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81.
Vitale M Lecourt T Sheldon CG Aggarwal VK 《Journal of the American Chemical Society》2006,128(8):2524-2525
The reaction of lithiated trimethylsilyldiazomethane (LTMSD) with aldehydes and subsequent quenching with TMSCl furnished relatively stable alpha-silylated diazocompounds. Upon treatment of the alpha-silylated diazocompounds with Rh2(OAc)4 in refluxing toluene, alpha-silyl silyl enol ethers were formed from unbranched and branched aliphatic aldehydes through predominantly 1,2-migration of the C-H bond. In contrast, treatment of the alpha-silylated diazocompounds with Rh2(tfa)4 at room temperature gave alpha-silyl silyl enol ethers through exclusive and unusual 1,2-migration of the C-C bond. The origin of the selectivity observed from the two catalysts is discussed in relation to early and late transition states. 相似文献
82.
In this paper, we present and apply a computer-assisted method to study steady states of a triangular cross-diffusion system. Our approach consist in an a posteriori validation procedure, that is based on using a fixed point argument around a numerically computed solution, in the spirit of the Newton–Kantorovich theorem. It allows to prove the existence of various non homogeneous steady states for different parameter values. In some situations, we obtain as many as 13 coexisting steady states. We also apply the a posteriori validation procedure to study the linear stability of the obtained steady states, proving that many of them are in fact unstable. 相似文献
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85.
A stereocontrolled total synthesis of (+)-longicin, a representative of the class of mono-THF-acetogenins, is described. The strategy involves the utilization of d- and l-glutamic acids as chirons that correspond to two five-carbon segments harboring stereogenic centers at C4 and at C17 of the C(32) polyketide-derived natural product. The use of Grubbs' RCM reaction as a novel "chain elongation" strategy for the synthesis of acetogenin-type structures and a new protocol for butenolide incorporation are also described. [structure: see text] 相似文献
86.
Maxime D. Crozet 《Tetrahedron letters》2006,47(39):7061-7065
A new simple, rapid and high yielding synthesis of various 6-aryl-2-arylsulfonylmethyl-3-nitroimidazo[1,2-a]pyridines by Suzuki cross-coupling reaction is described using microwave irradiation in aqueous medium without organic co-solvent in the presence of tetrabutylammonium bromide. 相似文献
87.
Wise CA Paris M Morar B Wang W Kalaydjieva L Bittles AH 《Rapid communications in mass spectrometry : RCM》2003,17(11):1195-1202
Analysis of single nucleotide polymorphisms (SNPs) has become an increasingly important area of research, with numerous applications in medical genetics, population genetics, forensic science, and agricultural biotechnology. Large-scale SNP analyses require the development of methodologies that are economical, flexible, accurate and capable of automation. Primer extension in conjunction with matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOFMS) is currently emerging as a potential method for high-throughput SNP genotyping. We have evaluated a number of published primer extension methods and refined a simple and robust protocol to analyze human autosomal disease-causing mutations and population genetic markers on the Y-chromosome. Twelve different variant sites were examined, and homozygotes, heterozygotes and hemizygotes were accurately typed. A 100% concordance was observed between SNP genotypes obtained using the MALDI-TOFMS technique and alternative genotyping methods, such as restriction fragment length polymorphism (RFLP) assays and denaturing high-performance liquid chromatography (DHPLC). Since multiple polymorphisms can be detected in single reactions, the method provides a cost-effective approach for SNP analysis. The protocol is also extremely flexible (able to accommodate new markers) and can be adapted to a number of platforms without the use of commercial kits. 相似文献
88.
Maxime Robin Stphane Mialhe Valrie Pique Robert Faure Jean‐Pierre Galy 《Journal of heterocyclic chemistry》2002,39(2):295-298
Novel 7,8,9,10‐tetrahydrothiazolo[5,4‐a]acridine and 1,2,3,4‐tetrahydro‐12H‐benzothiazolo[2,3‐b]‐quinazolin‐12‐one derivatives were synthesized in one step from the corresponding benzothiazoles. These two new tetracyclic skeletons were unambiguously characterized and are presently in pharmacological tests. 相似文献
89.
Valrie Sciannamea Maxime Bernard Jean‐Marie Catala Robert Jrme Christophe Detrembleur 《Journal of polymer science. Part A, Polymer chemistry》2006,44(21):6299-6311
The C‐phenyl‐N‐tert‐butylnitrone/azobisisobutyronitrile pair is able to impart control to the radical polymerization of n‐butyl acrylate as long as a two‐step process is implemented, that is, the prereaction of the nitrone and the initiator in toluene at 85 °C for 4 h followed by the addition and polymerization of n‐butyl acrylate at 110 °C. The structure of the in situ formed nitroxide has been established from kinetic and electron spin resonance data. The key parameters (the dissociation rate constant, combination rate constant, and equilibrium constant) that govern the process have been evaluated. The equilibrium constant between the dormant and active species is close to 1.6 × 10?12 mol L?1 at 110 °C. The dissociation rate constant and the activation energy for the C? ON bond homolysis are 1.9 × 10?3 s?1 and 122 ± 15 kJ mol?1, respectively. The rate constant of recombination between the propagating radical and the nitroxide is as high as 1.2 × 109 L mol?1 s?1. Finally, well‐defined poly(n‐butyl acrylate)‐b‐polystyrene block copolymers have been successfully prepared. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 6299–6311, 2006 相似文献
90.