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排序方式: 共有4077条查询结果,搜索用时 31 毫秒
31.
Haoquan Li Dr. Helfried Neumann Prof. Dr. Matthias Beller 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(29):10050-10056
A benign and efficient palladium‐catalyzed aminocarbonylation reaction of allylic alcohols is presented. The generality of this novel process is demonstrated by the synthesis of β,γ‐unsaturated amides including aliphatic, cinnamyl, and terpene derivatives. The choice of ligand is crucial for optimal carbonylation processes: Whereas in most cases the combination of PdCl2 with Xantphos ( L6 ) gave best results, sterically hindered substrates performed better in the presence of simple triphenylphosphine ( L10 ), and primary anilines gave the best results using cataCXium® PCy ( L8 ). The reactivity of the respective catalyst system is significantly enhanced by addition of small amounts of water. Mechanistic studies and control experiments revealed a tandem allylic alcohol amination/C?N bond carbonylation reaction sequence. 相似文献
32.
Dr. Aleksandrs Prokofjevs 《Angewandte Chemie (International ed. in English)》2015,54(45):13401-13405
Thermally induced dehydrogenation of the H‐bridged cation L2B2H5+ (L=Lewis base) is proposed to be the key step in the intramolecular C? H borylation of tertiary amine boranes activated with catalytic amounts of strong “hydridophiles”. Loss of H2 from L2B2H5+ generates the highly reactive cation L2B2H3+, which in its sp2‐sp3 diborane(4) form then undergoes either an intramolecular C? H insertion with B? B bond cleavage, or captures BH3 to produce L2B3H6+. The effect of the counterion stability on the outcome of the reaction is illustrated by formation of LBH2C6F5 complexes through disproportionation of L2B2H5+ HB(C6F5)3?. 相似文献
33.
In this review article recent developments in the asymmetric transfer hydrogenation of imines from 2008 up to today are presented. The main methodology involves either metal‐catalyzed procedures in the presence of a chiral ligand or organocatalyzed technologies using a Hantzsch ester and a chiral BINOL‐derived phosphoric acid. The most important procedures are collected, paying special attention to the application of this methodology in synthetic organic chemistry.
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35.
《Mathematische Nachrichten》2017,290(17-18):2788-2799
A well‐known result of J. Lindenstrauss and A. Pełczyński (1968) gives the existence of a universal non‐weakly compact operator between Banach spaces. We show the existence of universal non‐Rosenthal, non‐limited, and non‐Grothendieck operators. We also prove that there does not exist a universal non‐Dunford–Pettis operator, but there is a universal class of non‐Dunford–Pettis operators. Moreover, we show that, for several classes of polynomials between Banach spaces, including the non‐weakly compact polynomials, there does not exist a universal polynomial. 相似文献
36.
Existing literature regarding the natural hedge potential that arises from combining different longevity-linked liabilities typically does not address the question how changes in the liability mix can be obtained. We consider firms who aim to exploit the benefits of natural hedge potential by redistributing their risks, and characterize the risk redistributions that will arise when the parties bargain for a redistribution of risk that weakly benefits them all. We analyze the effects of heterogeneity in the beliefs regarding the probability distribution of future mortality rates on the properties of these risk redistributions, and provide a numerical illustration for a case where an insurer with a portfolio of term assurance contracts and a pension fund with a portfolio of life annuities redistribute their risks. 相似文献
37.
《Angewandte Chemie (International ed. in English)》2017,56(18):4950-4954
We introduce the synthesis and in‐depth characterization of platinum(II)‐crosslinked single‐chain nanoparticles (PtII‐SCNPs) to demonstrate their application as a recyclable homogeneous catalyst. Specifically, a linear precursor copolymer of styrene and 4‐(diphenylphosphino)styrene was synthesized via nitroxide‐mediated polymerization. The triarylphosphine ligand moieties along the backbone allowed for the intramolecular crosslinking of single chains via the addition of [Pt(1,5‐cyclooctadiene)Cl2] in dilute solution. The successful formation of well‐defined PtII‐SCNPs was evidenced by size exclusion chromatography, dynamic light scattering, nuclear magnetic resonance (1H, 31P{1H}, 195Pt), and diffusion‐ordered spectroscopy. Finally, the activity of the PtII‐SCNPs as homogeneous, yet recyclable catalyst was successfully demonstrated using the example of the amination of allyl alcohol. 相似文献
38.
Robbert van Putten Evgeny A. Uslamin Marcel Garbe Chong Liu Dr. Angela Gonzalez-de-Castro Dr. Martin Lutz Dr. Kathrin Junge Prof. Dr. Emiel J. M. Hensen Prof. Dr. Matthias Beller Dr. Laurent Lefort Prof. Dr. Evgeny A. Pidko 《Angewandte Chemie (International ed. in English)》2017,56(26):7531-7534
Catalytic hydrogenation of carboxylic acid esters is essential for the green production of pharmaceuticals, fragrances, and fine chemicals. Herein, we report the efficient hydrogenation of esters with manganese catalysts based on simple bidentate aminophosphine ligands. Monoligated Mn PN complexes are particularly active for the conversion of esters into the corresponding alcohols at Mn concentrations as low as 0.2 mol % in the presence of sub-stoichiometric amounts of KOtBu base. 相似文献
39.
René Schulz 《偏微分方程通讯》2017,42(5):703-730
We prove that Hörmander’s global wave front set and Nakamura’s homogeneous wave front set of a tempered distribution coincide. In addition, we construct a tempered distribution with a given wave front set, and we develop a pseudodifferential calculus adapted to Nakamura’s homogeneous wave front set. 相似文献
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