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    Highly chemoselective reductive amination-coupling by one-pot reaction of aldehydes, HMDS and NaBH4

    , Article Tetrahedron Letters ; Volume 49, Issue 47 , 2008 , Pages 6682-6684 ; 00404039 (ISSN) Azizi, N ; Akbari, E ; Khejeh Amiri, A ; Saidi, M. R ; Sharif University of Technology
    2008
    Abstract
    An efficient and highly chemoselective synthesis of symmetrical secondary amines via reductive amination of aldehydes with inexpensive and commercially available HMDS and sodium borohydride in high to quantitative yields is reported. © 2008 Elsevier Ltd. All rights reserved  

    A new and convenient approach to heterotetracyclic benzoxazocines through addition of 1,3-dicarbonyl compounds to quinolinium salts

    , Article Tetrahedron Letters ; Volume 51, Issue 20 , April , 2010 , Pages 2704-2707 ; 00404039 (ISSN) Matloubi Moghaddam, F ; Mirjafary, Z ; Saeidian, H ; Taheri, S ; Khodabakhshi, M. R ; Sharif University of Technology
    2010
    Abstract
    The synthesis of a series of benzoxazocines has been achieved in good yields by tandem C-alkylation and intramolecular O-alkylation of 1,3-dicarbonyl compounds with quinolinium salts. This is a novel example of the synthesis of eight-membered rings via a tandem process, which provides a method for the synthesis of medium-ring heterocycles  

    BF3·SiO2: an efficient reagent system for the one-pot synthesis of 1,2,4,5-tetrasubstituted imidazoles

    , Article Tetrahedron Letters ; Volume 49, Issue 16 , 2008 , Pages 2575-2577 ; 00404039 (ISSN) Sadeghi, B ; Mirjalili, B. B. F ; Hashemi, M. M ; Sharif University of Technology
    2008
    Abstract
    Silica-supported boron trifluoride (BF3·SiO2) is an efficient, readily available and reusable catalyst for the synthesis of 1,2,4,5-tetrasubstituted imidazoles using benzil, an aromatic aldehyde and an amine in the presence of ammonium acetate. This one-pot procedure is very simple, affording good to excellent yields. © 2008 Elsevier Ltd. All rights reserved  

    Sodium borohydride-solid LiClO4: An effective reagent for reducing aldehydes and ketones in aprotic solvent

    , Article Synthetic Communications ; Volume 35, Issue 17 , 2005 , Pages 2271-2276 ; 00397911 (ISSN) Halimjani, A. Z ; Saidi, M. R ; Sharif University of Technology
    2005
    Abstract
    An efficient and simple method for the reduction of aldehydes, ketones and acid chlorides has been accomplished by using NaBH4-solid LiClO 4 in mild conditions at ambient temperature with complete chemoselectivity in reduction of α,β-unsaturated aldehydes and ketones. The reaction is fast with high yield and simple workup. Copyright © Taylor & Francis, Inc  

    Pyridinium salts - Versatile reagents for the regioselective synthesis of functionalized thiazocino[2,3-b]indoles by tandem dinucleophilic reactions of thiooxindoles

    , Article Tetrahedron ; Volume 68, Issue 47 , 2012 , Pages 9685-9693 ; 00404020 (ISSN) Kiamehr, M ; Moghaddam, F. M ; Gormay, P. V ; Semeniuchenko, V ; Villinger, A ; Langer, P ; Iaroshenko, V. O ; Sharif University of Technology
    2012
    Abstract
    The reaction of thiooxindoles with various 2- and 3-substituted pyridinium salts afforded a variety of functionalized thiazocinoindoles. The products have been prepared in good to excellent yields by regioselective dinucleophilic C/S-cyclocondensation of thiooxindoles with pyridinium salts  

    The role of mscl amphipathic n terminus indicates a blueprint for bilayer-mediated gating of mechanosensitive channels

    , Article Nature Communications ; Volume 7 , 2016 ; 20411723 (ISSN) Bavi, N ; Cortes, D. M ; Cox, C. D ; Rohde, P. R ; Liu, W ; Deitmer, J. W ; Bavi, O ; Strop, P ; Hill, A. P ; Rees, D ; Corry, B ; Perozo, E ; Martinac, B ; Sharif University of Technology
    Nature Publishing Group  2016
    Abstract
    The bacterial mechanosensitive channel MscL gates in response to membrane tension as a result of mechanical force transmitted directly to the channel from the lipid bilayer. MscL represents an excellent model system to study the basic biophysical principles of mechanosensory transduction. However, understanding of the essential structural components that transduce bilayer tension into channel gating remains incomplete. Here using multiple experimental and computational approaches, we demonstrate that the amphipathic N-terminal helix of MscL acts as a crucial structural element during tension-induced gating, both stabilizing the closed state and coupling the channel to the membrane. We... 

    Curcumin as a green fluorescent label to revive the fluorescence property of functionalized graphene oxide nanosheets

    , Article Journal of Drug Delivery Science and Technology ; Volume 45 , June , 2018 , Pages 422-427 ; 17732247 (ISSN) Akbari, E ; Akhavan, O ; Hatamie, S ; Rahighi, R ; Sharif University of Technology
    Editions de Sante  2018
    Abstract
    In this work, graphene oxide (GO) aqueous suspensions prepared by a chemical exfoliation method showed a fluorescence peak at ∼615 nm. Photoluminescence spectroscopy determined that functionalization of the GO sheets by 3-(2-Aminoethylamino) propyltrimethoxysilane molecules significantly quench the fluorescence property of the GO sheets. Fourier transform infrared spectroscopy confirmed proper functionalization of the GO sheets. Curcumin was applied as a fluorescent natural material with an emission peak at ∼550 nm wavelength for green fluorescent labeling of the functionalized-GO sheets. The curcumin-labeled functionalized-GO sheets showed an intense emission band fluorescent property with... 

    A simple and novel eco-friendly process for the synthesis of cyclic dithiocarbonates from epoxides and carbon disulfide in water

    , Article Journal of Heterocyclic Chemistry ; Volume 46, Issue 2 , 2009 , Pages 347-350 ; 0022152X (ISSN) Ziyaei Halimehjani, A ; Ebrahimi, F ; Azizi, N ; Saidi, M. R ; Sharif University of Technology
    2009
    Abstract
    The reaction of oxiranes with carbon disulfide for preparation of cyclic dithiocarbonates was carried out in water under catalytic amount of an organic base such as dimethylaminopyridine or triethylamine. The reaction conditions are simple and give high yields of desired products.© 2009 HeteroCorporation  

    Regiospecific iodocyclization of S-allyl dithiocarbamates: synthesis of 2-imino-1,3-dithiolane and 2-iminium-1,3-dithiolane derivatives

    , Article Tetrahedron Letters ; Volume 50, Issue 23 , 2009 , Pages 2747-2749 ; 00404039 (ISSN) Ziyaei Halimehjani, A ; Maleki, H ; Saidi, M. R ; Sharif University of Technology
    2009
    Abstract
    4-Alkyl-2-imino-1,3-dithiolanes and 4-alkyl-2-iminium-1,3-dithiolanes were prepared in excellent yields with complete regiospecificity under mild conditions by the iodocyclization of S-allyl dithiocarbamates. Dehydrohalogenation of the 4-alkyl-2-imino-1,3-dithiolanes gave 4-alkylidene-2-imino-1,3-dithiolanes in excellent yields. © 2009 Elsevier Ltd. All rights reserved  

    Synthesis of aza-Henry products and enamines in water by Michael addition of amines or thiols to activated unsaturated compounds

    , Article Tetrahedron Letters ; Volume 49, Issue 7 , 2008 , Pages 1244-1248 ; 00404039 (ISSN) Ziyaei Halimehjani, A ; Saidi, M. R ; Sharif University of Technology
    2008
    Abstract
    Nitroamines and nitrothiols were synthesized in high yields by the Michael addition of amines and thiols to nitroolefins without using any catalyst. Also, the reaction of amines with dimethylacetylene dicarboxylate (DMAD) in water afforded the corresponding enamines. © 2007 Elsevier Ltd. All rights reserved  

    LiClO4-accelerated three-component Mannich-type reaction of diethyl malonate with imines: An efficient synthesis of β-amino esters under solvent-free conditions

    , Article Synthetic Communications ; Volume 38, Issue 22 , 2008 , Pages 4036-4044 ; 00397911 (ISSN) Aryanasab, F ; Saidi, M. R ; Sharif University of Technology
    2008
    Abstract
    LiClO4 is used as catalyst for direct Mannich-type reaction of aryl aldehydes, aryl amines, and diethyl malonic ester under solvent-free conditions. This three-component reaction afforded the corresponding β-amino esters in good yields with simple and environmentally benign procedure. Copyright © Taylor & Francis Group, LLC  

    ZrOCl2·8H2O on montmorillonite K10 accelerated conjugate addition of amines to α,β-unsaturated alkenes under solvent-free conditions

    , Article Tetrahedron ; Volume 62, Issue 4 , 2006 , Pages 672-677 ; 00404020 (ISSN) Hashemi, M. M ; Eftekhari-Sis, B ; Abdollahifar, A ; Khalili, B ; Sharif University of Technology
    2006
    Abstract
    At room temperature, ZrOCl2·8H2O on montmorillonite K10 efficiently catalyzes conjugate addition of amines to a variety of conjugated alkenes such as α,β-unsaturated carbonyl compounds, carboxylic esters, nitriles and amides under solvent-free conditions. The catalyst can be recycled for subsequent reactions without any appreciable loss of efficiency. © 2005 Elsevier Ltd. All rights reserved  

    Highly efficient synthesis of pyrimido[4,5-d]pyrimidine-2,4-dione derivatives catalyzed by iodine

    , Article Tetrahedron Letters ; 2014 , p. 4720-4723 Moghaddam, F. M ; Khodabakhshi, M. R ; Aminaee, M ; Sharif University of Technology
    Abstract
    A new and efficient synthesis of pyrimido[4,5-d]pyrimidine-2,4-dione derivatives through the reaction of 6-aminouracils and N,N′-bis(arylmethylidene) arylmethane in the presence of molecular iodine as a readily available and feasible catalyst  

    A one-pot, three-component regiospecific synthesis of dispiropyrrolidines containing a thiophenone ring via 1,3-dipolar cycloaddition reactions of azomethine ylides

    , Article Tetrahedron Letters ; Volume 54, Issue 20 , May , 2013 , Pages 2520-2524 ; 00404039 (ISSN) Moghaddam, F. M ; Khodabakhshi, M. R ; Ghahremannejad, Z ; Foroushani, B. K ; Ng, S. W ; Sharif University of Technology
    2013
    Abstract
    The synthesis of new dispiropyrrolidines containing a thiophenone ring has been achieved by a one-pot, three-component 1,3-dipolar cycloaddition reaction. Unsaturated thiophenone dipolarophiles were reacted with azomethine ylides, generated in situ from sarcosine and cycloketone derivatives (isatin, ninhydrin, acenaphthoquinone), to produce the corresponding cycloadducts in good yields (70-90%). The cycloaddition reaction was found to be highly regio- and diastereoselective  

    Comments on the " A comparative study of chelating and cationic ion exchange resins for the removal of palladium (II) complexes from acidic chloride media"

    , Article Journal of Hazardous Materials ; Volume 229-230 , 2012 , Pages 461-462 ; 03043894 (ISSN) Alahyari, S. A ; Khanchi, A. R ; Outokesh, M ; Tayebi, A ; Sharif University of Technology

    Copper(II) acetate

    , Article Synlett ; Volume 23, Issue 13 , 2012 , Pages 1995-1996 ; 09365214 (ISSN) Amini, M ; Sharif University of Technology
    2012
    Abstract
    (A) Chakraborty and co-workers have developed a green method for the bulk ring-opening polymerization of lactides in the presence of Cu(OAc)2 as a good catalyst to synthesize polymers with different end-terminal groups.3 These polymerizations are highly controlled leading to the formation of polymers with the expected number of average molecular weights and narrow molecular weight distribution. (B) Garden and co-workers have found that the oxidative addition of anilines with 1,4-naphthoquinone to give N-aryl-2-amino-1,4-naphthoquinones can be performed in the presence of catalytic amounts of copper(II) acetate.4 All the reactions are generally more efficient in that they are cleaner, higher... 

    Surface modification for titanium implants by hydroxyapatite nanocomposite

    , Article Caspian Journal of Internal Medicine ; Volume 3, Issue 3 , 2012 , Pages 460-465 ; 20086164 (ISSN) Family, R ; Solati Hashjin, M ; Nik, S. N ; Nemati, A ; Sharif University of Technology
    2012
    Abstract
    Background: Titanium (Ti) implants are commonly coated with hydroxyapatite (HA). However, HA has some disadvantages such as brittleness, low tensile strength and fracture toughness. It is desirable to combine the excellent mechanical properties of ZrO 2 and the chemical inertness of Al 2O 3 with respect to the purpose of this project which was coating Ti implants with HA-ZrO 2-Al 2O 3 to modify the surface of these implants by adding ZrO 2 and Al 2O 3 to HA. The purpose of this study was to evaluate the efficacy of hydroxyapatite coating nonocomposite. Methods: From September 2009 to January2011, functionally graded HA-Al 2O 3-ZrO 2 and HA coatings were applied on Ti samples. HA-Al 2O 3-ZrO... 

    A facile synthesis of bridged polycyclic naphthooxazocine skeletons: Eight-membered-ring constructions via tandem dinucleophilic addition of naphthalenols to quinolinium salts

    , Article Helvetica Chimica Acta ; Volume 94, Issue 1 , 2011 , Pages 142-147 ; 0018019X (ISSN) Matloubi Moghaddam, F ; Taheri, S ; Mirjafary, Z ; Saeidian, H ; Kiamehr, M ; Tafazzoli, M ; Sharif University of Technology
    2011
    Abstract
    The efficient synthesis of bridged polycyclic naphthooxazocines 3 via addition of naphthalenols 1 as a bis-nucleophile to N-alkylquinolinium salts 2 is described (Scheme 1 and Table 2). This new approach provides a powerful entry into polycyclic structures containing bicyclic N,O-acetals related to bioactive compounds  

    Nanocrystalline copper(II) oxide-catalyzed one-pot synthesis of imidazo[1,2-a]quinoline and quinolino[1,2-a]quinazoline derivatives via a three-component condensation

    , Article Synthetic Communications ; Volume 41, Issue 3 , Jan , 2011 , Pages 426-435 ; 00397911 (ISSN) Ahmadi, S. J ; Hosseinpour, M ; Sadjadi, S ; Sharif University of Technology
    2011
    Abstract
    A simple, efficient, and practical procedure for the synthesis of imidazo[1,2-a]quinoline and quinolino[1,2-a]quinazoline derivatives using CuO nanoparticles as a novel catalyst in excellent yields is described. The catalyst can be recovered conveniently and reused at least four times without any loss of activity  

    A simple and efficient total synthesis of (±)-danshexinkun A, a bioactive diterpenoid from Salvia miltiorrhiza

    , Article Tetrahedron Letters ; Volume 51, Issue 3 , 2010 , Pages 540-542 ; 00404039 (ISSN) Matloubi Moghaddam, F ; Moridi Farimani, M ; Sharif University of Technology
    Abstract
    An efficient 12-step route for the synthesis of the diterpenoid quinone (±)-danshexinkun A in 23% overall yield from the corresponding highly substituted stilbene using a photocyclization strategy is described