Research graph
References from Iron-Catalyzed Selective Etherification and Transetherification Reactions Using Alcohols. Local targets link to admitted publications; unresolved targets remain external evidence.
A review on the advancement of ether synthesis from organic solvent to water
10.1039/c6ra12914e · 2016 · External reference
From Glycerol to Value-Added Products
10.1002/anie.200604694 · 2007 · External reference
Synthesis of methyl diantilis, a commercially important fragrance
10.1021/ed083p285 · 2006 · External reference
Ueber die Theorie der Aetherbildung
10.1002/jlac.18510770104 · 1851 · External reference
Unresolved reference
1996 · External reference
Unresolved reference
1979 · External reference
C–O cross-coupling of activated aryl and heteroaryl halides with aliphatic alcohols
10.1002/anie.201203460 · 2012 · External reference
Modern synthetic methods for copper-mediated C(aryl)–O, C(aryl)–N, and C(aryl)–S Bond Formation
10.1002/anie.200300594 · 2003 · External reference
Transition metal catalyzed synthesis of arylamines and aryl ethers from aryl halides and triflates: Scope and mechanism
10.1002/(sici)1521-3773(19980817)37:15<2046::aid-anie2046>3.0.co;2-l · 1998 · External reference
Mitsunobu and related reactions: Advances and applications
10.1021/cr800278z · 2009 · External reference
Copper/amino acid catalyzed cross-couplings of aryl and vinyl halides with nucleophiles
10.1021/ar8000298 · 2008 · External reference
The Mitsunobu reaction: Origin, mechanism, improvements, and applications
10.1002/asia.200700182 · 2007 · External reference
Renaissance of Ullmann and Goldberg reactions – progress in copper catalyzed C–N–, C–O– and C–S-coupling
10.1055/s-2003-42473 · 2003 · External reference
An efficient one-pot synthesis of unsymmetrical ethers: A directly reductive deoxygenation of esters using an InBr3/Et3SiH catalytic system
10.1021/jo070814z · 2007 · External reference
Efficient methods for the preparation of alkyl–aryl and symmetrical or unsymmetrical dialkyl ethers between alcohols and phenols or two alcohols by oxidation–reduction condensation
10.1021/ja0487877 · 2004 · External reference
Olefin hydroaryloxylation catalyzed by pincer–Iridium complexes
10.1021/ja404566v · 2013 · External reference
An efficient one-pot synthesis of unsymmetrical ethers: A directly reductive deoxygenation of esters using an InBr3/Et3SiH catalytic system
10.1021/jo070814z · 2007 · External reference
General ether synthesis under mild acid-free conditions. Trimethylsilyl iodide catalyzed reductive coupling of carbonyl compounds with trialkylsilanes to symmetrical ethers and reductive condensation with alkoxysilanes to unsymmetrical ethers
10.1021/jo00228a031 · 1987 · External reference
Copper-catalyzed etherification of arene C–H bonds
10.1021/ol402904d · 2013 · External reference
Pd(II)-catalyzed alkoxylation of unactivated C(sp3)–H and C(sp2)–H bonds using a removable directing group: Efficient synthesis of alkyl ethers
10.1039/c3sc51993g · 2013 · External reference
Efficient alkyl ether synthesis via palladium-catalyzed, picolinamide-directed alkoxylation of unactivated C(sp3)–H and C(sp2)–H bonds at remote positions
10.1021/ja3023972 · 2012 · External reference
Pd(OAc)2-catalyzed alkoxylation of arylnitriles via sp2 C–H bond activation using cyano as the directing group
10.1021/jo301384r · 2012 · External reference
Palladium-catalyzed ortho-alkoxylation of anilides via C–H activation
10.1021/jo301964m · 2012 · External reference
Pd(II)-catalyzed hydroxyl-directed C–H activation/C–O cyclization: Expedient construction of dihydrobenzofurans
10.1021/ja105366u · 2010 · External reference
Synthesis at the molecular frontier
10.1038/460197a · 2009 · External reference
On inventing reactions for atom economy
10.1021/ar010068z · 2002 · External reference
The atom economy─a search for synthetic efficiency
10.1126/science.1962206 · 1991 · External reference
Key green chemistry research areas─a perspective from pharmaceutical manufacturers
10.1039/b703488c · 2007 · External reference
Displacement by Substitution Process
10.1016/b0-08-045047-4/00136-9 · 2007 · External reference
Unresolved reference
1991 · External reference
Dehydration reactions in water. Brønsted acid-surfactant-combined catalyst for ester, ether, thioether, and dithioacetal formation in water
10.1021/ja026241j · 2002 · External reference
Industrial application of solid acid–base catalysts
10.1016/s0926-860x(98)00397-4 · 1999 · External reference
Niobium compounds: preparation, characterization, and application in heterogeneous catalysis
10.1021/cr9800208 · 1999 · External reference
Catalytic synthesis of methanol, higher alcohols and ethers
10.1016/s0920-5861(96)00190-3 · 1997 · External reference
Gold(I)-catalysed dehydrative formation of ethers from benzylic alcohols and phenols
10.1039/c5gc00684h · 2015 · External reference
Water compatible gold(III)-catalysed synthesis of unsymmetrical ethers from alcohols
10.1002/chem.200701134 · 2008 · External reference
Selective catalytic synthesis of unsymmetrical ethers from the dehydrative etherification of two different alcohols
10.1021/cs5012537 · 2014 · External reference
Palladium-catalyzed SN1 reactions of secondary benzylic alcohols: Etherification, amination, and thioetherification
10.1002/ejoc.200390185 · 2003 · External reference
A facile conversion of alcohols into p-methoxybenzyl ethers (PMB-ethers) using p-methoxybenzyl alcohol–Yb(OTf)3
10.1021/jo990563x · 1999 · External reference
Organic reactions catalyzed by methylrhenium trioxide: Dehydration, amination, and disproportionation of alcohols
10.1021/jo951613a · 1996 · External reference
Catalytic etherification of alcohols in Shilov system: C–O versus C–H bond activation
10.1016/j.molcata.2016.07.012 · 2017 · External reference
Organohalide-catalyzed dehydrative O-alkylation between alcohols: a facile etherification method for aliphatic ether synthesis
10.1039/c5gc00284b · 2015 · External reference
Iron catalysis in organic synthesis: A critical assessment of what it takes to make this base metal a multitasking champion
10.1021/acscentsci.6b00272 · 2016 · External reference
Iron-catalyzed cross etherification of alcohols to form unsymmetrical benzyl ethers
10.1016/j.mcat.2016.12.014 · 2017 · External reference
Direct and efficient synthesis of unsymmetrical ethers from alcohols catalyzed by Fe(HSO4)3 under solvent-free conditions
10.1007/s11164-015-2098-y · 2016 · External reference
Iron-catalyzed ferrocenylmethanol OH substitution by S, N, P, and C nucleophiles
10.1002/ejic.201300239 · 2013 · External reference
Iron(II) catalyzed dehydrative etherification of alcohols: A convenient route to ferrocenylmethanol-ethers
10.1039/c2ra20708g · 2012 · External reference
Iron(III)-catalyzed nucleophilic substitution of the hydroxy group in benzoin by alcohols
10.1055/s-0031-1289738 · 2012 · External reference
Iron-catalyzed solvent-free conversion of alcohols and phenols into diphenylmethyl (DPM) ethers
10.1016/s0040-4039(02)00890-0 · 2002 · External reference
Selective and efficient alcoholyses of allylic, secondary- and tertiary benzylic alcohols in the presence of iron
10.1016/s0040-4020(97)10350-7 · 1998 · External reference
Facile synthesis of symmetrical bis(benzhydryl)ethers using p-toluenesulfonyl chloride under solvent-free conditions
10.1186/2191-2858-3-1 · 2013 · External reference
Secondary benzylation using benzyl alcohols catalyzed by lanthanoid, scandium, and hafnium triflate
10.1021/jo034255h · 2003 · External reference
Iron-catalyzed stereospecific olefin synthesis by direct coupling of alcohols and alkenes with alcohols
10.1021/ol200372y · 2011 · External reference
Selectivity enhancement of silica-supported sulfonic acid catalysts in water by coating of ionic liquid
10.1021/ol071356j · 2007 · External reference
Sulfated tungstate as hydroxyl group activator for preparation of benzyl, including p-methoxybenzyl ethers of alcohols and phenols
10.1080/00397911.2016.1230218 · 2016 · External reference
Catalytic hydroalkoxylation of alkenes by Iron(III) catalyst
10.1016/j.tetlet.2010.11.036 · 2011 · External reference
Lanthanide(III) Triflate catalyzed thermal and microwave assisted synthesis of benzyl ethers from benzyl alcohols
10.1055/s-2004-836063 · 2005 · External reference
A mild and simple procedure for the reductive cleavage of acetals and ketals
10.1016/0040-4020(95)00055-d · 1995 · External reference
Improved procedure for the reductive acetylation of acyclic esters and a new synthesis of ethers
10.1021/jo9914521 · 2000 · External reference
A novel efficient method for the synthesis of substituted olefins; cross coupling of two different alcohols using NaHSO4/SiO2
10.1039/c3cc42746c · 2013 · External reference
