Related references
Note: Only part of the references are listed.Tunable aryl imidazolium ionic liquids (TAIILs) as environmentally benign catalysts for the esterification of fatty acids to biodiesel fuel
Mayur Thul et al.
CATALYSIS COMMUNICATIONS (2021)
Development of a Novel Method for Trimethylsilylation of Saccharides
Jyun-Siao Chen et al.
SYNTHESIS-STUTTGART (2021)
Tunable Aryl Imidazolium Recyclable Ionic Liquid with Dual BrOnsted-Lewis Acid as Green Catalyst for Friedel-Crafts Acylation and Thioesterification
Yi-Jyun Lin et al.
MOLECULES (2020)
Reusable Bronsted Acidic Ionic Liquid Efficiently Catalyzed N-Formylation and N-Acylation of Amines
Chun Li et al.
ACS SUSTAINABLE CHEMISTRY & ENGINEERING (2020)
Ionic Liquid Catalyzed Per-O-Acetylation and Benzylidene Ring-Opening Reaction
Mayur Thul et al.
CATALYSTS (2020)
Synthesis of task-specific imidazolium ionic liquid as an efficient catalyst in acetylation of alcohols, phenols, and amines
Snehkrishn A. Chaubey et al.
CHEMICAL PAPERS (2020)
A simple and efficient room temperature silylation of diverse functional groups with hexamethyldisilazane using CeO2 nanoparticles as solid catalysts
Nagaraj Anbu et al.
MOLECULAR CATALYSIS (2019)
Room temperature silylation of alcohols catalyzed by metal organic frameworks
Amarajothi Dhakshinamoorthy et al.
CATALYSIS SCIENCE & TECHNOLOGY (2017)
Chlorozincate(II) acidic ionic liquid: Efficient and biodegradable silylation catalyst
Faezeh Abbasi et al.
APPLIED ORGANOMETALLIC CHEMISTRY (2017)
Highly efficient protection of alcohols and phenols catalysed by tin porphyrin supported on MIL-101
Farnaz Zadehahmadi et al.
APPLIED ORGANOMETALLIC CHEMISTRY (2015)
Chemoselective per-O-trimethylsilylation and homogeneous N-functionalisation of amino sugars
A. Abragam Joseph et al.
CHEMICAL COMMUNICATIONS (2015)
Microwave-Assisted One-Pot Synthesis of 1,6-Anhydrosugars and Orthogonally Protected Thioglycosides
Yen-Chun Ko et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2014)
Lewis basic ionic liquid as an efficient and facile catalyst for acetylation of alcohols, phenols, and amines under solvent-free conditions
Li Ji et al.
MONATSHEFTE FUR CHEMIE (2013)
Nanocrystalline TiO2-HCIO4 as a new, efficient and recyclable catalyst for the chemoselective trimethylsilylation of alcohols, phenols and deprotection of silyl ethers
Farhad Shirini et al.
CATALYSIS COMMUNICATIONS (2012)
Preparation, characterization and use of 1,3-disulfonic acid imidazolium hydrogen sulfate as an efficient, halogen-free and reusable ionic liquid catalyst for the trimethylsilyl protection of hydroxyl groups and deprotection of the obtained trimethylsilanes
Farhad Shirini et al.
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL (2012)
Synthesis of α-germyl and α-silylcarboxylic acids and selected electrochemical oxidations
Anna Rakovshik et al.
JOURNAL OF ORGANOMETALLIC CHEMISTRY (2012)
Highly efficient and selective trimethylsilylation of alcohols and phenols with hexamethyldisilazane catalyzed by polystyrene-bound tin(IV) porphyrin
Shadab Gharaati et al.
POLYHEDRON (2012)
An efficient synthesis of silyl ethers of primary alcohols, secondary alcohols, phenols and oximes with a hydrosilane using InBr3 as a catalyst
Madabhushi Sridhar et al.
TETRAHEDRON LETTERS (2011)
An efficient catalytic route for the preparation of silyl ethers using alumina-supported heteropolyoxometalates
Paula Villabrille et al.
APPLIED CATALYSIS B-ENVIRONMENTAL (2010)
Tunable Aryl Alkyl Ionic Liquids (TAAILs): The Next Generation of Ionic Liquids
Sebastian Ahrens et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2009)
Highly regio- and chemoselective silylation of diethyl α-hydroxyphosphonates, alcohols and phenols in the presence of solid TiCl3(OTf) as a catalyst with hexamethyldisilazane (HMDS) at room temperature in the absence of solvent
Habib Firouzabadi et al.
CATALYSIS COMMUNICATIONS (2009)
Rapid and highly efficient trimethylsilylation of alcohols and phenols with hexamethyldisilazane (HMDS) catalyzed by reusable zirconyl triflate, [ZrO(OTf)2]
Majid Moghadam et al.
JOURNAL OF ORGANOMETALLIC CHEMISTRY (2008)
An imidazolium tosylate salt as efficient and recyclable catalyst for acetylation in an ionic liquid
Ye Liu et al.
MONATSHEFTE FUR CHEMIE (2008)
Efficient trimethylsilylation of alcohols and phenols in the presence of ZrCl4 as a reusable catalyst
Farhad Shirini et al.
CATALYSIS COMMUNICATIONS (2007)
Efficient and practical protocol for silylation of hydroxyl groups using reusable lithium perchlorate dispersed in silica gel under neutral condition
N Azizi et al.
JOURNAL OF ORGANOMETALLIC CHEMISTRY (2006)
Two-carbon homologation of ketones via silylketene acetals:: Synthesis of α,β-unsaturated acids and α-trimethylsilyl δ-ketoacids
M Bellassoued et al.
JOURNAL OF ORGANOMETALLIC CHEMISTRY (2005)
Protection (and deprotection) of functional groups in organic synthesis by heterogeneous catalysis
G Sartori et al.
CHEMICAL REVIEWS (2004)
Metallic Lewis acids-catalyzed acetylation of alcohols with acetic anhydride and acetic acid in ionic liquids: study on reactivity and reusability of the catalysts
SG Lee et al.
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL (2003)
Novel bronsted acidic ionic liquids and their use as dual solvent-catalysts
AC Cole et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2002)
Tungstophosphoric acid (H3PW12O40) as a heterogeneous inorganic catalyst. Activation of hexamethyldisilazane (HMDS) by tungstophosphoric acid for efficient and selective solvent-free O-silylation reactions
H Firouzabadi et al.
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 (2002)
Mild and highly efficient method for the silylation of alcohols using hexamethyldisilazane catalyzed by iodine under nearly neutral reaction conditions
B Karimi et al.
JOURNAL OF ORGANIC CHEMISTRY (2000)