Recognition of ring pairs in the data analysis of Cherenkov detectors

We present a new algorithm for the identification of ring pairs in Cherenkov detectors. The approach combines linear regression methods for the construction of an appropriate reference quantity, methods from statistics for the evaluation of hypotheses and Monte Carlo simulation runs for the tuning of threshold levels.     

微型圆光栅刻划偏心量的控制

对微型圆光栅刻划偏心误差问题进行了讨论。提出了微型圆光栅刻划时偏心调试误差的公差范围。     

含嘧啶环的双冠醚(Ⅳ)

前文已报道由啶环桥联两个苯并冠醚的双冠醚的合成与性质。由于嘧啶环的刚性较大,能把两个冠醚单元固定在有效地协同作用位置,因此以它们作中性载体的离子选择性电极具有较好的选择性。为了进一步研究这类双冠醚的性质,我们合成了四种嘧啶环桥联两个脂肪族冠醚的双冠醚,并经元素分析、IR、′HNMR鉴定。     

Michael and ring expansion reactions of 6-carboethoxy-3,5-diaryl-2-cyclohexen-1-ones

When -keto-ester1 a was reacted with dimethyl acetylenedicarboxylate ring expansion occurred to give substituted cyclooctadienones.Michael reactions of the title compounds1 with unsaturated ketones gave adducts, some of which underwent further cyclization reactions. A new route to -tetralone ring system10 via cyclization of the intermediateMichael adduct9 is described.

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Michael- und Ringerweiterungsreaktionen von 6-Carboethoxy-3,5-diaryl-2-cyclohexen-1-onen

Zusammenfassung Bei der Reaktion von -Keto-ester1 a mit Dimethyl-acetylendicarboxylat wurden unter Ringerweiterung substituierte Cyclooctadienone erhalten. DieMichael-Reaktion der Titelverbindung1 mit ungesättigten Ketonen ergab Addukte, von denen einige weitere Cyclisierungsreaktionen eingingen. Es wird ein neuer Weg zum -Tetralonsystem10 über die Cyclisierung des intermediärenMichael-Addukts9 beschrieben.

     

Microwave-assisted conversion of N-substituted oxazolidin-2,4-diones into α-hydroxyamides

N-Substituted oxazolidin-2,4-diones have been synthesized in a novel one-pot reaction by reacting cyanohydrins stepwise with 1,1′-carbonyldiimidazole and primary amines followed by acidic hydrolysis of the intermediate 4-imino-oxazolidin-2-ones. Their microwave-assisted conversion into α-hydroxyamides was accomplished by treatment with catalytic amounts of sodium methoxide in methanol.     

新型2-氧代-1,2,4-三唑并[3,2-d][1,5]苯并氧氮杂类稠杂环的合成

将取代色满酮(1)与芳肼反应生成的腙与HNCO发生[3+2]环加成反应,加成产物(2)经氧化得到偕偶氮异氰酸酯(3).化合物3在HBF4的催化下发生环化-重排反应,得到新颖的三环系2-氧代-1,2,4-三唑并[3,2-d][1,5]苯并氧氮杂化合物5a～5g.     

A non-catalytic approach to the synthesis of 5,6-dihydrobenzo[h]quinolines

A concise synthesis of highly functionalized 5,6-dihydrobenzo[h]quinoline-3-carbonitriles is delineated through base induced ring transformation of 4-sec-amino-2-oxo-5,6-dihydro-2H-benzo[h]chromene-3-carbonitriles with S-methylisothiourea sulfate and 1-carboxamidinepyrazole hydrochloride, separately, in DMF. Under analogous reaction conditions the ring transformation of 4-sec-amino-2-oxo-5,6-dihydro-2H-benzo[h]chromene-3-carbonitriles by formamidine acetate provided 4-sec-amino-benzo[h]quinoline-3-carbonitriles in moderate yields, while with benzamidine hydrochloride, the reaction followed the same mechanism to yield 2-phenyl-4-sec-amino-5,6-dihydrobenzo[h]quinoline-3-carbonitriles.     

An unusual synthesis of tetrahydrobenzo[f]isoquinolines

A facile and short synthesis of 2-oxo-4-sec-amino-2,3,5,6-tetrahydrobenzo[f]isoquinoline-1-carbonitriles has been delineated through base catalyzed ring transformation of 5,6-dihydro-2-oxo-4-sec-amino-2H-benzo[h]chromene-3-carbonitrile by cyanoacetamide in excellent yields.     

A convenient synthesis of 2-aryl substituted benzo[f] [1,2,4]triazolo[1,5-a]azepine derivatives

A convenient synthetic pathway to 2-aryl-5,6-dihydro-4H-benzo[f][1,2,4]triazolo[1,5-α]azepine derivatives 7 was developed. The synthesis was based on the cycloaddition of the 1,2,3,4-tetrahydronaphthalene a-acetoxy azo compounds 3 with Ar-CN in the presence of AlCl3 and the consecutive ring enlargement.     

Palladium-catalyzed synthesis of poly(bromoalkoxy- and bromoalkanoyloxymethylsiloxane)s from poly(hydromethylsiloxane)s

Palladium-catalyzed synthesis of poly(bromoalkoxymethyl- and bromoalkanoyloxymethylsiloxane)s from poly(hydromethylsiloxane)s was studied. Treatment of poly(hydromethylsiloxane)s with mixtures of allyl bromide and cyclic ethers in the presence of a catalytic amount of PdCl₂ gave the corresponding poly[(bromoalkoxy)methylsiloxane]s in good yield. A similar reaction with γ-butyrolactone produced poly[(bromobutanoyloxy)methylsiloxane], although the polymer was highly moisture-sensitive and could not be separated from the reaction mixture. Transformation of the bromoalkoxy unit in the resulting siloxane polymer into an aminoalkoxy group was also examined.