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Taichi Ikeda Dr. Masayoshi Higuchi Dr. Dirk G. Kurth Prof. Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(19):4906-4913
Towards polythiophene polyrotaxanes : The β‐substituted terthiophene [2]rotaxanes have been synthesized (see figure). Basic optical and electrochemical properties of the synthesized [2]rotaxanes are also reported.
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Valeria Castelletto Dr. Ian W. Hamley Prof. Rohan A. Hule Dr. Darrin Pochan Prof. 《Angewandte Chemie (International ed. in English)》2009,48(13):2317-2320
An addition to the family : The introduction of β‐amino acid residues into a modified amyloid β peptide fragment resulted in well‐defined helical nanoribbons (see cryo‐TEM image) comprising β strands mainly oriented perpendicular to the ribbon axis. The nanoribbons order into a flow‐aligning nematic phase at higher concentration. The β‐strand nanoribbon structure is an addition to the known set of secondary structures adopted by β‐peptides.
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Toshimichi Ohmura Dr. Yuta Takasaki Hideki Furukawa Michinori Suginome Prof. Dr. 《Angewandte Chemie (International ed. in English)》2009,48(13):2372-2375
Changing places : Intramolecular B(pin)/H exchange took place in the presence of a platinum–phosphane catalyst, giving synthetically useful cis‐β‐methyl‐substituted alkenylboronates stereoselectively (see scheme; B(pin)=4,4,5,5‐tetramethyl‐1,3,2‐dioxaborolan‐2‐yl).
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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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Takuya Hashimoto Dr. Kazuki Sakata Keiji Maruoka Prof. Dr. 《Angewandte Chemie (International ed. in English)》2009,48(27):5014-5017
Going through the phases : The title reaction was found to proceed by an initial base‐mediated isomerization to allenyl esters and subsequent phase transfer catalyzed alkylation at the α position of the ester (see scheme).
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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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Weiying Lin Prof. Lin Yuan Zengmei Cao Yanming Feng Lingliang Long 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(20):5096-5103
Shedding light on thiol detection : A compound (see scheme) was developed as a novel, highly sensitive and selective fluorescent thiol probe, which also features suitable water solubility, functions rapidly under neutral conditions, and has excitation and emission in the visible region. Thus, it may be useful for potential biological applications.
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Ludovic Drouin Dr. E. Cristina Stanca‐Kaposta Dr. Priptal Saundh Antony J. Fairbanks Dr. Sebastian Kemper Timothy D. W. Claridge Dr. John P. Simons Prof. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(16):4057-4069
The effect of carbon is subtle but sweet : The flexible C‐linkage in the newly synthesised C‐glycosyl mimetic, Manα(1,6)‐C‐ManαOPh allows OH? π bonding, both in the gas phase and in aqueous solution. This interaction is absent in the O‐linked disaccharide (see figure).
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Gangavaram V. M. Sharma Dr. Bommagani Shoban Babu Kallaganti V. S. Ramakrishna Pendem Nagendar Dr. Ajit C. Kunwar Dr. Peter Schramm Carsten Baldauf Dr. Hans‐Jörg Hofmann Prof. Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(22):5552-5566
Origami peptides : A novel class of foldamers consisting of α/δ‐hybrid peptides has been investigated theoretically and experimentally by exploiting the rigidity of the side chain of a new δ‐amino acid prepared from D ‐glucose and D ‐xylose with a furanose side chain (see figure).
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