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Synthesis and application of novel carbohydrate-based ammonium and triazolium salts
1 of 49 checkable references need attention · checked 2026-07-23
At the dated check, the references listed below either did not resolve in Crossref or DataCite, or carried a retraction notice. Each one is shown with the registry record that put it there.
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References needing attention
does not resolve to a known work10.1002/1521-3773(20010601)40:11 < 2004::AID-ANIE2004 > 3.0.CO;2-5
The 48 checked references that resolve
resolves10.3762/bjoc.13.170
Chiral phase-transfer catalysis in the asymmetric α-heterofunctionalization of prochiral nucleophiles
resolves10.1021/ja1102844
Chiral 1,2,3-Triazoliums as New Cationic Organic Catalysts with Anion-Recognition Ability: Application to Asymmetric Alkylation of Oxindoles
resolves10.1039/c2cc32398b
Catalytic asymmetric Mannich-type reactions of α-cyano α-sulfonyl carbanions
resolves10.1021/ja411647x
Asymmetric Substitution at the Tetrasubstituted Chiral Carbon: Catalytic Ring-Opening Alkylation of Racemic 2,2-Disubstituted Aziridines with 3-Substituted Oxindoles
resolves10.1246/cl.150581
Catalytic Asymmetric Cyanation of Alkylideneindolenines Generated from Sulfonylalkylindoles
resolves10.1002/anie.199303361
Carbohydrates as Chiral Auxiliaries in Stereoselective Synthesis. New Synthetic Methods (90)
resolves10.1055/s-0030-1260143
More Than Just Sweet - Sugar-Derived Stereodifferentiating Agents for Asymmetric Synthesis
resolves10.1002/ejoc.201402689
Applications of Carbohydrate‐Based Organocatalysts in Enantioselective Synthesis
resolves10.2174/138527212799499877
The Enantiomeric Differentiation Ability of Chiral Crown Ethers Based on Carbohydrates
resolves10.1016/j.tetasy.2013.12.007
Enantioselective Michael addition of malonates to aromatic nitroalkenes catalyzed by monosaccharide-based chiral crown ethers
resolves10.1002/chir.22678
Synthesis of <scp>l</scp>‐threitol‐based crown ethers and their application as enantioselective phase transfer catalyst in Michael additions
resolves10.1039/C6NJ02030E
Synthesis of α-
<scp>d</scp>
-galactose-based azacrown ethers and their application as enantioselective catalysts in Michael reactions
resolves10.1016/j.tet.2018.04.087
Asymmetric cyclopropanation reactions catalyzed by carbohydrate-based crown ethers
resolves10.2174/157017912798889143
Chiral Ionic Liquids Derived from (-)-Ephedrine and Carbohydrates: Synthesis,Properties and Applications to Asymmetric Synthesis and Catalysis
resolves10.1021/ol071390y
Synthesis and Applications of Novel Bis(ammonium) Chiral Ionic Liquids Derived from Isomannide
resolves10.1016/j.tetasy.2008.02.009
Novel carbohydrate-based chiral ammonium ionic liquids derived from isomannide
resolves10.1039/C6RA02792J
A remarkable chiral recognition of racemic Mosher's acid salt by naturally derived chiral ionic liquids using
<sup>19</sup>
F NMR spectroscopy
resolves10.2174/157017807780737219
Synthesis of Novel Chiral Ammonium-Based Ionic Liquids Derived from Isosorbide and their Applications in an Asymmetric Aza Diels-Alder Reaction
resolves10.1039/b615650a
Glucose-derived ionic liquids: exploring low-cost sources for novel chiral solvents
resolves10.1021/la061688h
Adsorption and Aggregation Properties of Heterogemini Surfactants Containing a Quaternary Ammonium Salt and a Sugar Moiety
resolves10.1016/j.colsurfa.2008.05.036
Synthesis and aqueous solution properties of PAMAM dendron surfactants bearing a quaternary ammonium focal group and sugar terminal groups
resolves10.1007/s11743-014-1562-9
Sugar‐Based Ester Quaternary Ammonium Compounds and Their Surfactant Properties
resolves10.3906/kim-1711-35
Synthesis, characterization, and evaluation of toxicity of quaternary ammonium chlorides of glucose-based ester
resolves10.1016/j.jhazmat.2011.07.064
Mutagenicity of quaternary ammonium salts containing carbohydrate moieties
resolves10.3762/bjoc.12.138
Mutagenic activity of quaternary ammonium salt derivatives of carbohydrates
resolves10.1016/j.tetlet.2013.06.114
Synthesis of glucose-tagged triazolium ionic liquids and their application as solvent and ligand for copper(I) catalyzed amination
resolves10.3390/molecules180911512
Click Reactions as a Key Step for an Efficient and Selective Synthesis of D-Xylose-Based ILs
resolves10.1016/0008-6215(96)83597-X
A general method for synthesis of alkyl 2-N-substituted and 2-N,N-disubstituted d-altrosamines
resolves10.1002/hlca.19490320139
Über Steroide und Sexualhormone. 160. Mitteilung. 2α, 3α‐ und 2β, 3β‐Oxido‐chlolestane; Konfiguration der 2‐Oxy‐cholestane
resolves10.1055/s-1974-23284
Selective Sulphonylation with<i>N</i>-Tosylimidazole. A One-Step Preparation of Methyl 2,3-Anhydro-4,6-<i>O</i>-benzylidene-α-D-mannopyranoside
resolves10.1016/j.tet.2010.05.071
Synthesis and characterization of d-glucosamine-derived low molecular weight gelators
resolves10.1021/jo201179p
Stereoselective Synthesis of 2,3-Diamino-2,3-dideoxy-β-<scp>d</scp>-mannopyranosyl Uronates
resolves10.1071/CH9802509
Further stereoselective reductions of 3-O-hexofuranosyl S-methyl dithiocarbonates with tributyltin deuteride. A comment on mechanism
resolves10.1016/j.carres.2013.12.026
Preparation of new type of organocatalysts having a carbohydrate scaffold
resolves10.1021/ja973174y
A Rational Approach to Catalytic Enantioselective Enolate Alkylation Using a Structurally Rigidified and Defined Chiral Quaternary Ammonium Salt under Phase Transfer Conditions
resolves10.1021/ja991062w
Molecular Design of a <i>C</i><sub>2</sub>-Symmetric Chiral Phase-Transfer Catalyst for Practical Asymmetric Synthesis of <i>α</i>-Amino Acids
resolves10.1055/s-0032-1316804
Investigations Concerning the Syntheses of TADDOL-Derived Secondary Amines and Their Use To Access Novel Chiral Organocatalysts
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no DOI — not checkedCIT0018
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