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Tetrahedron, ISSN 0040-4020, 06/2015, Volume 71, Issue 24, pp. 4219 - 4226
A simple, cheap, efficient, and metal-free method for one-step synthesis of a library of 1,3-diheteroatom five-membered heterocycles with exocyclic CN and CC... 
Heterocycles | Metal-free | Iodocyclization | Propargylamines
Journal Article
Chemical Society Reviews, ISSN 0306-0012, 08/2014, Volume 43, Issue 16, pp. 5750 - 5765
Metal-organic frameworks (MOFs) are finding increasing application as solid catalysts for liquid phase reactions leading to the synthesis of fine chemicals. In... 
EFFICIENT HETEROGENEOUS CATALYST | DESIGN | ROBUST | PHARMACOLOGY | ARYLATION | QUINOLINES | PROPARGYLAMINES | COPPER | MOFS | PALLADIUM NANOPARTICLES | CHEMISTRY, MULTIDISCIPLINARY
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 10/2007, Volume 48, Issue 40, pp. 7184 - 7190
An inexpensive and readily available catalyst, Zn(OAc) ·2H O is successfully evaluated for effective one-pot synthesis of propargylamines with moderate to... 
Catalysis | Zinc acetate | Three-component coupling | Propargylamines
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 04/2010, Volume 51, Issue 14, pp. 1891 - 1895
Magnetically separable Fe O nanoparticles endow with an efficient and economic route for the synthesis of propargylamines by the three-component coupling of... 
Amines | nanoparticles | Terminal alkynes | Aldehydes | Propargylamines | Magnetically separable Fe
Journal Article
RSC Advances, ISSN 2046-2069, 2019, Volume 9, Issue 10, pp. 5475 - 5479
Atomically precise Au-13 nanoclusters stabilized by stibines catalyze the aldehyde-alkyne-amine coupling reaction more efficiently than those stabilized by... 
PROPARGYLAMINES | CHEMISTRY, MULTIDISCIPLINARY | GOLD CLUSTERS
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 05/2018, Volume 59, Issue 21, pp. 1986 - 1991
[Display omitted] •Utilization of abundantly available, renewable and biodegradable polymeric support.•Waste-free approach for the synthesis of propargylamine... 
Heterogeneous catalyst | Decarboxylative A3-coupling | Chitosan | Recyclability | Propargylamines | coupling | Decarboxylative A
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 03/2019, Volume 2019, Issue 10, pp. 1981 - 1985
A copper(I) bromide‐catalyzed reaction of A3‐coupling‐derived propargylamines with ethyl buta‐2,3‐dienoate for the fast assembly of a 1,6‐dihydropyridine core... 
Allenes | Dihydropyridines | Cyclization | Copper | Propargylamines | GOLD | CHEMISTRY, ORGANIC | ALKYNES | AMINE | POLYSUBSTITUTED PYRROLES | N-PROPARGYLAMINES | CYCLOISOMERIZATION | SELECTIVE SYNTHESIS | BETA-ENAMINONES | FACILE | ACCESS
Journal Article
Chemistry Letters, ISSN 0366-7022, 12/2016, Volume 45, Issue 12, pp. 1457 - 1459
In this study, we report a thiolate-protected Au nanocluster, Au25(phenylethanethiol)18 [Au25(PET)18], which serves as an efficient catalyst by a... 
Propargylamine | Gold nanocluster catalyst | Alkyne
Journal Article
Chemical Society Reviews, ISSN 0306-0012, 7/2014, Volume 43, Issue 16, pp. 575 - 5765
Metal-organic frameworks (MOFs) are finding increasing application as solid catalysts for liquid phase reactions leading to the synthesis of fine chemicals. In... 
Synthesis (chemistry) | Synthesis | Catalysts | Imidazole | Liquid phases | Metalorganic compounds | Catalysis | Metal-organic frameworks | Organic compounds
Journal Article
Catalysis Communications, ISSN 1566-7367, 08/2012, Volume 25, pp. 50 - 53
Recyclable ZnO nano particles (ZnO NPs) provide an efficient and economic route for synthesis of multi component A coupling reaction of propargylamines under... 
Excellent yields | Zinc oxide | Propargylamines | Catalyst
Journal Article
Journal of Molecular Catalysis A: Chemical, ISSN 1381-1169, 2014, Volume 381, pp. 126 - 131
Nano-size ZnS was prepared by a simple, economic and elegant chemical bath deposition technique and characterized by using SEM, TEM, XRD, and EDAX techniques.... 
Heterogeneous and recyclable catalyst | coupling reaction | Nano-size ZnS | Propargylamines
Journal Article
Chemistry Letters, ISSN 0366-7022, 11/2017, Volume 46, Issue 11, pp. 1620 - 1623
A novel (PNO)Rh/CuBr (PNO: phosphine-quinolinolate) tandem catalyst system was developed for facile synthesis of α-monosubstituted propargylamines from... 
Propargylamines | Terminal alkynes | Rhodium catalysts | ADDITION-REACTION | IMINES | MARKOVNIKOV HYDROAMINATION-ALKYNYLATION | ENAMINES | GAMMA,DELTA-ALKYNYL-BETA-AMINO ACID-DERIVATIVES | CHEMISTRY, MULTIDISCIPLINARY | N-PROPARGYLAMINES | ARYLACETYLENES | METAL CATALYSIS | ACCESS
Journal Article
Chemical Science, ISSN 2041-6520, 2016, Volume 7, Issue 6, pp. 3914 - 3918
Methods to incorporate atmospheric CO2 into organic molecules are on demand. Here we present two Pdcatalyzed multicomponent reactions that provide... 
TRANSFORMATION | MULTICOMPONENT REACTIONS | 2-OXAZOLIDINONES | ACETYLENIC AMINES | COMPLEXES | PROPARGYLAMINES | CARBOXYLATIVE CYCLIZATION | IONIC LIQUIDS | CARBON-DIOXIDE | DERIVATIVES | CHEMISTRY, MULTIDISCIPLINARY
Journal Article
Chemical Science, ISSN 2041-6520, 2016, Volume 7, Issue 6, pp. 3914 - 3918
Methods to incorporate atmospheric CO2 into organic molecules are on demand. Here we present two Pd-catalyzed multicomponent reactions that provide... 
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 09/2016, Volume 81, Issue 18, pp. 8135 - 8141
A Au­(III)-catalyzed regiospecific hydration of N-(diphenylphosphinoyl)­propargyl amines has been developed to produce various β-amino ketones. These reactions... 
ACIDS | IMINES | COMPLEXES | PROPARGYLAMINES | CHEMISTRY, ORGANIC | TERMINAL ALKYNES | EFFICIENT
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 09/2018, Volume 2018, Issue 35, pp. 4845 - 4849
A one‐pot transition metal‐free synthesis of propargylamines in good to excellent yield from ketone‐derived imines and aryl‐ and hetarylacetylenes in the... 
Ethynylation | Acetylenes | Ketimines | Propargylamines | Superbases | SINGLE | PROPARGYLAMINE | MULTIFUNCTIONAL DRUGS | NANOPARTICLE | CHEMISTRY, ORGANIC | ALDEHYDES | ALKYNE | COUPLING REACTION | DERIVATIVES | ALZHEIMERS | Schiff bases
Journal Article
Organic Letters, ISSN 1523-7060, 10/2015, Volume 17, Issue 19, pp. 4842 - 4845
The highly stereoselective addition of lithiated chloroacetylene, derived in situ from cis-1,2-dichloroethene and methyl lithium, to Ellman chiral... 
CHIRAL PROPARGYLAMINES | ALDIMINES | PROMOTED DIASTEREOSELECTIVE SYNTHESIS | ASYMMETRIC-SYNTHESIS | AMINES | OPTICALLY-ACTIVE PROPARGYLAMINES | CHEMISTRY, ORGANIC | ZINC/BINOL-CATALYZED ALKYNYLATION | CYCLOISOMERIZATION | ALDEHYDES | ENANTIOSELECTIVE 3-COMPONENT SYNTHESIS
Journal Article
Organic Letters, ISSN 1523-7060, 04/2009, Volume 11, Issue 8, pp. 1701 - 1704
FeCl2 catalyzes the oxidative C−C cross-coupling of tertiary amines with terminal alkynes into propargylamines using (t-BuO)2 as oxidant. The reaction can be... 
PEROXIDASE | DIRECT ARYLATION | ALKYLATION | NITROGEN ATOM | COMPOUND | PROPARGYLAMINES | CHEMISTRY, ORGANIC | METAL | ARYL | ADJACENT | MOLECULAR-OXYGEN
Journal Article
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