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A study of the reaction of N-chloroamines with electron-rich aromatic compoundsTaylor, J. M. January 1987 (has links)
No description available.
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Substitution of polyhalogenoaromatic compounds by sterically hindered nucleophilesCheong, C. L. January 1986 (has links)
No description available.
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Radicals and reactive ringsSherburn, Michael S. January 1990 (has links)
No description available.
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Kinetics and mechanism of thalliation of aromatic petrochemicals in trifluoroacetic acidAl-Azzawi, S. F. A. January 1984 (has links)
No description available.
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Some sigmatropic rearrangements of polyfluoroaromatic and heteroaromatic compoundsFerguson, John Alasdair Kerr Jamie January 1986 (has links)
This Thesis describes some [3,3] and [2,3] -sigmatropic rearrangements that can occur in a variety of polyfluoroaromatic and -heteroaromatic compounds. The presence of fluorine on the aromatic moiety precludes the normal rearomatization process. The work is conveniently divided into two parts. Part A concerns the preparation and thermal (Claisen) rearrangement of derivatives of allyl 5-fluoropyrimidin-4-yl ether. These rearrange upon thermolysis to give isomers in which the terminus for the migration of the allyl group is N-3, provided that there is no preceding reaction which localises a double- bond between C-4 and C-5 - in which case C-5 is the migration terminus. Hydrolysis of some of the N-allyl derivatives results in the formation of some new derivatives of 5-fluorouracil. Part B describes the reactions that occur when polyfluor - inated monocyclic, polycyclic and heterocyclic ring systems are treated with dimethylsulphoxide activated by dicyclohexycarbodi-imide or by trifluoroacetic anhydride. Fluorinated phenolic type compounds give products which are the result of a [2,3] sigmatropic rearrangement of the derived sulphoniumylide. Fluorinated anilines and thiophenols behave differently. Dearomatization occurs under very mild conditions. A number of reactions of the fluorinated cyclohexa-2,4-dienone products are described. The preparation and attempted rearrangement of 2,3,4,5,6- pentafluorobenzylmethylsulphoxide is also discussed.
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Synthetic Studies on Heteraazulenes Containing a Heavy Group 14 Element as a Skeletal Element / 高周期14族元素を骨格構成元素として含むヘテラアズレン類の合成研究Oshiro, Taku 23 March 2022 (has links)
京都大学 / 新制・課程博士 / 博士(理学) / 甲第23718号 / 理博第4808号 / 新制||理||1688(附属図書館) / 京都大学大学院理学研究科化学専攻 / (主査)教授 時任 宣博, 教授 依光 英樹, 教授 若宮 淳志 / 学位規則第4条第1項該当 / Doctor of Science / Kyoto University / DGAM
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Impacts of Exposure to Polycyclic Aromatic Compounds (PACs) and Their Alkylated Congeners in North American River Otter (Lontra canadensis)Thomas, Philippe 28 August 2020 (has links)
Polycyclic aromatic compounds (PACs) are a group of chemicals encompassing thousands of different aromatic, alkyl aromatic and heterocyclic hydrocarbons (i.e.- containing N, S, or O- atoms); 16 of which have been designated as priority pollutants due to their toxicity and prevalence. Several studies have highlighted increases in the concentrations of C1-C4 alkylated PACs and heterocyclic aromatic hydrocarbons such as dibenzothiophenes in the atmosphere, water, soil and sediments, plants, wildlife and fish in the Athabasca Oil Sands Region (AOSR). Although there has been considerable research attention related to the toxic, carcinogenic and mutagenic properties of PACs, there is an increasing awareness that these chemicals may also have profound endocrine disrupting properties in wildlife. North American river otter (Lontra canadensis) are good indicators of ecosystem health due to their ecology and sensitivity to environmental pollutants. In this thesis, we first demonstrated the utility of adopting paleotoxicological frameworks in defining environmental baseline levels of PACs and likely biological effects from exposure to these complex environmental mixtures. These methods allowed us to reconstruct historical PAC deposition patterns to impacted areas while simultaneously determining likely biological effects such as endocrine disruption. Next, we showed how PACs exhibited trophic dilution in a Boreal food chain dominated by river otters. Snails, prey and predator fish, as well as river otters were collected from four main study areas in the AOSR in northeastern Alberta, Canada. Bioaccumulation factors such as biota-sediment accumulation factors (BSAF) and trophic magnification factors (TMF) were used to evaluate the partitioning behavior of PACs in the environment and subsequent risks to biota. Our results revealed localized enrichment of certain PACs and subsequent metabolism in higher order vertebrates. Finally, we successfully combined ecotoxicological and physiological analyses paired with population genetic estimates to investigate endocrine disruption and population-level responses to exposure to PACs. River otters are known for their habitual use of latrine sites. Latrine sites represent a unique opportunity for biomonitoring programs to study river otters using indirect sampling methods. In this thesis, PACs were characterized and evaluated in sediment, lower and higher trophic biota with demonstrated impacts on endocrine processes and river otter population health. Effects-based assessments such as the ones presented in this thesis are more powerful for environmental monitoring programs than stressor-based assessment methods (such as describing presence/absence or levels of contaminants) as they provide greater biological context to monitoring data. In turn, these are helpful in selecting triggers for environmental effects monitoring or adaptive management programs.
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Organocatalytic Diboration and Silaboration Based on Pyridine-Mediated Activation of Boron-Containing σ-Bond / ピリジン化合物による含ホウ素σ結合活性化に基づく有機分子触媒ジホウ素化およびシリルホウ素化Morimasa, Yohei 26 July 2021 (has links)
京都大学 / 新制・課程博士 / 博士(工学) / 甲第23432号 / 工博第4887号 / 新制||工||1764(附属図書館) / 京都大学大学院工学研究科合成・生物化学専攻 / (主査)教授 杉野目 道紀, 教授 村上 正浩, 教授 大江 浩一 / 学位規則第4条第1項該当 / Doctor of Philosophy (Engineering) / Kyoto University / DFAM
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Development of Novel Conjugated Compounds Based on Characteristics of Gallium Element / ガリウム原子の特性を活用した共役系化合物群の創出Takuya, Matsumoto 23 March 2015 (has links)
京都大学 / 0048 / 新制・課程博士 / 博士(工学) / 甲第19005号 / 工博第4047号 / 新制||工||1623(附属図書館) / 31956 / 京都大学大学院工学研究科高分子化学専攻 / (主査)教授 中條 善樹, 教授 澤本 光男, 教授 田中 一義 / 学位規則第4条第1項該当 / Doctor of Philosophy (Engineering) / Kyoto University / DGAM
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Syntheses of Polycyclic Aromatic Compounds with Heteroatom Junctions via Tandem Hetero-Friedel-Crafts Reactions / タンデムヘテロフリーデルクラフツ反応を活用したヘテロ元素縮環部位を有する多環芳香族化合物群の合成Hashimoto, Sigma 25 March 2013 (has links)
Kyoto University (京都大学) / 0048 / 新制・課程博士 / 博士(工学) / 甲第17584号 / 工博第3743号 / 新制||工||1570(附属図書館) / 30350 / 京都大学大学院工学研究科物質エネルギー化学専攻 / (主査)教授 中村 正治, 教授 大江 浩一, 教授 村田 靖次郎 / 学位規則第4条第1項該当
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