Regioselective addition reactions of silyl enolates to a, b-unsaturated aldehyde and its acetal catalyzed by MgI2 etherate give aldol adducts (1, 2-addition) preferentially over Michael adducts (1, 4-addition). This ...Regioselective addition reactions of silyl enolates to a, b-unsaturated aldehyde and its acetal catalyzed by MgI2 etherate give aldol adducts (1, 2-addition) preferentially over Michael adducts (1, 4-addition). This unique regioselectivity is distinctly different with other Lewis acidic promoters and may be attributed to the high oxyphilicity of IMg+.展开更多
The nucleophilic addition of Ti(IV) enolate derived from methyl aryl ketones to α, β–unsaturated compounds was found to be highly selective to give 1, 2 addition products.
Summary of main observation and conclusion A general and efficient protocol to synthesize substituted olefins from carbonyl compounds via nickel catalyzed C-O activation of enolates was developed.Besides ketones,aldeh...Summary of main observation and conclusion A general and efficient protocol to synthesize substituted olefins from carbonyl compounds via nickel catalyzed C-O activation of enolates was developed.Besides ketones,aldehydes were also suitable substrates for the presented catalytic system to produce di-or tri-substituted olefins.It is worth noting that this approach exhibited good tolerance to highly reactive tertiary alcohols,which could not survive in other reported routes for converting carbonyl compounds to olefins.This method also showed good regio-and stereo-selectivity for olefin products.Preliminary mechanistic studies indicated that the reaction was accomplished through nickel catalyzed C-O activation of enolates,thus offering helpful contribution to current enol chemistry.展开更多
Diphenyl diamine-based phosphonyl imines attached by the N-isopropyl group in the auxiliary have been synthesized in good yields under convenient reaction conditions.These new chiral N-phosphonyl imines can react with...Diphenyl diamine-based phosphonyl imines attached by the N-isopropyl group in the auxiliary have been synthesized in good yields under convenient reaction conditions.These new chiral N-phosphonyl imines can react with glycine enolate smoothly to give chiral α-β diamino esters in good yields(72%-90%) and up to excellent diastereoselectivity(】99:1 dr).By treatment with HBr,the chiral auxiliary can be readily removed.The absolute structure has been unambiguously determined by converting a product to a known sample.展开更多
Silyl enol ethers are often obtained when the lithium enolates are trapped with chlorosilanes.Herein,we report a general method for the regio-and diasteroselective C-silylation of enolate enabled by theβ-boronyl grou...Silyl enol ethers are often obtained when the lithium enolates are trapped with chlorosilanes.Herein,we report a general method for the regio-and diasteroselective C-silylation of enolate enabled by theβ-boronyl group.The formation of five-membered chelation intermediate is key to the C-selective silylation and anti-selectivity.The operationally simple protocol provides a general and predictable access to theα-silylated esters.The synthetic versatility of the boron-silicon bifunctional products was demonstrated by down-stream transformations.展开更多
A rhodium(Ⅲ)-catalyzed hydrosilylation/cyclization reaction of cyclohexadienone-tetheredα,β-unsaturated aldehydes(1,6-dienes)with triethylsilane is described,providing a series of cishydrobenzofurans,cis-hydroindol...A rhodium(Ⅲ)-catalyzed hydrosilylation/cyclization reaction of cyclohexadienone-tetheredα,β-unsaturated aldehydes(1,6-dienes)with triethylsilane is described,providing a series of cishydrobenzofurans,cis-hydroindoles,and cishydroindenes bearing silyl enol ether in good to excellent yields and excellent stereoselectivities.Additionally,the versatility of this method was demonstrated through a gram-scale experiment and various downstream transformations,highlighting its utility.展开更多
An efficient protocol for the synthesis of asymmetric 1,3-diketones was reported through diacylation of1,1-diborylalkanes using two different acyl sources.In this transfo rmation,an enolate boron species was initially...An efficient protocol for the synthesis of asymmetric 1,3-diketones was reported through diacylation of1,1-diborylalkanes using two different acyl sources.In this transfo rmation,an enolate boron species was initially formed by introducing an acyl group,then it was trapped by another acyl group to form 1,3-diketone.This method not only provided the gateway to obtain a series of 1,3-diketones,but also afforded an operationally simple and efficient access to pyrazoles and isoxazoles.展开更多
The semi-hydrogenation of alkynols to enols is a crucial process in the production of pharmaceuticals,agrochemicals,fragrances,and flavors that involves a complex set of parallel and consecutive isomerization and hydr...The semi-hydrogenation of alkynols to enols is a crucial process in the production of pharmaceuticals,agrochemicals,fragrances,and flavors that involves a complex set of parallel and consecutive isomerization and hydrogenation reactions and proceeds via several key intermediates.In view of the industrial importance of large-scale enol production through alkynol hydrogenation,various noble and non-noble metal(e.g.,Ni and Pd)-based catalysts promoting this transformation have been developed.This paper reviews the design of highly selective catalysts for the semi-hydrogenation of alkynols,focusing on the role of additives,second metals,catalyst supports,and reaction conditions and combining catalytic reaction kinetics with theoretical calculations to establish the reaction mechanism and the decisive factors for boosting selectivity.Finally,a strategy for designing highly efficient and selective catalysts based on the characteristics of aqueous-phase alkynol hydrogenation is proposed.展开更多
Spirotetramat metabolizes to its active enol form in the plant. We described here a photocaged pesticide delivery system that can release insecticidal spirotetramat enol form upon light irradiation. Covalently linking...Spirotetramat metabolizes to its active enol form in the plant. We described here a photocaged pesticide delivery system that can release insecticidal spirotetramat enol form upon light irradiation. Covalently linking spirotetramat-enol with photoresponsive coumarin generated the caged insecticide. The photophysical and photochemical properties, deprotection photolysis and insecticidal activities of the caged spirotetramat enol were studied. This light-triggered system can undergo cleavage to release free spirotetramat enol form at the presence of blue light （420 nm） or sunlight, Bioassays indicated that the triggered molecule has no obvious insecticidal activity against Aphis craccivora Koch at dark and could be activated by light to release the insecticidal ingredients, which provides precise control over insecticide delivery.展开更多
The influence of SO2 on the performance of Ag-Pd/Al2O3 for the selective catalytic reduction （SCR） of NOx with C2H5OH was investigated experimentally. The activity test results suggest that Ag-Pd/Al2O3 shows a small...The influence of SO2 on the performance of Ag-Pd/Al2O3 for the selective catalytic reduction （SCR） of NOx with C2H5OH was investigated experimentally. The activity test results suggest that Ag-Pd/Al2O3 shows a small activity loss in the presence of SO2 when using C2H5OH as a reductant. In situ DRIFTS spectra show that the activity loss originates from the formation of surface sulphate species on the Ag-Pd/Al2O3. The surface sulphate species formation inhibits the formation of nitrate, whereas hardly changes the partial oxidation of C2H5OH. Compared with the NOx reduction by C3H6, an obvious suppression of the surface sulphate species formation was observed by DRIFTS experiment when using C2H5OH as a reductant. This phenomenon reveals the better catalytic performance and strong SO2 tolerance of Ag-Pd/Al2O3-C2H50H system.展开更多
α, β-unsaturated esters were often synthesized from aldehydes and esters in the presence of strong organic base that was very sensitive to air and moisture via aldol reaction. Trioxane was very useful C1 resource, h...α, β-unsaturated esters were often synthesized from aldehydes and esters in the presence of strong organic base that was very sensitive to air and moisture via aldol reaction. Trioxane was very useful C1 resource, however, the decomposition of it was always the challenging problem that facing researchers. Herein, a novel synthetic methodology for α, β-unsaturated ester preparation from trioxane and ester with mild catalysis of generated ammonium trifluoromethanesulfonate ionic liquid. The enolization of ester as well as the decomposition of trioxane could proceed easily in the presence of boryl trifluoromethanesulfonate and amine at 20–25℃. Then the enolate and decomposed formaldehyde occurs aldol reaction to form α, β-unsaturated ester. With this strategy, the yield and selectivity of product from various substrates including aliphatic esters,lactones and thioester could reach up to 85.2% and 90.1%.展开更多
Objective: Hypoxia is an important feature of pancreatic ductal adenocarcinoma(PDAC). Previously, we found that hypoxia promotes ENO1 expression and PDAC invasion. However, the underlying molecular mechanism was remai...Objective: Hypoxia is an important feature of pancreatic ductal adenocarcinoma(PDAC). Previously, we found that hypoxia promotes ENO1 expression and PDAC invasion. However, the underlying molecular mechanism was remains unclear.Methods: The relationship between ENO1 expression and clinicopathological characteristics was analyzed in 84 patients with PADC. The effects of CoCl2-induced hypoxia and ENO1 downregulation on the apoptosis, invasion, and proliferation of PDAC cells were evaluated in vitro and in vivo. Hypoxia-and ENO1-induced gene expression was analyzed by transcriptomic sequencing.Results: The prognosis of PDAC with high ENO1 expression was poor(P < 0.05). High ENO1 expression was closely associated with histological differentiation and tumor invasion in 84 PDAC cases(P < 0.05). Hypoxia increased ENO1 expression in PDAC and promoted its migration and invasion. Apoptotic cells and the apoptosis marker caspase-3 in the CoCl_(2)-treated ENO1-sh group were significantly elevated(P < 0.05). Transcriptomic sequencing indicated that CoCl_(2)-induced PDAC cells initiated MAPK signaling. Under hypoxic conditions, PDAC cells upregulated ENO1 expression, thereby accelerating ERK phosphorylation and inhibiting apoptosis(P < 0.05). Consistent results were also observed in a PDAC-bearing mouse hindlimb ischemia model.Conclusions: Hypoxia-induced ENO1 expression promotes ERK phosphorylation and inhibits apoptosis, thus leading to PDAC survival and invasion. These results suggest that ENO1 is a potential therapeutic target for PDAC.展开更多
A facile and highly efficient approach for selective O-difluoromethylation of 1,3-diones by recently developed bench-stable S-(difluoromethyl)sulfonium salt was described.And a broad range of difluoromthyl enol ethers...A facile and highly efficient approach for selective O-difluoromethylation of 1,3-diones by recently developed bench-stable S-(difluoromethyl)sulfonium salt was described.And a broad range of difluoromthyl enol ethers were readily accessed in good to excellent yields under mild reaction conditions.Mechanistic studies revealed that the O-difluoromethylation reaction proceeds mainly via a difluorocarbene pathway.展开更多
The tetrahydroquinoline moiety is a structural feature of many natural products. By using a domino reaction of aromatic amines and cyclic enol ethers catalyzed by zirconyl chloride in water, various tetrahydroquinolin...The tetrahydroquinoline moiety is a structural feature of many natural products. By using a domino reaction of aromatic amines and cyclic enol ethers catalyzed by zirconyl chloride in water, various tetrahydroquinoline derivatives were synthesized efficiently. Most cyclized products showed cis selectivity. The cis selectivity was tentatively rationalized due to chelation control in water.展开更多
A domino reaction of anilines with cyclic and acyclic enol ethers induced by catalytic amounts of TBPA^（·＋）（5 mol%） was investigated and a series of 2,4-disubstituted-1,2,3,4-tetrahydroquinolines were synthe...A domino reaction of anilines with cyclic and acyclic enol ethers induced by catalytic amounts of TBPA^（·＋）（5 mol%） was investigated and a series of 2,4-disubstituted-1,2,3,4-tetrahydroquinolines were synthesized.Different from cyclic enol ethers, when acyclic enol ethers were used in the reaction,they serve as surrogates of acetaldehyde,producing a series of 2-methyl-4- anilino-1,2,3,4-tetrahydroquinolines.A single electron transfer mechanism was proposed to rationalize the products formation.展开更多
K5CoW12O40 was used as a highly effective catalyst for the benzylation of 1,3-dicarbonyl compounds, β-Keto enol ethers were obtained when cyclic 1,3-dicarbonyl compounds used in this conditions instead of linear ones...K5CoW12O40 was used as a highly effective catalyst for the benzylation of 1,3-dicarbonyl compounds, β-Keto enol ethers were obtained when cyclic 1,3-dicarbonyl compounds used in this conditions instead of linear ones. The present methodology offers a practical, simple, mild, environmentally friendly, and time-saving method for etherification. Very low loading of catalyst, ease of workup, ease of handling, and reusability of catalyst are other advantages of this catalyst.展开更多
A novel oscillating chemical reaction using ninhydrin as a single organic substrate was represented in this paper. It distinguished from the classically catalyzed BZ oscillating chemical reaction due to there was no a...A novel oscillating chemical reaction using ninhydrin as a single organic substrate was represented in this paper. It distinguished from the classically catalyzed BZ oscillating chemical reaction due to there was no active methene （CH2=） and/or enol structure in the ninhydrin molecule, which served as single organic substrate. This suggested that the substrates used in catalyzed BZ reaction were not always the organic compounds containing active methene （CH2=） and/or enol structure and bromination process in this kind of catalyzed chemical oscillating reaction was not also necessary.展开更多
The title compound (p-methylphenylbis(4, 4-dimethyl-6-hydroxycyclohexene-1-one-2-yl)methane) has been synthesized by the reaction of 4-methylbenzaldehyde and 5, 5-dimethyl-1, 3-cyclohexanedione in N,N-dimethylformamid...The title compound (p-methylphenylbis(4, 4-dimethyl-6-hydroxycyclohexene-1-one-2-yl)methane) has been synthesized by the reaction of 4-methylbenzaldehyde and 5, 5-dimethyl-1, 3-cyclohexanedione in N,N-dimethylformamide. Its structure was determined by single crystal X-ray diffraction. The Crystal is monoclinic, space group P21/a, a=0. 9304 (2)nm, b=1. 1754 (2)nm, c=2. 0134 (4)nm, β=102. 40(2)°, Mr= 382. 50, V=2. 1505 (7)nm3, Dc = 1. 181g/cm3, Z=4, μ(MoKα) = 0. 79cm-1, F(000) = 856.The structure was solved by direct methods, and refined by full-matris least-Squares method to a final R =0. 042 and Rw = 0. 045. The crystal structure shows that there are two conjugated enol form in the molecule.展开更多
基金We are grateful for the financial supports from the National Outstanding Youth Fund No.29925204)the Foundation for University Key Teacher by the Ministry of Education of Chinaa Visiting Fund of the National Laboratory of Applied Organic Chemistry.
文摘Regioselective addition reactions of silyl enolates to a, b-unsaturated aldehyde and its acetal catalyzed by MgI2 etherate give aldol adducts (1, 2-addition) preferentially over Michael adducts (1, 4-addition). This unique regioselectivity is distinctly different with other Lewis acidic promoters and may be attributed to the high oxyphilicity of IMg+.
文摘The nucleophilic addition of Ti(IV) enolate derived from methyl aryl ketones to α, β–unsaturated compounds was found to be highly selective to give 1, 2 addition products.
文摘Summary of main observation and conclusion A general and efficient protocol to synthesize substituted olefins from carbonyl compounds via nickel catalyzed C-O activation of enolates was developed.Besides ketones,aldehydes were also suitable substrates for the presented catalytic system to produce di-or tri-substituted olefins.It is worth noting that this approach exhibited good tolerance to highly reactive tertiary alcohols,which could not survive in other reported routes for converting carbonyl compounds to olefins.This method also showed good regio-and stereo-selectivity for olefin products.Preliminary mechanistic studies indicated that the reaction was accomplished through nickel catalyzed C-O activation of enolates,thus offering helpful contribution to current enol chemistry.
基金supported by the National Institutes of Health (Grant Nos.1 RO3 DA026960-01)Robert Welch Foundation (Grant No.D-1361)
文摘Diphenyl diamine-based phosphonyl imines attached by the N-isopropyl group in the auxiliary have been synthesized in good yields under convenient reaction conditions.These new chiral N-phosphonyl imines can react with glycine enolate smoothly to give chiral α-β diamino esters in good yields(72%-90%) and up to excellent diastereoselectivity(】99:1 dr).By treatment with HBr,the chiral auxiliary can be readily removed.The absolute structure has been unambiguously determined by converting a product to a known sample.
基金Financial support was provided by the National Natural Science Foundation of China(Nos.22001210 and 21971202)the Natural Science Basic Research Plan of Shaanxi Province(2020JC-08)。
文摘Silyl enol ethers are often obtained when the lithium enolates are trapped with chlorosilanes.Herein,we report a general method for the regio-and diasteroselective C-silylation of enolate enabled by theβ-boronyl group.The formation of five-membered chelation intermediate is key to the C-selective silylation and anti-selectivity.The operationally simple protocol provides a general and predictable access to theα-silylated esters.The synthetic versatility of the boron-silicon bifunctional products was demonstrated by down-stream transformations.
基金financial support from the National Key R&D Program of China(No.2022YFF1202600)the National Natural Science Foundation of China(Nos.22001172,22071155,and22371188)+4 种基金the Science and Technology Commission of Shanghai Municipality(Nos.20XD1403600 and 20400750300)the Shanghai Municipal Education Commission(No.2019-01-07-00-10-E00072)the Innovation Team and Talents Cultivation Program of National Administration of Traditional Chinese Medicine(No.ZYYCXTD-202004)the Shanghai Municipal Health Commission/Shanghai Municipal Administration of Traditional Chinese Medicine[No.ZY(2021-2023)-0501]Organizational Key R&D Program of SHUTCM(No.2023YZZ01)。
文摘A rhodium(Ⅲ)-catalyzed hydrosilylation/cyclization reaction of cyclohexadienone-tetheredα,β-unsaturated aldehydes(1,6-dienes)with triethylsilane is described,providing a series of cishydrobenzofurans,cis-hydroindoles,and cishydroindenes bearing silyl enol ether in good to excellent yields and excellent stereoselectivities.Additionally,the versatility of this method was demonstrated through a gram-scale experiment and various downstream transformations,highlighting its utility.
基金the National Natural Science Foundation of China(Nos.91745110,21673261,21603245,21703265,21872156,21802150,21773210 and 21603190)Natural Science Foundation of Jiangsu Province(Nos.BK20190002,BK20181194 and BK20180247)+1 种基金Support from the Young Elite Scientist Sponsorship Program by CAST(No.YESS20170217)the Youth Innovation Promotion Association CAS(No.2018458)。
文摘An efficient protocol for the synthesis of asymmetric 1,3-diketones was reported through diacylation of1,1-diborylalkanes using two different acyl sources.In this transfo rmation,an enolate boron species was initially formed by introducing an acyl group,then it was trapped by another acyl group to form 1,3-diketone.This method not only provided the gateway to obtain a series of 1,3-diketones,but also afforded an operationally simple and efficient access to pyrazoles and isoxazoles.
文摘The semi-hydrogenation of alkynols to enols is a crucial process in the production of pharmaceuticals,agrochemicals,fragrances,and flavors that involves a complex set of parallel and consecutive isomerization and hydrogenation reactions and proceeds via several key intermediates.In view of the industrial importance of large-scale enol production through alkynol hydrogenation,various noble and non-noble metal(e.g.,Ni and Pd)-based catalysts promoting this transformation have been developed.This paper reviews the design of highly selective catalysts for the semi-hydrogenation of alkynols,focusing on the role of additives,second metals,catalyst supports,and reaction conditions and combining catalytic reaction kinetics with theoretical calculations to establish the reaction mechanism and the decisive factors for boosting selectivity.Finally,a strategy for designing highly efficient and selective catalysts based on the characteristics of aqueous-phase alkynol hydrogenation is proposed.
基金financially supported by the National Natural Science Foundation of China (Nos. 21472046, 21372079)Science and Technology Commission of Shanghai Municipality (No. 16391902300)the Fundamental Research Funds for the Central Universities (No. 222201718004)
文摘Spirotetramat metabolizes to its active enol form in the plant. We described here a photocaged pesticide delivery system that can release insecticidal spirotetramat enol form upon light irradiation. Covalently linking spirotetramat-enol with photoresponsive coumarin generated the caged insecticide. The photophysical and photochemical properties, deprotection photolysis and insecticidal activities of the caged spirotetramat enol were studied. This light-triggered system can undergo cleavage to release free spirotetramat enol form at the presence of blue light （420 nm） or sunlight, Bioassays indicated that the triggered molecule has no obvious insecticidal activity against Aphis craccivora Koch at dark and could be activated by light to release the insecticidal ingredients, which provides precise control over insecticide delivery.
基金The Key Program of the National Natural Science Foundation of China (No. 20437010) and the National Science Fund forDistinguished Young Scholars of China (No. 20425722)
文摘The influence of SO2 on the performance of Ag-Pd/Al2O3 for the selective catalytic reduction （SCR） of NOx with C2H5OH was investigated experimentally. The activity test results suggest that Ag-Pd/Al2O3 shows a small activity loss in the presence of SO2 when using C2H5OH as a reductant. In situ DRIFTS spectra show that the activity loss originates from the formation of surface sulphate species on the Ag-Pd/Al2O3. The surface sulphate species formation inhibits the formation of nitrate, whereas hardly changes the partial oxidation of C2H5OH. Compared with the NOx reduction by C3H6, an obvious suppression of the surface sulphate species formation was observed by DRIFTS experiment when using C2H5OH as a reductant. This phenomenon reveals the better catalytic performance and strong SO2 tolerance of Ag-Pd/Al2O3-C2H50H system.
基金the National Key Projects for Fundamental Research and Development of China (No. 2016YFB0601303)the Key Research Program of Frontier Sciences (No. QYZDBSSW-SLH022)+3 种基金the International Cooperation and Exchange of the National Natural Science Foundation of China (No. 51561145020)Key Program of National Natural Science Foundation of China (No. 91434203)National Natural Science Foundation of China (No. 21676270)NSFC-Key Projects of Shanxi Coal Based Low Carbon Joint Fundation (No. U1610222)
文摘α, β-unsaturated esters were often synthesized from aldehydes and esters in the presence of strong organic base that was very sensitive to air and moisture via aldol reaction. Trioxane was very useful C1 resource, however, the decomposition of it was always the challenging problem that facing researchers. Herein, a novel synthetic methodology for α, β-unsaturated ester preparation from trioxane and ester with mild catalysis of generated ammonium trifluoromethanesulfonate ionic liquid. The enolization of ester as well as the decomposition of trioxane could proceed easily in the presence of boryl trifluoromethanesulfonate and amine at 20–25℃. Then the enolate and decomposed formaldehyde occurs aldol reaction to form α, β-unsaturated ester. With this strategy, the yield and selectivity of product from various substrates including aliphatic esters,lactones and thioester could reach up to 85.2% and 90.1%.
基金supported by grants from the National Natural Science Key Foundation of China(Grant No.82030092).
文摘Objective: Hypoxia is an important feature of pancreatic ductal adenocarcinoma(PDAC). Previously, we found that hypoxia promotes ENO1 expression and PDAC invasion. However, the underlying molecular mechanism was remains unclear.Methods: The relationship between ENO1 expression and clinicopathological characteristics was analyzed in 84 patients with PADC. The effects of CoCl2-induced hypoxia and ENO1 downregulation on the apoptosis, invasion, and proliferation of PDAC cells were evaluated in vitro and in vivo. Hypoxia-and ENO1-induced gene expression was analyzed by transcriptomic sequencing.Results: The prognosis of PDAC with high ENO1 expression was poor(P < 0.05). High ENO1 expression was closely associated with histological differentiation and tumor invasion in 84 PDAC cases(P < 0.05). Hypoxia increased ENO1 expression in PDAC and promoted its migration and invasion. Apoptotic cells and the apoptosis marker caspase-3 in the CoCl_(2)-treated ENO1-sh group were significantly elevated(P < 0.05). Transcriptomic sequencing indicated that CoCl_(2)-induced PDAC cells initiated MAPK signaling. Under hypoxic conditions, PDAC cells upregulated ENO1 expression, thereby accelerating ERK phosphorylation and inhibiting apoptosis(P < 0.05). Consistent results were also observed in a PDAC-bearing mouse hindlimb ischemia model.Conclusions: Hypoxia-induced ENO1 expression promotes ERK phosphorylation and inhibits apoptosis, thus leading to PDAC survival and invasion. These results suggest that ENO1 is a potential therapeutic target for PDAC.
基金supported by the Science and Technology Foundation of Shenzhen, Shenzhen Science and Technology Innovation Committee (No. JCYJ20170818143001461)
文摘A facile and highly efficient approach for selective O-difluoromethylation of 1,3-diones by recently developed bench-stable S-(difluoromethyl)sulfonium salt was described.And a broad range of difluoromthyl enol ethers were readily accessed in good to excellent yields under mild reaction conditions.Mechanistic studies revealed that the O-difluoromethylation reaction proceeds mainly via a difluorocarbene pathway.
文摘The tetrahydroquinoline moiety is a structural feature of many natural products. By using a domino reaction of aromatic amines and cyclic enol ethers catalyzed by zirconyl chloride in water, various tetrahydroquinoline derivatives were synthesized efficiently. Most cyclized products showed cis selectivity. The cis selectivity was tentatively rationalized due to chelation control in water.
基金We thank NSFC(No.21002079)Project(No.20096203120002)supported by the Ministry of Education of the People's Republic of China.We also thank the third Knowledge and Technological Innovation Project(No.NWNUKJCXGC -03-75 and NWNU-KJCXGC-03-64) of Northwest Normal University for supporting our research
文摘A domino reaction of anilines with cyclic and acyclic enol ethers induced by catalytic amounts of TBPA^（·＋）（5 mol%） was investigated and a series of 2,4-disubstituted-1,2,3,4-tetrahydroquinolines were synthesized.Different from cyclic enol ethers, when acyclic enol ethers were used in the reaction,they serve as surrogates of acetaldehyde,producing a series of 2-methyl-4- anilino-1,2,3,4-tetrahydroquinolines.A single electron transfer mechanism was proposed to rationalize the products formation.
基金the Razi University Research Council for support of this work
文摘K5CoW12O40 was used as a highly effective catalyst for the benzylation of 1,3-dicarbonyl compounds, β-Keto enol ethers were obtained when cyclic 1,3-dicarbonyl compounds used in this conditions instead of linear ones. The present methodology offers a practical, simple, mild, environmentally friendly, and time-saving method for etherification. Very low loading of catalyst, ease of workup, ease of handling, and reusability of catalyst are other advantages of this catalyst.
文摘A novel oscillating chemical reaction using ninhydrin as a single organic substrate was represented in this paper. It distinguished from the classically catalyzed BZ oscillating chemical reaction due to there was no active methene （CH2=） and/or enol structure in the ninhydrin molecule, which served as single organic substrate. This suggested that the substrates used in catalyzed BZ reaction were not always the organic compounds containing active methene （CH2=） and/or enol structure and bromination process in this kind of catalyzed chemical oscillating reaction was not also necessary.
文摘The title compound (p-methylphenylbis(4, 4-dimethyl-6-hydroxycyclohexene-1-one-2-yl)methane) has been synthesized by the reaction of 4-methylbenzaldehyde and 5, 5-dimethyl-1, 3-cyclohexanedione in N,N-dimethylformamide. Its structure was determined by single crystal X-ray diffraction. The Crystal is monoclinic, space group P21/a, a=0. 9304 (2)nm, b=1. 1754 (2)nm, c=2. 0134 (4)nm, β=102. 40(2)°, Mr= 382. 50, V=2. 1505 (7)nm3, Dc = 1. 181g/cm3, Z=4, μ(MoKα) = 0. 79cm-1, F(000) = 856.The structure was solved by direct methods, and refined by full-matris least-Squares method to a final R =0. 042 and Rw = 0. 045. The crystal structure shows that there are two conjugated enol form in the molecule.
