Trityl chloride as an efficient organic catalyst for the synthesis of 1-amidoalkyl-2-naphtols in neutral media at room temperature
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[1] Maneesh K. Gupta,et al. An efficient organocatalyzed multicomponent synthesis of diarylmethanes via Mannich type Friedel–Crafts reaction , 2009 .
[2] J. Pandey,et al. L-Proline catalyzed multicomponent reaction of 3,4-dihydro-(2H)-pyran, urea/thiourea, and aldehydes: diastereoselective synthesis of hexahydropyrano pyrimidinones (thiones) , 2009 .
[3] P. T. Perumal,et al. Synthesis of highly functionalized oxazines by Vilsmeier cyclization of amidoalkyl naphthols , 2009 .
[4] S. Chandrasekhar,et al. Proline-threonine dipeptide as an organocatalyst for the direct asymmetric aldol reaction , 2009 .
[5] M. Naimi-Jamal,et al. An expeditious synthesis of cyanohydrin trimethylsilyl ethers using tetraethylammonium 2-(carbamoyl)benzoate as a bifunctional organocatalyst , 2009 .
[6] K. Saidi,et al. Heteropoly acid catalyzed synthesis of 1-amidoalkyl-2-naphthols in the presence of molten tetraethyl ammonium chloride as an ionic liquid , 2009 .
[7] A. Shirazi,et al. Triarylmethyl chlorides as novel, efficient, and mild organic catalysts for the synthesis of N-sulfonyl imines under neutral conditions , 2008 .
[8] H. Shaterian,et al. A modified reaction for the preparation of amidoalkyl naphthols , 2008 .
[9] H. Shaterian,et al. Silica supported perchloric acid (HClO4–SiO2): an efficient and recyclable heterogeneous catalyst for the one-pot synthesis of amidoalkyl naphthols , 2008 .
[10] A. Khalafi‐Nezhad,et al. Trityl Chloride as a Novel and Efficient Organic Catalyst For Room Temperature Preparation of Bis(indolyl)methanes under Solvent-Free Conditions in Neutral Media , 2008 .
[11] H. Shaterian,et al. Sodium hydrogen sulfate as effective and reusable heterogeneous catalyst for the one-pot preparation of amidoalkyl naphthols , 2008 .
[12] H. Shaterian,et al. An efficient, simple and expedition synthesis of 1-amidoalkyl-2-naphthols as 'drug like' molecules for biological screening. , 2008, Bioorganic & medicinal chemistry letters.
[13] B. Das,et al. An Improved Synthesis of Amidoalkyl Phenols Involving a Ritter-Type Reaction , 2007 .
[14] S. Kantevari,et al. Potassium dodecatungstocobaltate trihydrate (K5CoW12O40 · 3H2O): A mild and efficient reusable catalyst for the synthesis of amidoalkyl naphthols in solution and under solvent-free conditions , 2007 .
[15] S. D. Samant,et al. Ultrasound-promoted synthesis of 1-amidoalkyl-2-naphthols via a three-component condensation of 2-naphthol, ureas/amides, and aldehydes, catalyzed by sulfamic acid under ambient conditions. , 2007, Ultrasonics sonochemistry.
[16] S. D. Samant,et al. Cation‐Exchanged Resins: Efficient Heterogeneous Catalysts for Facile Synthesis of 1‐Amidoalkyl‐2‐naphthols from One‐Pot, Three‐Component Condensations of Amides/Ureas, Aldehydes, and 2‐Naphthol , 2007 .
[17] B. Das,et al. Iodine catalyzed preparation of amidoalkyl naphthols in solution and under solvent-free conditions ☆ , 2007 .
[18] P. T. Perumal,et al. A new synthesis of acetamido phenols promoted by Ce(SO4)2 , 2006 .
[19] A. Khosropour,et al. A simple and efficient procedure for the synthesis of amidoalkyl naphthols by p-TSA in solution or under solvent-free conditions , 2006 .
[20] D. Steinhilber,et al. Molecular biology in medicinal chemistry , 2004 .
[21] V. Yardley,et al. Design, synthesis, and biological evaluation of a series of simple and novel potential antimalarial compounds. , 2001, Bioorganic & medicinal chemistry letters.
[22] C. L. Chen,et al. Synthesis and cardiovascular evaluation of N-substituted 1-aminomethyl-2-naphthols , 1999 .
[23] S. Kusumoto,et al. BENZYL TRITYL ETHER AND DDQ AS NEW TRITYLATING REAGENTS , 1998 .
[24] T. Kuroki,et al. Antirheumatic agents: novel methotrexate derivatives bearing a benzoxazine or benzothiazine moiety. , 1997, Journal of medicinal chemistry.
[25] M. Millan,et al. Tetracyclic analogues of [+]-S 14297: Synthesis and determination of affinity and selectivity at cloned human dopamine D3 vs D2 receptors , 1997 .
[26] G. Gromo,et al. New antianginal nitro esters with reduced hypotensive activity. Synthesis and pharmacological evaluation of 3-[(nitrooxy)alkyl]-2H-1,3-benzoxazin-4(3H)-ones. , 1995, Journal of medicinal chemistry.
[27] Ch'en Cl,et al. Electrophysiological basis for the bradycardic effects of 1-(1-pyrrolidinylmethyl)-2-naphthol in rodents. , 1992 .
[28] T. Mukaiyama,et al. New role of tin(II) compounds in organic synthesis , 1990 .
[29] A. Kluge,et al. Synthesis and antihypertensive activity of 4'-substituted spiro[4H-3,1-benzoxazine-4,4'-piperidin]-2(1H)-ones. , 1983, Journal of medicinal chemistry.
[30] T. Ōishi. Protective Group in Organic Synthesis , 1978 .
[31] G A Howie,et al. Antimitotic activity of the potent tumor inhibitor maytansine. , 1975, Science.
[32] Peter Y. Johnson,et al. The synthesis and antitumor properties of a 6-Alkoxy tetrahydrooxazine , 1973 .
[33] M. Wani,et al. Plant antitumour agents: colubrinol acetate and colubrinol, antileukaemic ansa macrolides from Colubrina texensis , 1973 .
[34] S. Esumi,et al. The structure of minimycin, a novel carbon-linked nucleoside antibiotic related to -pseudouridine. , 1972, The Journal of antibiotics.
[35] O. Kawaguchi,et al. Minimycin, a new antibiotic. , 1972, The Journal of antibiotics.
[36] T. Okazaki,et al. Oxazinomycin, a new carbon-linked nucleoside antibiotic. , 1971, The Journal of antibiotics.
[37] G. Y. Lesher,et al. A New Method for the Preparation of 3-Substituted-2-oxazolidones , 1955 .
[38] H. Mosher,et al. Heterocyclic Diphenylmethane Derivatives , 1953 .