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chemistry (12) 12
crystallography (8) 8
chemistry, organic (7) 7
organic papers (7) 7
catalysis (5) 5
derivatives (5) 5
single-crystal x-ray study (5) 5
baylis-hillman reaction (4) 4
chemistry, multidisciplinary (4) 4
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mean σ = 0.003 å (4) 4
t = 293 k (4) 4
1,3-dipolar cycloaddition (3) 3
cage compounds (3) 3
chemical synthesis (3) 3
cycloaddition (3) 3
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oxalic acid (2) 2
paper (2) 2
pyridine (2) 2
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1-oxa-1,3-butadienes (1) 1
[c-h center dot center dot center dot anion] interactions (1) 1
[chim]chemical sciences (1) 1
acetylcholinesterase (1) 1
acids (1) 1
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data-to-parameter ratio = 15.3 (1) 1
data-to-parameter ratio = 20.9 (1) 1
data-to-parameter ratio = 21.4 (1) 1
data-to-parameter ratio = 23.1 (1) 1
data-to-parameter ratio = 23.3 (1) 1
denitration (1) 1
diastereoselective syntheses, enantioselective syntheses (1) 1
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Chemistry – A European Journal, ISSN 0947-6539, 09/2018, Volume 24, Issue 52, pp. 13938 - 13946
Water‐soluble Pd12L6 coordination cage TC‐1 was synthesized by coordination‐driven self‐assembly of symmetrical tetrapyridyl donor L with 90° ditopic acceptor... 
self-assembly | palladium | cycloaddition | cage compounds | homogeneous catalysis | Nuclear magnetic resonance spectroscopy | Usage | Palladium | Catalysis | Magnetic resonance spectroscopy | Nitromethane | Cycloaddition | X-ray diffraction | Chemical reactions | Cages | Derivatives | NMR spectroscopy | Chemical synthesis | Conversion | Assembly
Journal Article
Chemical Communications, ISSN 1359-7345, 2018, Volume 54, Issue 38, pp. 4814 - 4817
The reaction of chiral cis-[(1S,2S)-dch]Pt(NO3)2 (M) [where (1S,2S)-dch = (1S,2S)-1,2-diaminocyclohexane] with a hexadentate ligand (L) in 3 : 1 stoichiometric... 
Self assembly | Chemical reactions | Cages | Catalysis | Molecular chains | Michael reaction
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 03/2014, Volume 2014, Issue 7, pp. 1505 - 1513
A highly efficient, multicomponent protocol for the construction of functionalized quinolinopyranpyrazole scaffolds with high stereoselectivity has been... 
Fused ring systems | Domino reactions | Multicomponent reactions | Nitrogen heterocycles | Diastereoselectivity | STRATEGY | BAYLIS-HILLMAN REACTION | CHEMISTRY, ORGANIC | DOMINO-REACTIONS | DIVERSITY-ORIENTED SYNTHESIS | CHEMISTRY | STEREOSELECTIVE-SYNTHESIS | TRANSFORMATIONS | Chromatography
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 11/2017, Volume 23, Issue 62, pp. 15704 - 15712
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 06/2015, Volume 56, Issue 25, pp. 3954 - 3960
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 05/2019, Volume 141, Issue 21, pp. 8638 - 8645
Journal Article
ISSN 1477-0520, 4/2019, Volume 17, Issue 16, pp. 3884 - 3893
A novel multicomponent quadruple domino reaction (MCQDR) for the assembly of structurally complex molecular architectures via the formation of three rings and... 
Journal Article
ISSN 1359-7345, 5/2018, Volume 54, Issue 38, pp. 4814 - 4817
The reaction of chiral cis -[(1 S ,2 S )- dch ]Pt(NO 3 ) 2 ( M ) [where (1 S ,2 S )- dch = (1 S ,2 S )-1,2-diaminocyclohexane] with a hexadentate ligand ( L )... 
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 08/2015, Volume 56, Issue 35, pp. 4980 - 4983
A convenient one-pot synthesis of 2-benzoxepines generated from (E)-2-nitro-3-arylprop-2-en-1-ols with paraformaldehyde via oxa-Pictet–Spengler cyclization is... 
Benzoxepinopyrrolidines/spiropyrrolidines | 1,3-Dipolar cycloaddition | Regioselectivity | Nitrobenzoxepines | TRANSFORMATION | ASPERGILLUS-FUMIGATUS | CHEMISTRY, ORGANIC | OXINDOLE | CARBONYL YLIDES | BAYLIS-HILLMAN ADDUCTS | TANDEM CONSTRUCTION | FACILE SYNTHESIS | HETEROCYCLES | CELL CYCLE INHIBITORS | DERIVATIVES | Oxalic acid | Schiff bases
Journal Article
Journal of Heterocyclic Chemistry, ISSN 0022-152X, 03/2015, Volume 52, Issue 2, p. 418
Journal Article
Journal of Heterocyclic Chemistry, ISSN 0022-152X, 03/2015, Volume 52, Issue 2, pp. 418 - 424
In this article, a simple method for the synthesis of bis(di(indolyl)aryl)methanes is described. The iodine‐catalyzed (5 mol %) reaction of indoles with... 
PRACTICAL SYNTHESIS | BIS(INDOLYL)METHANES | ACIDS | ACYLATION | CHEMISTRY, ORGANIC | CONDENSATION | CATALYST | EFFICIENT | INDOLES | ZINC-OXIDE ZNO
Journal Article
Chemistry - A European Journal, ISSN 0947-6539, 09/2018, Volume 24, Issue 52, pp. 13938 - 13946
Water-soluble Pd12L6 coordination cage TC-1 was synthesized by coordination-driven self-assembly of symmetrical tetrapyridyl donor L with 90 degrees ditopic... 
self-assembly | palladium | cycloaddition | cage compounds | homogeneous catalysis | COORDINATION CHEMISTRY | CATALYSIS | CHEMISTRY, MULTIDISCIPLINARY | GUEST INCLUSION | DIELS-ALDER REACTION | X-RAY | MEDIA | LIGAND | MOLECULAR CAPSULE | ARCHITECTURES | WATER
Journal Article
ORGANIC & BIOMOLECULAR CHEMISTRY, ISSN 1477-0520, 04/2019, Volume 17, Issue 16, pp. 3884 - 3893
A novel multicomponent quadruple domino reaction (MCQDR) for the assembly of structurally complex molecular architectures via the formation of three rings and... 
MILD | STRATEGY | COMPLEXITY | CHEMISTRY | CHEMISTRY, ORGANIC | CASCADE | FLAVONOIDS | DERIVATIVES | DRAGONS BLOOD | FRAMEWORKS
Journal Article
CHEMICAL COMMUNICATIONS, ISSN 1359-7345, 05/2018, Volume 54, Issue 38, pp. 4814 - 4817
The reaction of chiral cis-[(1S,2S)-dch] Pt(NO3)(2) (M) [where (1S,2S)-dch = (1S,2S)-1,2-diaminocyclohexane] with a hexadentate ligand (L) in 3 : 1... 
DIELS-ALDER | MOLECULAR RECOGNITION | STABILIZATION | ENCAPSULATION | COMPLEXES | SUPRAMOLECULAR CLUSTER | CHEMISTRY, MULTIDISCIPLINARY | HOST-GUEST | SYNTHETIC RECEPTOR | INDOLES | WATER
Journal Article
RSC Advances, ISSN 2046-2069, 2015, Volume 5, Issue 113, pp. 93447 - 93451
In this paper, an elegant synthesis of 1,2,3-triazole derivatives via domino [3 + 2] azide cycloaddition and denitration reaction sequence under catalyst free... 
ACETYLCHOLINESTERASE | ONE-POT SYNTHESIS | ANALOGS | 1,3-DIPOLAR CYCLOADDITION | NITROOLEFINS | CLICK-CHEMISTRY | ORGANIC AZIDES | ALKYNES | REGIOSELECTIVITY | CHEMISTRY, MULTIDISCIPLINARY | IN-SITU
Journal Article
Acta Crystallographica Section E: Structure Reports Online, ISSN 1600-5368, 03/2014, Volume 70, Issue 3, pp. o299 - o300
In the title compound, C29H29BrN2O3, the indole ring system is essentially planar (r.m.s. deviation = 0.079 angstrom) and makes a dihedral angle of 85.23... 
R factor = 0.035 | Mean σ(C-C) = 0.003 Å | T = 293 K | Data-to-parameter ratio = 15.3 | wR factor = 0.097 | Single-crystal X-ray study | CRYSTALLOGRAPHY
Journal Article
Acta Crystallographica Section E: Structure Reports Online, ISSN 1600-5368, 03/2014, Volume 70, Issue 3, pp. o272 - O272
In the title compound, C30H30Cl2N2O3, the indole ring system is roughly planar, with a maximum deviation of 0.1039 (18) angstrom for the carbonyl C atom, and... 
wR factor = 0.167 | Mean σ(C-C) = 0.003 Å | T = 293 K | Data-to-parameter ratio = 23.1 | R factor = 0.051 | Single-crystal X-ray study | CRYSTALLOGRAPHY
Journal Article
Synthesis, ISSN 0039-7881, 02/2011, Volume 2011, Issue 4, pp. 611 - 618
Abstract For the first time Baylis-Hillman adducts derived from nitroolefins have been conveniently transformed into a novel class of building blocks,... 
paper | hydrobromic acid | nitroalkenes | Baylis-Hillman reaction | ammonium acetate | iron(III) chloride | CONJUGATED NITROALKENES | AMINO-ACIDS | CHEMISTRY | PROTOCOL | CHEMISTRY, ORGANIC | CYCLIZATION | FRAMEWORKS
Journal Article
Journal of the American Chemical Society, 05/2019, Volume 141, Issue 21, p. 8638
Donor-acceptor Stenhouse adducts (DASA) are new-generation photochromic compounds discovered recently. DASA exist normally in open form (blue/violet) and... 
Journal Article
Acta Crystallographica Section E: Structure Reports Online, ISSN 1600-5368, 03/2014, Volume 70, Issue 3, pp. o335 - O335
In the title compound, C27H24Cl2N2O3, the indole ring system is essentially planar, with a maximum deviation of 0.082 (2) angstrom for the carbonyl C atom. It... 
Mean σ(C-C) = 0.003 Å | R factor = 0.044 | wR factor = 0.124 | Data-to-parameter ratio = 20.9 | T = 293 K | Single-crystal X-ray study | CRYSTALLOGRAPHY
Journal Article
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