , 2000, Organic letters.

[34]  E. Kumazawa,et al.  Synthesis and antitumor activity of novel benzophenone derivatives. , 1997, Chemical & pharmaceutical bulletin.

[35]  M. Karelson,et al.  Prediction of Critical Micelle Concentration Using a Quantitative Structure−Property Relationship Approach. 1. Nonionic Surfactants , 1996 .

[36]  Stephen A. Smith,et al.  [[omega-(Heterocyclylamino)alkoxy]benzyl]-2,4-thiazolidinediones as potent antihyperglycemic agents. , 1994, Journal of medicinal chemistry.