Tetrahedron Letters, ISSN 0040-4039, 06/2018, Volume 59, Issue 24, pp. 2347 - 2351
An efficient and simple approach for the synthesis of functionalized 4 -chromenes has been developed via acid catalyzed Michael addition of phenols to...
Michael addition | Benzylidene oxobutanoates | 4H-Chromenes | Linear pyranocoumarins | Angular pyranocoumarins | ONE-POT SYNTHESIS | FUNCTIONALIZED 4H-CHROMENES | 3-COMPONENT REACTION | BENZYLATION | CHEMISTRY, ORGANIC | ADDITION/ANNULATION | COUMARINS | TANDEM REACTION | SELECTIVE SYNTHESIS | DERIVATIVES | EFFICIENT | Phenols | Nuclear magnetic resonance spectroscopy | Analysis
Michael addition | Benzylidene oxobutanoates | 4H-Chromenes | Linear pyranocoumarins | Angular pyranocoumarins | ONE-POT SYNTHESIS | FUNCTIONALIZED 4H-CHROMENES | 3-COMPONENT REACTION | BENZYLATION | CHEMISTRY, ORGANIC | ADDITION/ANNULATION | COUMARINS | TANDEM REACTION | SELECTIVE SYNTHESIS | DERIVATIVES | EFFICIENT | Phenols | Nuclear magnetic resonance spectroscopy | Analysis
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 07/2014, Volume 53, Issue 30, pp. 7923 - 7927
We describe herein a catalytic, enantioselective process for the synthesis of 4H‐chromenes which are important structural elements of many natural products and...
benzhydrylic alcohols | asymmetric synthesis | chromenes | xanthenones | chiral phosphoric acids | ASYMMETRIC CATALYSIS | ONE-POT SYNTHESIS | ANNULATION | FUNCTIONALIZED 4H-CHROMENES | BOND-FORMING REACTIONS | SALICYL N-TOSYLIMINES | CHEMISTRY, MULTIDISCIPLINARY | FACILE CONSTRUCTION | SELECTIVE SYNTHESIS | EFFICIENT
benzhydrylic alcohols | asymmetric synthesis | chromenes | xanthenones | chiral phosphoric acids | ASYMMETRIC CATALYSIS | ONE-POT SYNTHESIS | ANNULATION | FUNCTIONALIZED 4H-CHROMENES | BOND-FORMING REACTIONS | SALICYL N-TOSYLIMINES | CHEMISTRY, MULTIDISCIPLINARY | FACILE CONSTRUCTION | SELECTIVE SYNTHESIS | EFFICIENT
Journal Article
Synlett, ISSN 0936-5214, 07/2014, Volume 25, Issue 11, pp. 1571 - 1576
Abstract A simple and efficient method has been developed for the synthesis of 4 H -chromenes from o -hydroxybenzylic alcohols and dicarbonyl compounds...
letter | supported reagents | ANNULATION | FUNCTIONALIZED 4H-CHROMENES | CHEMISTRY, ORGANIC | cyclizations | benzylations | ALCOHOLS | KETONES | chromenes | PHENOLS | FACILE CONSTRUCTION | one-pot syntheses | EFFICIENT | 2H-CHROMENES
letter | supported reagents | ANNULATION | FUNCTIONALIZED 4H-CHROMENES | CHEMISTRY, ORGANIC | cyclizations | benzylations | ALCOHOLS | KETONES | chromenes | PHENOLS | FACILE CONSTRUCTION | one-pot syntheses | EFFICIENT | 2H-CHROMENES
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 03/2015, Volume 357, Issue 5, pp. 967 - 973
The first organocatalytic asymmetric synthesis of 4H‐chromenes bearing a trifluoromethylated tetrasubstituted carbon center is presented. Chiral secondary...
organocatalysis | iminium–allenamine activation | trifluoromethylated tetrasubstituted carbon center | cascade reaction | 4H‐chromenes | 4H-chromenes | iminium-allenamine activation | ASYMMETRIC-SYNTHESIS | DOMINO REACTIONS | PRIVILEGED STRUCTURES | ONE-POT SYNTHESIS | COMBINATORIAL LIBRARIES | QUATERNARY STEREOCENTERS | CHEMISTRY, ORGANIC | MEDICINAL CHEMISTRY | BETA,BETA-DISUBSTITUTED ENONES | FACILE CONSTRUCTION | DENSELY FUNCTIONALIZED 4H-CHROMENES | CHEMISTRY, APPLIED | Uighurs | Synthesis | Catalysis | Oxalic acid | Enantiomers | Organic compounds | Amines | Asymmetry | Cascades | Activation | Maintenance | Carbon | Bearing
organocatalysis | iminium–allenamine activation | trifluoromethylated tetrasubstituted carbon center | cascade reaction | 4H‐chromenes | 4H-chromenes | iminium-allenamine activation | ASYMMETRIC-SYNTHESIS | DOMINO REACTIONS | PRIVILEGED STRUCTURES | ONE-POT SYNTHESIS | COMBINATORIAL LIBRARIES | QUATERNARY STEREOCENTERS | CHEMISTRY, ORGANIC | MEDICINAL CHEMISTRY | BETA,BETA-DISUBSTITUTED ENONES | FACILE CONSTRUCTION | DENSELY FUNCTIONALIZED 4H-CHROMENES | CHEMISTRY, APPLIED | Uighurs | Synthesis | Catalysis | Oxalic acid | Enantiomers | Organic compounds | Amines | Asymmetry | Cascades | Activation | Maintenance | Carbon | Bearing
Journal Article
Tetrahedron, ISSN 0040-4020, 11/2009, Volume 65, Issue 45, pp. 9152 - 9156
Et N-catalyzed reactions of salicyl N-tosylimines or salicylaldehydes with methyl 2-perfluoroalkynoates proceed smoothly at room temperature in dichloromethane...
Salicyl N-tosylimine | Regioselectivity | 2-(Perfluoroalkyl)-4H-chromene | Methyl 2-perfluoroalkynoate | Salicylaldehyde | HIGHLY FUNCTIONALIZED CHROMENES | 4-ARYL-4H-CHROMENES | BAYLIS-HILLMAN MECHANISM | CHEMISTRY, ORGANIC | DABCO-CATALYZED REACTION | 4H-CHROMENES | ACYCLIC PRECURSORS | FACILE SYNTHESIS | THROUGHPUT SCREENING ASSAY | ESTERS | DERIVATIVES | Analysis | Dimethyl sulfoxide
Salicyl N-tosylimine | Regioselectivity | 2-(Perfluoroalkyl)-4H-chromene | Methyl 2-perfluoroalkynoate | Salicylaldehyde | HIGHLY FUNCTIONALIZED CHROMENES | 4-ARYL-4H-CHROMENES | BAYLIS-HILLMAN MECHANISM | CHEMISTRY, ORGANIC | DABCO-CATALYZED REACTION | 4H-CHROMENES | ACYCLIC PRECURSORS | FACILE SYNTHESIS | THROUGHPUT SCREENING ASSAY | ESTERS | DERIVATIVES | Analysis | Dimethyl sulfoxide
Journal Article
中国化学快报:英文版, ISSN 1001-8417, 2012, Volume 23, Issue 10, pp. 1129 - 1132
A Cu(I)-catalyzed one-pot tandem reaction of 2-bromobenzyl bromides with 1,3-dicarbonyl compounds leading to 4H- chromene derivatives has been developed. This...
二羰基化合物 | 苄基 | Cu(Ⅰ) | 衍生物 | 苯并吡喃 | 溴化物 | 串联反应 | 铜催化 | Copper catalysis | 4H-Chromenes | One-pot tandem reaction | HIGHLY FUNCTIONALIZED CHROMENES | ORGANIC-SYNTHESIS | ARYLATION | SALICYL N-TOSYLIMINES | CHEMISTRY, MULTIDISCIPLINARY | KETONES | CASCADE PROCESS | DERIVATIVES | 2H-CHROMENES | CYCLIZATION
二羰基化合物 | 苄基 | Cu(Ⅰ) | 衍生物 | 苯并吡喃 | 溴化物 | 串联反应 | 铜催化 | Copper catalysis | 4H-Chromenes | One-pot tandem reaction | HIGHLY FUNCTIONALIZED CHROMENES | ORGANIC-SYNTHESIS | ARYLATION | SALICYL N-TOSYLIMINES | CHEMISTRY, MULTIDISCIPLINARY | KETONES | CASCADE PROCESS | DERIVATIVES | 2H-CHROMENES | CYCLIZATION
Journal Article
中国化学:英文版, ISSN 1001-604X, 2012, Volume 30, Issue 8, pp. 1709 - 1714
An efficient and environmentally benign procedure for the reactions of three components condensation of sali- cylaldehyde and two different CH acids to give...
催化 | 合成 | 实验 | 一锅法 | 吡喃 | 离子液体 | 功能化 | 氨基 | basic‐functionalized ionic liquid | one‐pot synthesis | 2‐amino‐4H‐chromene | density functional theory | 2-amino-4H-chromene | basic-functionalized ionic liquid | one-pot synthesis | 3-COMPONENT SYNTHESIS | GREEN SYNTHESIS | MEDIA | ALDEHYDES | DERIVATIVES | EFFICIENT | CHEMISTRY, MULTIDISCIPLINARY | CO2 CAPTURE | Hydrogen | Hydrogen bonding | Green chemistry
催化 | 合成 | 实验 | 一锅法 | 吡喃 | 离子液体 | 功能化 | 氨基 | basic‐functionalized ionic liquid | one‐pot synthesis | 2‐amino‐4H‐chromene | density functional theory | 2-amino-4H-chromene | basic-functionalized ionic liquid | one-pot synthesis | 3-COMPONENT SYNTHESIS | GREEN SYNTHESIS | MEDIA | ALDEHYDES | DERIVATIVES | EFFICIENT | CHEMISTRY, MULTIDISCIPLINARY | CO2 CAPTURE | Hydrogen | Hydrogen bonding | Green chemistry
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 02/2019, Volume 60, Issue 7, pp. 538 - 540
A strategically new approach to 9-substituted 2,3,4,9-tetrahydro-1 -xanthen-1-ones is described. The protocol includes TMG promoted, conjugate addition of...
Michael addition | HWE olefination | Coumarins | 1,1,3,3-Tetramethylguanidine | Cyclohexane-1,3-diones | Tetrahydroxanthenones | PHLOROGLUCINOL | ONE-POT | FUNCTIONALIZED 4H-CHROMENES | CHEMISTRY, ORGANIC
Michael addition | HWE olefination | Coumarins | 1,1,3,3-Tetramethylguanidine | Cyclohexane-1,3-diones | Tetrahydroxanthenones | PHLOROGLUCINOL | ONE-POT | FUNCTIONALIZED 4H-CHROMENES | CHEMISTRY, ORGANIC
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 11/2015, Volume 80, Issue 21, pp. 11048 - 11056
Cesium carbonate-mediated reaction of 2-hydroxybenzaldehydes and 2-bromoallyl sulfones afforded 2H- and 4H-chromenol derivatives endowed with a 3-arylsulfonyl...
L-PROLINE | SALICYLIC ALDEHYDES | FUNCTIONALIZED 4H-CHROMENES | CATALYZED SYNTHESIS | THROUGHPUT SCREENING ASSAY | ALPHA,BETA-UNSATURATED ALDEHYDES | CHEMISTRY, ORGANIC | SELECTIVE SYNTHESIS | SUBSTITUTED 4H-CHROMENES | EFFICIENT | 2H-CHROMENES
L-PROLINE | SALICYLIC ALDEHYDES | FUNCTIONALIZED 4H-CHROMENES | CATALYZED SYNTHESIS | THROUGHPUT SCREENING ASSAY | ALPHA,BETA-UNSATURATED ALDEHYDES | CHEMISTRY, ORGANIC | SELECTIVE SYNTHESIS | SUBSTITUTED 4H-CHROMENES | EFFICIENT | 2H-CHROMENES
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 03/2016, Volume 81, Issue 5, pp. 2062 - 2069
An efficient, environmentally friendly and one-pot route to new 9-aryl/9-arylethynyl-2,3,4,9-tetrahydro-1H-xanthen-1-one derivatives from inexpensive starting...
CATALYSIS | DYES | EFFICIENT APPROACH | FUNCTIONALIZED 4H-CHROMENES | XANTHENE DERIVATIVES | AQUEOUS-MEDIA | CHEMISTRY, ORGANIC | CASCADE | 2,3,4,9-TETRAHYDRO-1H-XANTHEN-1-ONES | XANTHONES | CYCLIZATION | Usage | Amines | Iron compounds | Chemical properties | Ring formation (Chemistry)
CATALYSIS | DYES | EFFICIENT APPROACH | FUNCTIONALIZED 4H-CHROMENES | XANTHENE DERIVATIVES | AQUEOUS-MEDIA | CHEMISTRY, ORGANIC | CASCADE | 2,3,4,9-TETRAHYDRO-1H-XANTHEN-1-ONES | XANTHONES | CYCLIZATION | Usage | Amines | Iron compounds | Chemical properties | Ring formation (Chemistry)
Journal Article
ACS Combinatorial Science, ISSN 2156-8952, 11/2013, Volume 15, Issue 11, pp. 557 - 563
An efficient one-pot synthesis of functionalized 2-amino-4H-pyrans by a meglumine-catalyzed three-component reaction has been developed. A broad range of...
functionalized 2-amino-4 H -pyrans | meglumine | three-component reaction | functionalized 2-amino-4H-pyrans | one-pot synthesis | CHEMISTRY, MEDICINAL | ACID | AQUEOUS-MEDIA | MAGNETICALLY SEPARABLE CATALYST | IONIC LIQUID | CHEMISTRY, MULTIDISCIPLINARY | MULTICOMPONENT REACTIONS | VERSATILE CATALYST | GREEN SYNTHESIS | RECYCLABLE CATALYST | SUBSTITUTED 4H-CHROMENES | CHEMISTRY, APPLIED | DERIVATIVES | Pyrans - chemical synthesis | Molecular Structure | Combinatorial Chemistry Techniques | Catalysis | Meglumine - chemistry | Pyrans - chemistry | Activated | Construction | Synthesis | Aromatic compounds | Condensing | Libraries | Derivatives | Combinatorial analysis
functionalized 2-amino-4 H -pyrans | meglumine | three-component reaction | functionalized 2-amino-4H-pyrans | one-pot synthesis | CHEMISTRY, MEDICINAL | ACID | AQUEOUS-MEDIA | MAGNETICALLY SEPARABLE CATALYST | IONIC LIQUID | CHEMISTRY, MULTIDISCIPLINARY | MULTICOMPONENT REACTIONS | VERSATILE CATALYST | GREEN SYNTHESIS | RECYCLABLE CATALYST | SUBSTITUTED 4H-CHROMENES | CHEMISTRY, APPLIED | DERIVATIVES | Pyrans - chemical synthesis | Molecular Structure | Combinatorial Chemistry Techniques | Catalysis | Meglumine - chemistry | Pyrans - chemistry | Activated | Construction | Synthesis | Aromatic compounds | Condensing | Libraries | Derivatives | Combinatorial analysis
Journal Article
New Journal of Chemistry, ISSN 1144-0546, 2017, Volume 41, Issue 17, pp. 9388 - 9396
A series of newly synthesized 4-(1H-indol-3-yl)-2-methyl-N-phenyl-4H-chromene-3-carboxamide derivatives were achieved by one-pot reaction between...
ANTICANCER ACTIVITY | 3 COMPONENT REACTIONS | PHENOLS | FACILE CONSTRUCTION | DENSELY FUNCTIONALIZED 4H-CHROMENES | TANDEM REACTION | CATALYST | DERIVATIVES | EFFICIENT | CHEMISTRY, MULTIDISCIPLINARY | SOLVENT-FREE SYNTHESIS
ANTICANCER ACTIVITY | 3 COMPONENT REACTIONS | PHENOLS | FACILE CONSTRUCTION | DENSELY FUNCTIONALIZED 4H-CHROMENES | TANDEM REACTION | CATALYST | DERIVATIVES | EFFICIENT | CHEMISTRY, MULTIDISCIPLINARY | SOLVENT-FREE SYNTHESIS
Journal Article
RSC Adv, ISSN 2046-2069, 2014, Volume 4, Issue 26, pp. 13708 - 13718
A new concept of catalysts which are prepared from renewable materials is demonstrated. It is known that amino acids (e.g., proline and hydroxyproline) are...
Journal Article
TETRAHEDRON LETTERS, ISSN 0040-4039, 01/2016, Volume 57, Issue 1, pp. 141 - 145
A facile and efficient method for the synthesis of 1-oxo-hexahydroxanthenes catalyzed by FeCl3 center dot 6H(2)O is described. The iron-catalyzed condensation...
ACID | FUNCTIONALIZED 4H-CHROMENES | ORGANOCATALYST | CHEMISTRY, ORGANIC | AROMATIC-ALDEHYDES | Catalytic reactions | FeCl3 center dot 6HO | XANTHONES | Organic synthesis | 1-Oxo-hexahydroxanthenes | Green chemistry | DERIVATIVES | EFFICIENT | WATER
ACID | FUNCTIONALIZED 4H-CHROMENES | ORGANOCATALYST | CHEMISTRY, ORGANIC | AROMATIC-ALDEHYDES | Catalytic reactions | FeCl3 center dot 6HO | XANTHONES | Organic synthesis | 1-Oxo-hexahydroxanthenes | Green chemistry | DERIVATIVES | EFFICIENT | WATER
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 01/2017, Volume 58, Issue 2, pp. 168 - 171
4 -Chromenes were synthesized from 2-bromobenzylidenemalonates and 1,3-dicarbonyls under mild and simple reaction conditions copper-catalysed domino reactions...
Michael addition | Chromenes | Copper-catalysed domino reaction | Ullmann-type coupling | C(aryl)–O bond formation | FUNCTIONALIZED 4H-CHROMENES | PHOTOCHROMISM | CHEMISTRY, ORGANIC | C(aryL)-O bond formation | KETONES | COUPLING REACTIONS | SELECTIVE SYNTHESIS | EFFICIENT | DERIVATIVES | CYCLIZATION | Copper
Michael addition | Chromenes | Copper-catalysed domino reaction | Ullmann-type coupling | C(aryl)–O bond formation | FUNCTIONALIZED 4H-CHROMENES | PHOTOCHROMISM | CHEMISTRY, ORGANIC | C(aryL)-O bond formation | KETONES | COUPLING REACTIONS | SELECTIVE SYNTHESIS | EFFICIENT | DERIVATIVES | CYCLIZATION | Copper
Journal Article
RSC ADVANCES, ISSN 2046-2069, 2014, Volume 4, Issue 97, pp. 54168 - 54174
Different types of multicomponent reactions (MCRs) are reported using Bi2O3, BiVO4, and Bi2WO6 (nanoparticle) as heterogeneous catalysts. Among these, Bi2WO6...
BISMUTH(III) COMPOUNDS | ORGANIC-SYNTHESIS | SOLVENT-FREE CONDITIONS | MANNICH-TYPE REACTION | ENANTIOSELECTIVE SYNTHESIS | HANTZSCH 1,4-DIHYDROPYRIDINES | 3-COMPONENT REACTION | EFFICIENT SYNTHESIS | DENSELY FUNCTIONALIZED 4H-CHROMENES | OXIDATIVE AROMATIZATION | CHEMISTRY, MULTIDISCIPLINARY
BISMUTH(III) COMPOUNDS | ORGANIC-SYNTHESIS | SOLVENT-FREE CONDITIONS | MANNICH-TYPE REACTION | ENANTIOSELECTIVE SYNTHESIS | HANTZSCH 1,4-DIHYDROPYRIDINES | 3-COMPONENT REACTION | EFFICIENT SYNTHESIS | DENSELY FUNCTIONALIZED 4H-CHROMENES | OXIDATIVE AROMATIZATION | CHEMISTRY, MULTIDISCIPLINARY
Journal Article
The Chemical Record, ISSN 1527-8999, 02/2017, Volume 17, Issue 2, pp. 142 - 183
Compounds containing oxygen, nitrogen, or sulfur atoms inside the rings are attracting much attention and interest due to their biological importance. In...
multicomponent reactions | bifunctional building blocks | structure-activity relationships | heterocycles | green chemistry | HIGHLY ENANTIOSELECTIVE SYNTHESIS | SOLVENT-FREE CONDITIONS | ONE-POT SYNTHESIS | LARGE-SCALE SYNTHESIS | ORGANOCATALYTIC ASYMMETRIC-SYNTHESIS | N-SUBSTITUTED ISOINDOLINONES | CHEMISTRY, MULTIDISCIPLINARY | CATALYST-FREE SYNTHESIS | RING-FUSED AMINALS | DOMINO REACTION SYNTHESIS | DENSELY FUNCTIONALIZED 4H-CHROMENES | Green design
multicomponent reactions | bifunctional building blocks | structure-activity relationships | heterocycles | green chemistry | HIGHLY ENANTIOSELECTIVE SYNTHESIS | SOLVENT-FREE CONDITIONS | ONE-POT SYNTHESIS | LARGE-SCALE SYNTHESIS | ORGANOCATALYTIC ASYMMETRIC-SYNTHESIS | N-SUBSTITUTED ISOINDOLINONES | CHEMISTRY, MULTIDISCIPLINARY | CATALYST-FREE SYNTHESIS | RING-FUSED AMINALS | DOMINO REACTION SYNTHESIS | DENSELY FUNCTIONALIZED 4H-CHROMENES | Green design
Journal Article