Related references
Note: Only part of the references are listed.Chemistry and glycobiology
Chung-Yi Wu et al.
CHEMICAL COMMUNICATIONS (2011)
Iron(III) chloride-tandem catalysis for a one-pot regioselective protection of glycopyranosides
Yann Bourdreux et al.
CHEMICAL COMMUNICATIONS (2011)
Regioselective One-pot Protection and Protection-glycosylation of Carbohydrates
Cheng-Chung Wang et al.
CHIMIA (2011)
Synthesis of Maradolipid
Vikram A. Sarpe et al.
JOURNAL OF ORGANIC CHEMISTRY (2011)
Synthesis of 3-O-sulfonated heparan sulfate octasaccharides that inhibit the herpes simplex virus type 1 host-cell interaction
Yu-Peng Hu et al.
NATURE CHEMISTRY (2011)
One-Pot Strategies for the Synthesis of the Tetrasaccharide Linkage Region of Proteoglycans
Teng-Yi Huang et al.
ORGANIC LETTERS (2011)
Glycomics Hits the Big Time
Gerald W. Hart et al.
CELL (2010)
Recent Trends in Regioselective Protection and Deprotection of Monosaccharides
Marco Filice et al.
CURRENT ORGANIC CHEMISTRY (2010)
Catalyst-free silylation of alcohols and phenols by promoting HMDS in CH3NO2 as solvent
Santosh T. Kadam et al.
GREEN CHEMISTRY (2010)
H5IO6/KI: A New Combination Reagent for Iodination of Aromatic Amines, and Trimethylsilylation of Alcohols and Phenols through in situ Generation of Iodine under Mild Conditions
Mohammad Ali Zolfigol et al.
HELVETICA CHIMICA ACTA (2010)
The promise of glycomics, glycan arrays and carbohydrate-based vaccines
Bernd Lepenies et al.
IMMUNOPHARMACOLOGY AND IMMUNOTOXICOLOGY (2010)
One-Pot Syntheses of Immunostimulatory Glyeolipids
Matthew Schombs et al.
JOURNAL OF ORGANIC CHEMISTRY (2010)
Regioselective One-Pot Protection of D-Glucosamine
Ken-Lien Chang et al.
JOURNAL OF ORGANIC CHEMISTRY (2010)
Selective Acetylation of per-O-TMS-Protected Monosaccharides
Mark A. Witschi et al.
ORGANIC LETTERS (2010)
The first unique synthetic mycobacterial cord factors
Juma'a R. Al Dulayymi et al.
TETRAHEDRON LETTERS (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)
Regioselective one-pot protection of glucose
Cheng-Chung Wang et al.
NATURE PROTOCOLS (2008)
Two-Step Synthesis of the Immunogenic Bacterial Glycolipid BbGL1
Suvarn S. Kulkarni et al.
ORGANIC LETTERS (2008)
Lanthanum trichloride: An efficient catalyst for the silylation of hydroxyl groups by activating hexamethyldisilazane (HMDS)
Akkirala Venkat Narsaiah
JOURNAL OF ORGANOMETALLIC CHEMISTRY (2007)
1,3-Dibromo-5,5-diethylbarbituric acid as an efficient catalyst for the protection of various alcohols with HMDS under solvent-free conditions
Ardeshir Khazaei et al.
CATALYSIS COMMUNICATIONS (2007)
Synthesis and medical applications of oligosaccharides
Peter H. Seeberger et al.
NATURE (2007)
Regioselective one-pot protection of carbohydrates
Cheng-Chung Wang et al.
NATURE (2007)
Trichloroisocyanuric acid (TCCA) as a mild and efficient catalyst for the trimethylsilylation of alcohols and phenols with hexamethyldisilazane (HMDS) under heterogonous conditions
Ardeshir Khazaei et al.
CATALYSIS COMMUNICATIONS (2007)
A novel and highly efficient method for the silylation of alcohols with hexamethyldisilazane (HMDS) catalyzed by recyclable sulfonic acid-functionalized ordered nanoporous silica
Daryoush Zareyee et al.
TETRAHEDRON LETTERS (2007)
Efficient, one-pot syntheses of biologically active alpha-linked glycolipids
Wenjun Du et al.
CHEMICAL COMMUNICATIONS (2007)
Indium tribromide: An efficient catalyst for the silylation of hydroxy groups by the activation of hexamethyldisilazane
J. S. Yadav et al.
SYNTHESIS-STUTTGART (2006)
Poly(N-bromobenzene-1,3-disulfonamide) and N,N,N′,N′-tetrabromobenzene-1,3-disulfonamide as novel catalytic reagents for silylation of alcohols, phenols, and thiols using hexamethyldisilazane
Ramin Ghorbani-Vaghei et al.
TETRAHEDRON LETTERS (2006)
Efficient synthesis of α-galactosyl ceramide analogues using glycosyl iodide donors
WJ Du et al.
ORGANIC LETTERS (2005)
Novel and efficient method for the silylation of hydroxyl groups with hexamethyldisilazane (HMDS) under solvent-free and neutral conditions
N Azizi et al.
ORGANOMETALLICS (2004)
Cu(OTf)2-catalyzed Et3SiH-reductive etherification of various carbonyl compounds with trimethylsilyl ethers
WC Yang et al.
TETRAHEDRON LETTERS (2003)
Copper triflate [Cu(OTf)2] is an efficient and mild catalyst for the silylation of α-hydroxyphosphonates to α-trimethylsilyloxyphosphonates with HMDS at room temperature
H Firouzabadi et al.
TETRAHEDRON LETTERS (2003)
A high yielding preparation of α-trimethylsilyloxyphosphonates by silylation of α-hydroxyphosphonates with HMDS catalyzed by iodine
H Firouzabadi et al.
TETRAHEDRON LETTERS (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)
Efficient syntheses of β-cyanosugars using glycosyl iodides derived from per-O-silylated mono- and disaccharides
AS Bhat et al.
ORGANIC LETTERS (2001)
Automated solid-phase synthesis of oligosaccharides
OJ Plante et al.
SCIENCE (2001)
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)