Related references
Note: Only part of the references are listed.Graphene-Supported Spinel CuFe2O4 Composites: Novel Adsorbents for Arsenic Removal in Aqueous Media
Duong Duc La et al.
SENSORS (2017)
Chemoselective N-acetylation of primary aliphatic amines promoted by pivalic or acetic acid using ethyl acetate as an acetyl donor
Tomoki Yoshida et al.
TETRAHEDRON LETTERS (2017)
Silica sulfuric acid-coated Fe3O4 nanoparticles as high reusable nanocatalyst for the oxidation of sulfides into sulfoxides, protection and deprotection of hydroxyl groups using HMDS and Ac2O
Amin Rostami et al.
JOURNAL OF SAUDI CHEMICAL SOCIETY (2017)
A rapid flow strategy for the oxidative cyanation of secondary and tertiary amines via C-H activation
Kidus Tadele et al.
SCIENTIFIC REPORTS (2017)
Preparation, characterization and application of RHA/TiO2 nanocomposites in the acetylation of alcohols, phenols and amines
Mohadeseh Seddighi et al.
COMPTES RENDUS CHIMIE (2016)
Preparation of polydopamine sulfamic acid-functionalized magnetic Fe3O4 nanoparticles with a core/shell nanostructure as heterogeneous and recyclable nanocatalysts for the acetylation of alcohols, phenols, amines and thiols under solvent-free conditions
Hojat Veisi et al.
GREEN CHEMISTRY (2016)
Selective acetylation of primary alcohols by ethyl acetate
Raju Singha et al.
TETRAHEDRON LETTERS (2016)
Selective N-acetylation of aromatic amines using acetonitrile as acylating agent
Ujwal Pratim Saikia et al.
TETRAHEDRON LETTERS (2016)
Magnetic graphitic carbon nitride: its application in the C-H activation of amines
Sanny Verma et al.
CHEMICAL COMMUNICATIONS (2015)
Efficient approach for the chemoselective acetylation of alcohols catalyzed by a novel metal oxide nanocatalyst CuO-ZnO
Jalal Albadi et al.
CHINESE JOURNAL OF CATALYSIS (2015)
Solventless acetylation of alcohols and phenols catalyzed by supported iron oxide nanoparticles
Fatemeh Rajabi et al.
CATALYSIS COMMUNICATIONS (2014)
Highly active magnetically separable CuFe2O4 nanocatalyst: an efficient catalyst for the green synthesis of tetrahydrofuro[3,4-b]quinoline-1,8(3H,4H) dione derivatives
Ramin Ghahremanzadeh et al.
JOURNAL OF THE IRANIAN CHEMICAL SOCIETY (2014)
Determination of the Cu 2p primary excitation spectra for Cu, Cu2O and CuO
N. Pauly et al.
SURFACE SCIENCE (2014)
Catalytic applications of a versatile magnetically separable Fe-Mo (Nanocat-Fe-Mo) nanocatalyst
Manoj B. Gawande et al.
GREEN CHEMISTRY (2013)
Magnetically recyclable magnetite-ceria (Nanocat-Fe-Ce) nanocatalyst - applications in multicomponent reactions under benign conditions
Manoj B. Gawande et al.
GREEN CHEMISTRY (2013)
Fundamentals of green chemistry: efficiency in reaction design
Roger A. Sheldon
CHEMICAL SOCIETY REVIEWS (2012)
Magnetically Recoverable Nanocatalysts
Vivek Polshettiwar et al.
CHEMICAL REVIEWS (2011)
POLY-(N,N′-DIBROMO-N-ETHYL-BENZENE-1,3-DISULFONAMIDE)AND N,N,N′,N′-TETRABROMOBENZENE-1,3-DISULFONAMIDE AS HIGHLY EFFICIENT CATALYSTS, AND (AC2O/SIO2) AS A HETEROGENEOUS SYSTEM FOR THE ACETYLATION OF ALCOHOLS, AMINES, AND THIOLS UNDER MICROWAVE IRRADIATION
Hojat Veisi et al.
PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS (2011)
Bismuth ferrite (BiFeO3) nanopowder prepared by sucrose-assisted combustion method: A novel and reusable heterogeneous catalyst for acetylation of amines, alcohols and phenols under solvent-free conditions
Saeid Farhadi et al.
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL (2009)
Indium triflate catalyzed peracetylation of carbohydrates
Nicholas P. Bizier et al.
CARBOHYDRATE RESEARCH (2008)
Widely useful DMAP-catalyzed esterification under auxiliary base- and solvent-free conditions
Akira Sakakura et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2007)
A novel 3-nitrobenzeneboronic acid as an extremely mild and einvironmentally benign catalyst for the acetylation of alcohols under solvent-free conditions
R. H. Tale et al.
TETRAHEDRON LETTERS (2006)
Molecular iodine in isopropenyl acetate (IPA): a highly efficient catalyst for the acetylation of alcohols, amines and phenols under solvent free conditions
Naseem Ahmed et al.
TETRAHEDRON LETTERS (2006)
A green protocol for chemoselective O-acylation in the presence of zinc oxide as a heterogeneous, reusable and eco-friendly catalyst
F Tamaddon et al.
TETRAHEDRON LETTERS (2005)
One-pot synthesis of per-O-acetylated thioglycosides from unprotected reducing sugars
G Agnihotri et al.
CARBOHYDRATE RESEARCH (2005)
Gadolinium triflate: an efficient and convenient catalyst for acetylation of alcohols and amines
R Alleti et al.
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL (2005)
Per-O-acetylation of sugars catalyzed by Ce(OTf)(3)
G Bartoli et al.
GREEN CHEMISTRY (2004)
Facile Cu(OTf)2-catalyzed preparation of per-O-acetylated hexopyranoses with stoichiometric acetic anhydride and sequential one-pot anomeric substitution to thioglycosides under solvent-free conditions
CA Tai et al.
JOURNAL OF ORGANIC CHEMISTRY (2003)
Lithium trifluoromethanesulfonate (LiOTf) as a recyclable catalyst for highly efficient acetylation of alcohols and diacetylation of aldehydes under mild and neutral reaction conditions
B Karimi et al.
JOURNAL OF ORGANIC CHEMISTRY (2003)
Perchloric acid adsorbed on silica gel as a new, highly efficient, and versatile catalyst for acetylation of phenols, thiols, alcohols, and amines
AK Chakraborti et al.
CHEMICAL COMMUNICATIONS (2003)
Sc(OTf)3-catalyzed acetolysis of 1,6-anhydro-β-hexopyranoses and solvent-free per-acetylation of hexoses
JC Lee et al.
TETRAHEDRON LETTERS (2002)
Catalytic acetylation of alcohols, phenols, thiols and amines with zeolite H-FER under solventless conditions
SP Chavan et al.
GREEN CHEMISTRY (2001)
Atom efficiency and catalysis in organic synthesis
RA Sheldon
PURE AND APPLIED CHEMISTRY (2000)