Keywords: Acac; acetylacetonate; Ar; aryl; Bn; benzyl; Br; bromo; Bu; butyl; Cl; chloro; Cu; copper; DCM; dichloromethane; DMF; dimethylformamide; Et; ethyl; H; hour; Hpp; 1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-a]pyrimidinate; iPr; iso-propyl; K; potassium; Me; meth
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Keywords: CS; chitosan; DFT; density functional theory; FTBH; Formaldehyde tert-butyl hydrazone; HOBt; 1-Hydroxybenzotriazole hydrate; TBME; tert-Butyl methyl ether; TMSCN; Trimethylsilyl cyanide; Acetophenone (PubChem CID: 7410); Ethyl benzoylformate (PubChem CID:
Keywords: Ac; acetyl; acac; acetylacetonate; AHPCS; allylhydridopolycarbosilane; Bn; benzyl; Boc; tert-butoxycarbonyl; BPR; back pressure regulator; bpy; 2,2â²-bipyridine; Bu; butyl; CFL; compact fluorescent lamp; DCB; 1,4-dicyanobenzene; de; diastereomeric excess
Keywords: Diversity-oriented synthesis; Imidazoheterocyclic; Groebke-Blackburn-Bienayme reaction; Fused imidazole; Lewis acid; Ugi type; Ac; acetyl; Aq; aqueous; Ar; aryl; Bn; benzyl; Boc; tert-butoxycarbonyl; BDMS; bromodimethylsulfonium bromide; CDK; cyclin-d
Synthesis of MOFs for heterogeneous catalysis via linker design
Keywords: MOFs; metal-organic frameworks; PCNs; porous coordination networks; PCPs; porous coordination polymers; PSM; post-synthetic modifications; SBUs; secondary building units; TCPP; tetrakis(4-carboxyphenyl)porphyrin); MMPF; metal-metalloporphyrin framework;
Octahedra-based molecular sieve aluminoborate (PKU-1) as solid acid for heterogeneously catalyzed Strecker reaction
Keywords: JOZSADTXGKNKEG-WJHHQPKCSA-NAluminoborate; Solid acid; α-Aminonitriles; TMSCN; Mechanism
Synthesis, characterization and catalytic property of chiral oxo-vanadium (+)-pseudoephedrine complex supported on magnetic nanoparticles Fe3O4 in the cyanosilylation of carbonyl compounds
Keywords: Carbonyl compounds; TMSCN; Oxovanadium–(+)-pseudoephedrine complex; Magnetically catalyst
Direct oxidative cyanation of tertiary amines promoted by in situ generated hypervalent iodine(III)-CN intermediate
Keywords: α-Aminonitriles; Cyanation; N,N-Dialkylanilines; Hypervalent iodine; TMSCN;
Thiamine hydrochloride (VB1)-catalyzed one-pot synthesis of (E)-N-benzylidene-2-phenyl-1H-benzo[d]imidazo[1,2-a]imidazol-3-amine derivatives
Keywords: Multi-component reaction; Thiamine hydrochloride (VB1); Green chemistry; 2-Aminobenzimidazole; TMSCN;
Sulfated tungstate: a green catalyst for Strecker reaction
Keywords: Sulfated tungstate; Strecker reaction; α-Aminonitriles; TMSCN;
Highly efficient and convenient Strecker reaction of carbonyl compounds and amines with TMSCN catalyzed by MCM-41 anchored sulfonic acid as a recoverable catalyst
Keywords: MCM-41-SO3H nanocatalyst; Solid acid; Strecker reaction; α-Amino nitriles; Carbonyl compounds; TMSCN;
Oxalic acid as a simple and efficient organocatalyst for three-component synthesis of α-amino nitriles
Keywords: Oxalic acid; TMSCN; Brønsted acid; α-Amino nitriles
Highly active bifunctional salenTi(IV) catalysts for asymmetric cyanosilylation of aldehydes and TMSCN
Keywords: Cyanohydrin; Bifunctional catalyst; Salen; TMSCN; Diphenylphosphine oxide
Nano-ordered B-MCM-41: An efficient and recoverable solid acid catalyst for three-component Strecker reaction of carbonyl compounds, amines and TMSCN
Keywords: Nano-ordered borosilicate (B-MCM-41); Multi-component reactions; Strecker reaction; αα-amino nitriles; Carbonyl compounds; TMSCN
Design and synthesis of 3-pyridylacetamide derivatives as dipeptidyl peptidase IV (DPP-4) inhibitors targeting a bidentate interaction with Arg125
Keywords: DPP-4; Dipeptidyl peptidase IV; GLP-1; Glucagon-like peptide 1; SAR; Structure-activity relationship; AcOH; Acetic acid; DIBAL-H; Diisobutylaluminum hydride; Boc; tert-Butoxy carbonyl; TMSCN; Trimethylsilyl cyanide; TBAF; Tetrabutylammonium fluoride; mC
Synthetic application of in situ generation of N-acyliminium ions from α-amido p-tolylsulfones for the synthesis of α-amino nitriles
Keywords: α-Amido p-tolylsulfones; TMSCN; α-Amino nitriles; N-Acyliminum ions; Bismuth bromide;
Convenient and rapid synthesis of α-aminonitriles starting directly from nitro compounds in water
Keywords: α-Aminonitriles; Nitro compound; In/HCl; TMSCN; Aqueous medium;
One-pot three components synthesis of O-acetylcyanohydrins with TMSCN, acetic anhydride and carbonyl compounds under solvent-free condition
Keywords: Aldehydes; Ketones; TMSCN; Acetic anhydride; B(C6F5)3; O-Acetylcyanohydrin;
Highly efficient chemo- and regioselective silylation of –OH groups and cyanosilylation of aldehydes promoted by TiCl2(OTf)–SiO2 as a new recyclable catalyst
Keywords: α-Hydroxyphosphonate; HMDS; Aldehyde; TMSCN; Cyanosilylation; Silica gel
Ionic liquid-promoted one-pot oxidative Michael addition of TMSCN to Baylis-Hillman adducts
Keywords: Baylis-Hillman adducts; Ionic liquids; Hypervalent iodine; Oxidation; Michael addition; TMSCN;
Computational study on 1,1,3,3-tetramethylguanidine-catalyzed cyanosilylation mechanism of hypnone
Keywords: Cyanosilylation; Hypnone; TMG; TMSCN; B3LYP;
Cyanosilylation at pregnane side-chains
Keywords: Cyanohydrins; Stereoselectivity; Steroids; Pregnanes; TMSCN; X-Ray;
Acyclic α-nitro ketones: a versatile class of α-functionalized ketones in organic synthesis
Keywords: α-Nitro ketones; Acyclic; Organic synthesis; AIBN; azobisisobutyronitrile; ALA-5; δ-aminolevulinic acid; CIMP; 2-chloro-5-iodomethylpyridine; DBU; 1,8-diazobicyclo[5.4.0]undec-7-ene; DCC; dicyclohexylcarbodiimide; DHRGC; dynamic high-resolution gas chro