共查询到20条相似文献,搜索用时 46 毫秒
1.
Recently,muchefforthasbeenmadeinthedevelopmentofgenerallyapplicableorganicsynthesisof5hydroxy2(5H)furanone1duetoitsessentialstructureentityinthesynthesisofsomebiologicallyactivenaturalproductsanditsapplicationasausefulintermediateinorganicsynthesis[1—3].Co… 相似文献
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Ingleson MJ Barrio JP Bacsa J Dickinson C Park H Rosseinsky MJ 《Chemical communications (Cambridge, England)》2008,(11):1287-1289
Protonation of chiral porous materials introduces a Br?nsted acid centre, the structure of which is unique to the heterogeneous phase requiring pore wall confinement for stable isolation. 相似文献
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SHI Ji-Cheng WEN Ting-Bin WU Da-Xu LU Ge-Tan HONG Mao-ChunLIU Qiu-Tian KANG Bei-ShengState Key Laboratory of Structural Chemistry Fujian Institute of Research on the Structure of Matter Chinese Academy of Sciences Fuzhou Fujian ChinaWANG Han-Qing LU Shi-JieLanzhou Institute of Chemical Physics Chinese Academy of Sciences Lanzhou Gansu China 《中国化学》1996,14(5):454-461
Methyl 3-deoxy-3-(diphenylphosphino)-4,6-O-benzylidene-α-D-altropyranoside (1) and methyl 2-deoxy-2-(diphenylphosphino)-4,6-O-benzylidene-α-D-altropyranoside (2) were prepared from methyl 2,3-anhydro-4,6-O-benzylidene-O-D-mannopyranoside and methyl 2,3-anhydro-4,6-O-benzyl-idene-α-D-allopyranoside,respectively,via regioselective and stcreospecific ring-opening reactions in high yields.Compounds 1 and 2 were oxidized to give the corresponding phosphine oxides (3 and 4). 相似文献
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Bo Tang Wei Wang Huipeng Hou Yiquan Liu Zongkun Liu Lina Geng Liquan Sun Aiqin Luo 《中国化学快报》2022,33(2):898-902
Chiral covalent organic frameworks(CCOFs) featuring chirality, stability, and good porosity have attracted a considerable amount of attention due to their important applications, such as asymmetric catalysis, chiral separation, and chiral recognition. In this study, a β-cyclodextrin(β-CD) covalent organic framework(β-CD-COF) diluted with polysiloxane OV-1701 was explored as a novel chiral stationary phase(CSP) for gas chromatography(GC) separation of racemates. The β-CD-COF coated capillary colu... 相似文献
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Pardo C Sesmilo E Gutiérrez-Puebla E Monge A Elguero J Fruchier A 《The Journal of organic chemistry》2001,66(5):1607-1611
A convenient synthesis of 5alpha,8alpha,14alpha,17alpha-5,17:8,14-dimethano-5,8,14,17-tetraaza-5,6,7,8,13,14,17,18-octahydrodibenzo[e,e']benzo[1,2-a:3,4-a']dicyclooctene derivatives is described, and the compounds have been fully characterized by NMR; in some cases, the molecular structure has been determined by X-ray crystallography. These compounds represent the first examples of a new class of molecular tweezers. 相似文献
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Highly diastereoselective and enantioselective catalytic capture of chiral zinc enolates using nitroolefins as electrophiles is described. The tandem products γ-nitro ketones were obtained in good yields with high diastereoselectivities and enantioselectivities. The γ-nitro ketones were readily hydrogenated to the optically enriched and diastereomerically pure chiral pyrrolidines with four contiguous stereocentres under mild conditions. 相似文献
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A highly reactive and acidic chiral Br?nsted acid catalyst, chiral N-triflyl phosphoramide, was developed. Highly enantioselective Diels-Alder reaction of alpha,beta-unsaturated ketone with silyloxydiene was demonstrated using this chiral Br?nsted acid catalyst. 相似文献
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Okano K Taguchi M Fujiki M Yamashita T 《Angewandte Chemie (International ed. in English)》2011,50(52):12474-12477
Sucked into the vortex: Hydrogels with embedded Rhodamine?B dye showed stir-induced circularly polarized luminescence (CPL; see picture), the sense of which can be controlled by switching the stir direction from clockwise (CW) to counterclockwise (CCW) with slow cooling from the sol to gel states. The chiral alignment of the dye was erased by heating the sample above the gel-sol transition temperature. 相似文献
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DING Zong-Biao CHENG Ke-Jun WU Shi-HuiDepartment of Chemistry Fudan University Shanghai China 《中国化学》1996,14(6):561-564
A new type of chiral 1,1'-binaphthol(BINOL) derived samarium complex, preparedfrom (R)- or (S)-BINOL and SmCl3, serves as an enantioselective catalyst for the Meerwein-Ponndorf-Verley (MPV) reduction in the presence of Molecular Sieves 4A(MS 4A). Moderate enantioselectivity was obtained. Kinetic studies show slight decrease of the enantiomeric excess with the conversion. 相似文献
11.
Baeck Kyoung Lee Hwan Geun Choi Eun Joo Roh Won Koo Lee Taebo Sim 《Tetrahedron letters》2013,54(6):553-556
An efficient synthesis of (?)-8-epi-swainsonine, starting from a commercially available 1-(R)-α-methylbenzylaziridine-2-methanol, was developed. The synthetic route utilizes stereocontrolled Sharpless asymmetric dihydroxylation governed by AD-mix-β followed by an aziridine ring opening-cyclization sequence to generate the five membered N-heterocyclic ring system present in the bicyclic target. A subsequent stereoselective allylation and piperidine ring forming cyclization then produced a precursor that was converted into (?)-8-epi-swainsonine. 相似文献
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《Tetrahedron: Asymmetry》2001,12(6):915-921
The regio- and stereochemistry of the alkylation of dienediolates from unsaturated carboxylic acids with benzylic halides, which often results in mixtures of isomers, can be controlled by means of changes in the lithium amide, allowing the α-regioisomer to be obtained as the major diastereoisomer. In addition, when chiral amines are used, moderate enantiomeric excesses can be attained. 相似文献
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《Tetrahedron: Asymmetry》2000,11(16):3283-3292
Threo-β-hydroxy-l-glutamic acid derivatives with different carboxylic acid protecting groups were stereoselectively prepared from a chiral aziridine-2-carboxylate using an aldol reaction, stereoselective ketone reduction, and aziridine ring transformation. 相似文献
16.
The title complex l-[CuⅡ4(Hvap)2(vap)2(MeOH)2](CIO4)2 1 has been synthesized and characterized by EA. IR,TGA,solid-state CD spectra and X-ray single-crystal analyses(l-H2vap’.a Schiff base ligand derived from the condensation of o-vanillin and l-2-amino-3-phenyl-l-propanol).Complex 1 crystallizes in monoclinic system,chiral space group P21 with a =10.4257(18).b = 21.695(4),c = 15.721(3)A,β= 94.443(3).V= 3545.1(11) 3,Z=2,Cu4C70H78N4O22Cl2.Mr= 1652.42,Dc= 1.548 g/cm3, F(000)= 1704 andμ(MoKα) = 1.338 mm-1.The final R = 0.0682 and wR = 0.1420 for 6170 observed reflections with I > 2σ(I) and R = 0.1775 and wR = 0.1830 for all data.The structure of complex 1 contains a boat-shaped(Cu4O4} motif.The solid-state CD spectra confirm the chiral nature of complex 1. 相似文献
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The pseudo C(2) symmetric trans diphenyl oxazoline group acts as an effective chiral auxiliary in the 8π, 6π tandem electrocyclization of a substituted tetraene 1-carboxylic acid. Assignment of absolute stereochemistry to the [4.2.0] bicyclooctadiene product supports a model in which both s-cis and s-trans conformations favor the transition states with the same helical twist. This assignment prefaces the development of analogs of SNF4435 C and D. These natural products demonstrate activity as androgen receptor antagonists and as multidrug resistance (mdr) reversal agents. 相似文献
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《Tetrahedron letters》1988,29(46):5881-5884
The X-ray structural analysis of the SnCl4 adduct of 2-benzyloxy-3- pentanone shows for the first time the existence and precise geometry of a monomeric chiral α-alkoxy ketone chelate. 相似文献
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Shunsuke Kotani Masaya Ito Hirono Nozaki Masaharu Sugiura Masamichi Ogasawara Makoto Nakajima 《Tetrahedron letters》2013
An application of a hypervalent silicon complex, generated from a chiral phosphine oxide catalyst and silicon tetrachloride, to the enantioselective organocatalytic Morita–Baylis–Hillman reaction is described. A chloride anion liberated from the hypervalent silicon complex smoothly generated a γ-chloro silyl enol ether that subsequently reacted with an aldehyde to afford the Baylis–Hillman adducts in good yields and with good enantioselectivities. 相似文献
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《Tetrahedron: Asymmetry》1998,9(16):2857-2864
The key intermediate 18 for the synthesis of (−)-ovalicin was synthesized using (−)-quinic acid as the chiral source, through a series of stereocontrolled and efficient chemical reactions, thus establishing a new, formal synthesis of the natural target. The featuring spirocyclic epoxide function has been installed by internal Williamson ether synthesis using the functionalities originally present at C-1 of (−)-quinic acid after the appropriate adjustments required to introduce the necessary functionality at C-2. 相似文献