共查询到20条相似文献,搜索用时 562 毫秒
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Romas Kudirka Sean K. J. Devine Christopher S. Adams David L. Van Vranken Prof. 《Angewandte Chemie (International ed. in English)》2009,48(20):3677-3680
As easy as 1, 2, 3 : A palladium‐catalyzed three‐component coupling generates α,β‐unsaturated γ‐amino acids in a single step (see scheme). The reaction is believed to involve migration of a vinyl substituent to a highly electrophilic palladium carbene. Unlike previous synthetic approaches, this synthesis provides access to γ‐amino acids with non‐natural side chains.
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Soluble InP and GaP Nanowires: Self‐Seeded,Solution–Liquid–Solid Synthesis and Electrical Properties
Zhaoping Liu Kai Sun Dr. Wen‐Bin Jian Prof. Dr. Dan Xu Yen‐Fu Lin Jiye Fang Prof. Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(18):4546-4552
A facile, self‐seeded , solution–liquid–solid growth of soluble InP and GaP nanowires with a very low amount of native point defects with respect to the carrier concentrations have been synthesized (see scheme) and characterized. They are potentially promising building blocks in optoelectronic applications.
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Jinping Chen Dr. Masatoshi Mizumura Hiroshi Shinokubo Prof. Dr. Atsuhiro Osuka Prof. Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(24):5942-5949
Two series of BODIPY dyes with substituents either in the α positions or in the β positions and different conjugation lengths were synthesized by means of iridium‐catalyzed borylation and rhodium‐catalyzed Heck‐type addition (see scheme). The α‐ and β‐substituted series show completely different photophysical properties. BODIPY=boron dipyrrin.
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Carla T. Cioffi Dr. Amit Palkar Dr. Frederic Melin Dr. Amar Kumbhar Luis Echegoyen Prof. Dr. Manuel Melle‐Franco Francesco Zerbetto Prof. Dr. G. M. Aminur Rahman Dr. Christian Ehli Vito Sgobba Dr. Dirk M. Guldi Prof. Dr. Maurizio Prato Prof. Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(17):4419-4427
Don't cry! The attachment of ferrocene moieties on the surface of carbon nano‐onions influences the electrochemical properties of these moieties and the photophysical properties of the carbon nano‐onions (see figure). Quantum chemical calculations confirm that the spectral properties of carbon nano‐onions depend on their size and the degree of functionalisation.
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Hai‐Hua Lu Hui Liu Dr. Wei Wu Xu‐Fan Wang Liang‐Qiu Lu Wen‐Jing Xiao Prof. Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(12):2742-2746
Economical approach : The first organocatalytic asymmetric intramolecular hydroarylation of phenol‐ and aniline‐derived enals offers one of the most straightforward and atom‐economic approaches to enantioriched chromans and tetrahydroquinolines (up to 96 % ee; see scheme).
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Qingwei Meng Dr. Xiao‐Hua Sun Dr. Zhengyu Lu Ping‐Fang Xia Zehua Shi Dongzhong Chen Prof. Dr. Man Shing Wong Prof. Dr. Salem Wakim Dr. Jianping Lu Dr. Jean‐Marc Baribeau Dr. Ye Tao Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(14):3474-3487
Supramolecular chirality and liquid crystalline OFET : Achiral end‐capped oligothiophenes can be tuned to exhibit supramolecular chirality with unique striped textures showing distinct circular dichroism signals as well as a highly ordered SmE phase that leads to high hole carrier mobility.
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A convenient route with high stereo control to γ‐acetoxy dienoates is provided by the reaction of methyl propiolate with aldehydes in the presence of ZnEt2 and N‐methylimidazole at room temperature, followed by the catalytic conversion of the resulting γ‐hydroxy‐α,β‐acetylenic esters with p‐N,N‐dimethylaminopyridine (DMAP) in acetic anhydride (see scheme).
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Weiwei Liu Yueqiang Zhao Shujiang Tu Ting He Hongwen Hu 《Journal of heterocyclic chemistry》2008,45(5):1311-1314
3‐Thioformylindolizines undergo novel reductive coupling reaction in the presence of tributylphosphine to give E‐1,2‐bis(3‐indolizinyl)ethylenes in high yield. These reactions proceed via (3‐indolizinyl)methylene carbene intermediate and provide a new, stereoselective synthesis of the bis(3‐indolizinyl)ethylene derivatives highly. 相似文献
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Sung Ho Kim Dr. Fredrik Nederberg Dr. Robert Jakobs Jeremy P. K. Tan Dr. Kazuki Fukushima Dr. Alshakim Nelson Dr. E. W. Meijer Prof. Dr. Yi Yan Yang Prof. Dr. James L. Hedrick Dr. 《Angewandte Chemie (International ed. in English)》2009,48(25):4508-4512
Once around the block : Incorporation of a rigid hydrogen‐bonding benzamide unit, placed at the interface between two polymer blocks, in poly(ethylene glycol) (PEG)–(thio)urea–poly(L ‐lactide) (PLLA) block copolymers transforms the morphology of the block copolymers, from spherical micelles, as formed by PEG‐PLLA diblock copolymers, into nanotubes in solution.
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Lei Gong Dr. Zhening Chen Yumei Lin Xumin He Prof. Dr. Ting Bin Wen Prof. Dr. Xin Xu Prof. Dr. Haiping Xia Prof. Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(25):6258-6266
Osmabenzenes can be easily synthesized from two η2‐coordinated olefin osmacycles in the presence of benzonitrile by means of facile hydrogen‐transfer conversions (see graphic). Mechanisms for the formation of osmabenzenes are proposed based on DFT calculations.
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Saravanan Peruncheralathan Dr. Henrik Teller Christoph Schneider Prof. Dr. 《Angewandte Chemie (International ed. in English)》2009,48(26):4849-4852
It's as simple as that : An in situ prepared chiral catalyst from the commercially available compounds Ti(OiPr)4 and (R)‐binol catalyzes the highly enantioselective ring‐opening of meso‐aziridines 1 with anilines 2 and furnishes valuable chiral 1,2‐diamines 3 in high yields and up to 99 % ee.(R)‐binol=(R)‐2,2′‐dihydroxy‐1,1′‐binaphthyl.
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Haifeng Yu Dr. Zhengkun Yu Prof. Dr. 《Angewandte Chemie (International ed. in English)》2009,48(16):2929-2933
Let's make 'meri' : Metal‐free direct alkenylation of indoles was realized by acid‐mediated substitution reactions of α‐oxo ketene dithioacetals with indoles in trifluoroacetic acid/dichloromethane, selectively affording β‐indolyl mono‐ and disubstituted α,β‐unsaturated carbonyl compounds (see scheme). Condensation of the indolyl/ketene monothioacetals and guanidine nitrate efficiently produced meridianin derivatives.