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Self-assembled monolayers of organosulfur compounds on gold incorporating terminal conjugated arenes, redox active probes, and oligonucleotides /Reese, Raymond Scott, January 1998 (has links)
Thesis (Ph. D.)--University of Texas at Austin, 1998. / Vita. Includes bibliographical references (leaves 181-192). Available also in a digital version from Dissertation Abstracts.
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Infra-red spectra of olefines and organic sulphur compounds, with some applications to the structure and vulcanisation of rubber.Sheppard, Norman. January 1947 (has links)
Thesis--St. Catharine's College, Cambridge. / Typescript (carbon) with ms. corrections. Without thesis statement. Appendices 1-3 by N. Sheppard and G.B.B.M. Sutherland. Bibliography: leaves 209-216.
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Structural studies of several organometallic complexes containing sulfur of phorusColeman, Judith Margaret, January 1966 (has links)
Thesis (Ph. D.)--University of Wisconsin, 1966. / Typescript. Vita. eContent provider-neutral record in process. Description based on print version record. Includes bibliography.
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Studies on Catalytic Transformations of Organosulfur Compounds via C-S Bond Cleavage / 有機硫黄化合物の炭素-硫黄結合切断を経る触媒的変換反応に関する研究Otsuka, Shinya 25 March 2019 (has links)
京都大学 / 0048 / 新制・課程博士 / 博士(理学) / 甲第21587号 / 理博第4494号 / 新制||理||1645(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 依光 英樹, 教授 大須賀 篤弘, 教授 丸岡 啓二 / 学位規則第4条第1項該当 / Doctor of Science / Kyoto University / DGAM
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Studies on Nickel-Catalyzed Reactions via Alkyne Insertion into Carbon-Sulfur Bonds / ニッケル触媒による炭素-硫黄結合へのアルキン挿入を伴う反応に関する研究Inami, Tasuku 23 March 2015 (has links)
京都大学 / 0048 / 新制・課程博士 / 博士(工学) / 甲第18950号 / 工博第3992号 / 新制||工||1615(附属図書館) / 31901 / 京都大学大学院工学研究科材料化学専攻 / (主査)教授 松原 誠二郎, 教授 辻 康之, 教授 中尾 佳亮 / 学位規則第4条第1項該当 / Doctor of Philosophy (Engineering) / Kyoto University / DGAM
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Organopolychalcogenides, new bond energy results and synthesis via the first selenium transfer reagentRyan, M. Dominic (Michael Dominic) January 1988 (has links)
No description available.
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1, 3, 2- dioxaphospholene sulfenyl chloride condensation.Mathiaparanam, Ponnampalam. January 1970 (has links)
No description available.
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Development of Efficient Methods for the Synthesis of Organosulfur (IV) Compounds / 4価有機硫黄化合物の効率的合成法の開発Tsuzuki, Saori 25 March 2024 (has links)
京都大学 / 新制・課程博士 / 博士(理学) / 甲第25135号 / 理博第5042号 / 京都大学大学院理学研究科化学専攻 / (主査)教授 依光 英樹, 教授 畠山 琢次, 教授 松永 茂樹 / 学位規則第4条第1項該当 / Doctor of Science / Kyoto University / DGAM
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Synthesis, structural characterization and applications of homoleptic organosulfur and organoselenium metal polymersLow, Kam-hung., 魯錦鴻. January 2009 (has links)
published_or_final_version / Chemistry / Doctoral / Doctor of Philosophy
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Síntese e funcionalização de compostos organoenxofre: sulfóxidos, sulfetos e N-sulfinil iminas / Synthesis and functionalization of organosulfur compounds: sulfoxides, sulfides and N-sulfinyl iminesSouza, Frederico Bernardes de 22 September 2017 (has links)
Neste trabalho promovemos a síntese de sulfóxidos vinílicos ?-substituídos através da reação de acoplamento cruzado de Suzuki-Miyaura. Também foi feita a síntese de sulfóxidos enínicos inéditos, pela adição do nucleófilo no carbono β-sulfóxido. Esses compostos eram passíveis de serem submetidos a reação de rearranjo de Pummerer aditivo e assim gerarem uma pequena biblioteca de compostos α-tioaldeídos. Um desses aldeídos sintetizados foi empregado na reação de formação de uma imina propargílica, com consequente reação de CuAAC formando iminas triazólicas. Outras iminas arílicas foram sintetizadas, passando por uma etapa de redução, com intuito de se obter a amina livre, para que fosse feita a reação de ciclização com auxílio de um agente eletrofílico. Outra classe de composto organoenxofre foi sintetizada, as N-sulfinil imina, que após a reação de acoplamento cruzado de Sonogashira, com consequente remoção de um grupo protetor e a formação do anel heterocíclico, foram obtidos compostos triazólicos N-sulfinil imínicos. / In this work we promote the synthesis of α-substituted vinylic sulfoxides through the Suzuki-Miyaura cross coupling reaction. Also the synthesis of unpublished enynic sulfoxides was made, by the addition of the nucleophile in the β-sulfoxide carbon. These compounds were susceptible to additive Pummerer rearragement reaction and thus generated a small library of compounds. One of these aldehydes synthesized was used in the formation reaction of a propargyl imine, with consequent CuAAC reaction, forming triazol imines. Other aryl imines were synthesized, undergoing a reduction step, in order to obtain the free amine, so that the cyclization reaction was carried out with the aid of an electrophilic agent. Another class of organosulfur compound was synthesized, the N-sulfinyl imine, which after the Sonogashira cross-coupling reaction, with consequent removal of a protecting group and formation of the heterocyclic ring, N-sulfinyl imine triazolic compounds were obtained.
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