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Toshihide Maki Dr. Shinya Iikawa Gen Mogami Hitomi Harasawa Yoshihiro Matsumura Prof. Dr. Osamu Onomura Prof. Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(21):5364-5370
Get selective! A selective oxidation of 1,2‐diols to α‐hydroxyketones catalyzed by organotin compounds has been developed (see scheme). Invaluable chemo‐ and stereoselectivity were found in the reaction. The catalytic system has been achieved by electrochemical and chemical oxidation.
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Fengtao Fan Keju Sun Zhaochi Feng Dr. Haian Xia Bo Han Yuxiang Lian Pinliang Ying Dr. Can Li Prof. Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(13):3268-3276
The nucleation process of iron‐exchanged zeolite Fe‐ZSM‐5, from the assembly of distorted tetrahedrally coordinated iron species and silicate rings in the precursor to the final Fe‐ZSM‐5 crystals, as well as variations in the coordination environment of iron, were studied by UV resonance Raman spectroscopy and complementary techniques.
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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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Renata Marcia de Figueiredo Dr. 《Angewandte Chemie (International ed. in English)》2009,48(7):1190-1193
Diaminations are a girl's best friend : New reactions in the field of transition‐metal‐catalyzed diamination of olefins provide a powerful tool for the elaboration of more complex molecules bearing the 1,2‐diamine moiety. An overview of these methods, including asymmetric versions, is given.
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Yutaka Maeda Prof. Akiko Sagara Masahiro Hashimoto Yuya Hirashima Katsuya Sode Tadashi Hasegawa Prof. Makoto Kanda Midori O. Ishitsuka Dr. Takahiro Tsuchiya Dr. Takeshi Akasaka Prof. Toshiya Okazaki Prof. Hiromichi Kataura Prof. Jing Lu Prof. Shigeru Nagase Prof. Seiji Takeuchi 《Chemphyschem》2009,10(6):926-930
Reversible and non‐bonding interaction between SWNTs and ODCB is observed from the analyses of visible near‐infrared absorption data and Raman spectroscopies (see spectra). The solvent effect on SWNTs effectively controls the electronic structure of SWNTs under homogeneous conditions.
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Jung Hee Yoon Dae Won Ryu Hyoung Chan Kim Dr. Sung Won Yoon Byoung Jin Suh Prof. Chang Seop Hong Prof. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(15):3661-3665
Two‐step magnetic transitions : An azide‐bridged 1D MnIII coordination polymer with a unique single end‐on mode was prepared; it displayed atypical antiferromagnetic couplings and field‐induced two‐step magnetic transitions (see figure). The spin‐canted phenomenon in the antiferromagnetic chain complex plays a pivotal role in establishing the slow magnetic relaxation.
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Philipp Selig Dr. Eberhardt Herdtweck Dr. Thorsten Bach Prof. Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(14):3509-3525
The stereogenic centers at C3 and C12 of meloscine ( 3 ) can be established in the photochemical key step 1 → 2 . 1,2‐retro‐Benzilic acid rearrangement to a five‐membered ring, reductive amination, Claisen rearrangement, and ring‐closing metathesis are further key steps in the transformation of cyclobutane 2 into the target molecule 3 (14 steps, 9 % overall yield). Enantioselective access to (+)‐meloscine was possible when the [2+2]‐photocycloaddition was conducted in the presence of a chiral template.
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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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Tony K. M. Shing Prof. Dr. Wai F. Wong Dr. Taketo Ikeno Prof. Dr. Tohru Yamada Prof. Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(11):2693-2707
From sugar to cycloadduct : The effect of the trans‐acetonide blocking group and the stereochemistry of the substituents on the regio‐ and stereoselectivity in the intramolecular nitrone–alkene cycloaddition (INAC) reaction of hept‐6‐enoses (see scheme) is reported and studied by using theoretical analysis.
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Yi Liu Dr. Li‐Ming Wu Prof. Dr. Long‐Hua Li Shao‐Wu Du Prof. Dr. John D. Corbett Prof. Dr. Ling Chen Prof. Dr. 《Angewandte Chemie (International ed. in English)》2009,48(29):5305-5308
In phase : The title compounds lie in a new region of phase space for such a structure, and have stoichiometries in accord with a classical Zintl phase formulation. The small semiconductor gaps indicated by DFT calculations are also supported by their diamagnetic susceptibilities.
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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.