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131.
Amii H Ichihara Y Nakagawa T Kobayashi T Uneyama K 《Chemical communications (Cambridge, England)》2003,(23):2902-2903
N-Allylic difluoroenamines exhibited unusual behaviors under thermal conditions; N-allyl difluoroenamines in refluxing xylene afforded not only aza-Claisen rearrangement products, but also 2-azabicyclo[2.1.1]hexanes, whose formation could be explained via intramolecular [2+2]-cycloaddition, whilst N-prenyl difluoroenamine underwent an ene reaction to give the pyrrolidine as a sole product. 相似文献
132.
[reaction: see text] A Mg(0)/Me(3)SiCl system was found to be effective for the preparation of a novel fluorinated dianion equivalent. A one-pot reaction sequence involving reductive C-F and C-Cl bond cleavage reactions of trifluoroacetimidoyl chlorides afforded bis-silylated difluoroenamines. Subsequent carbon-carbon bond-forming reactions of the bis(silyl)enamines with two kinds of electrophiles gave a variety of difluorinated imines. 相似文献
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138.
Koji Nuida Satoshi Fujitsu Manabu Hagiwara Takashi Kitagawa Hajime Watanabe Kazuto Ogawa Hideki Imai 《Designs, Codes and Cryptography》2009,52(3):339-362
It has been proven that the code lengths of Tardos’s collusion-secure fingerprinting codes are of theoretically minimal order
with respect to the number of adversarial users (pirates). However, the code lengths can be further reduced as some preceding
studies have revealed. In this article we improve a recent discrete variant of Tardos’s codes, and give a security proof of
our codes under an assumption weaker than the original Marking Assumption. Our analysis shows that our codes have significantly
shorter lengths than Tardos’s codes. For example, when c = 8, our code length is about 4.94% of Tardos’s code in a practical setting and about 4.62% in a certain limit case. Our
code lengths for large c are asymptotically about 5.35% of Tardos’s codes.
A part of this work was presented at 17th Applied Algebra, Algebraic Algorithms, and Error Correcting Codes (AAECC-17), Bangalore,
India, December 16–20, 2007. 相似文献
139.
Ayumi Ishii Shinobu Kishi Hideki Ohtsu Toshifumi Iimori Takakazu Nakabayashi Nobuhiro Ohta Naoto Tamai Milan Melnik Miki Hasegawa Yuzo Shigesato 《Chemphyschem》2007,8(9):1345-1351
The electronic and structural behaviour of a Pr(III) complex with 4,7-diphenyl-1,10-phenanthroline, [Pr(bathophen)(2)(NO(3))(3)], is investigated with respect to the effect of configuration changes on the Pr(III) centre. [Pr(bathophen)(2)(NO(3))(3)] luminesces from the excited states of the ligand and the metal ion. The fluorescence, ff-emission ((1)D(2)-->(3)H(4)), and phosphorescence bands appear at 394, 608.2 and 482 nm, respectively, in the solid state. In acetonitrile, the complex also shows multiple emissions. From the time-resolved emission and the lifetime measurements, the excitation energy-transfer in [Pr(bathophen)(2)(NO(3))(3)] is clarified, that is, the upper excited triplet level of the ligand acts as an energy donor, while the (1)D(2) levels of Pr(III) is the acceptor. Additionally, the emission phenomena of the complex can be modified by molecular distortion, particularly by rotation of the phenyl groups in the ligand. 相似文献
140.
Reaction of 2-propargylphenylcarbamates with diphenyliodonium salts via Meyer-Schuster rearrangement
Hideki Minami Noriko Okamoto Takuya Sueda Takatsugu Sakaguchi Minoru Ishikura Reiko Yanada 《Tetrahedron letters》2017,58(45):4277-4280
The syntheses of 2,3-dihydro-4-quinolones from 2-propargylphenylcarbamates by one-pot tandem process that involves Meyer-Schuster rearrangement or arylative Meyer-Schuster rearrangement/Michael addition of carbamate nitrogen to the resulting vinyl ketones have been developed. Phenylcarbamates tethering tertiary propargyl alcohols underwent arylative Meyer-Schuster rearrangement/Friedel-Crafts alkylation to produce 2,3-dihydroindenones. 相似文献