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The acyl-Claisen rearrangement development of a novel metal-catalyzed Claisen rearrangement and enantioselective variants of the acyl-Claisen rearrangement /Yoon, Tehshik Peter. MacMillan, David W. C. January 2002 (has links)
Thesis (Ph. D.)--California Institute of Technology, 2002. PQ #3052855. / Advisor names found in the Acknowledgments pages of the thesis. Title from home page. Viewed 02/11/2010. Includes bibliographical references.
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Chromosomų struktūros persitvarkymų įvairovė Lietuvoje ir genetinė jų reikšmė / Diversity of human chromosome structural rearrangements rearrangement and genetic sequenceČiuladaitė, Živilė 09 July 2011 (has links)
Chromosomų struktūros persitvarkymai gali lemti įvairius žmogaus sveikatos sutrikimus. Netgi chromosominės ligos, pvz., Dauno ar Ternerio sindromai, gali būti nulemtos ne chromosomų skaičiaus, bet chromosomų struktūros persitvarkymų. Chromosomų trūkiai gali vykti bet kurioje chromosomos dalyje, tai lemia įvairius chromosomų struktūros pokyčius, tačiau tik dalis jų yra suderinami su gyvybinėmis funkcijomis ir yra nustatomi postnataliai. Chromosomų struktūros persitvarkymai, priklausomai nuo to, subalansuoti ar nesubalansuoti, lemia įvairias dismorfines anomalijas arba vaisingumo problemas. Jų nustatymas yra svarbus genetiniam konsultavimui. Šio drabo tikslas- įvertinti chromosomų struktūros persitvarkymų, nustatytų VUL SK MGC 2002 – 2008 m., įvairovę ir genetinę jų reikšmę. Tam, kad būtų įvertinta chromosomų struktūros persitvarkymų įvairovę, buvo analizuojami 2002-2008 metais atlikti kariotipo tyrimai. Remiantis rezultatais galima teigti, kad dažniausias chromosomų struktūros pakitimas yra reciprokinė translokacija, kuri dažniausiai lemia nevaisingumą bei savaiminius persileidimus. Didžiausia chromosomų struktūros pakitimų įvairovė nustatyta X chromosomoje.Rutininė citogenetinė kariotipo analizė yra svarbi ir tais atvejais, kai atliekamas FISH tyrimas naudojant tam tikrai genetinei sričiai specifinį žymenį, kadangi skirtingi chromosomų struktūros persitvarkymai gali lemti panašų fenotipą. / Chromosome structural rearrangements could cause various human health problems. Even Down’s or Turner’s syndromes, which are usually determined by chromosome number change, in some cases could be caused by chromosome structure abnormalities. Structure rerrangements of autosomes, depending on whether it is balanced origin or not, are responsible for various dysmorphic abnormalities or fertility problems. Chromosome breakpoints can occur in any part of chromosome and form any type of rearrangement, but only part of them could be compatible with vital functions and detected postnatally. Chromosome structural rearrangements in many cases are unique and only particular ones are more common. The objective of this work was to assess the diversity of chromosome structural rearrangements and their implication to the human genetic. Cytogenetic analysis of karyotype was performed using G-banding and FISH techniques. Cytogenetic analyses of 76 patients using routine cytogenetic analysis and 20 patients using FISH method have been performed. In order to assess the variety of chromosome structural rearrangements, the results of karyotype analyses performed in Department of Human and Medical Genetics, Faculty of Medicine, Vilnius University during the period of 2002–2008 were reviewed. On the basis of obtained results a conclusion can be drawn that translocation is the most frequent chromosome structure rearrangement type, comprising 44,3% of all our cases. X chromosome is the most... [to full text]
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The Beckmann rearrangement involving optically active radicals ...Wallis, Everett Stanley, January 1926 (has links)
Thesis (Ph. D.)--Princeton University, 1925.
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Novel Catalytic Reactions Enabled by Metal-Induced Boronate Rearrangement:Law, Chunyin Marshall January 2020 (has links)
Thesis advisor: James P. Morken / This dissertation will discuss the development of three methodologies that take advantage of the intrinsic reactivity of organoboron “ate” complex to undergo boronate rearrangement. The first chapter will describe a nickel-catalyzed conjunctive cross-coupling reaction between 9-BBN boranes and aryl halides. This process provides secondary organoboranes enantioselectively from readily available alkenyl starting materials. The second chapter will describe the development of conjunctive cross-coupling between 9-BBN boranes and acyl electrophiles. We will highlight its unique value in the syntheses of β-hydroxyl carbonyls and show that this reaction is complementary to the aldol reaction. In the third and last chapter of this manuscript, we report the conjunctive crosscoupling reaction of simple achiral borylenynes towards the enantio- and diastereoselective synthesis of α-borylallenes, which provides α-allenols upon oxidative workup. / Thesis (PhD) — Boston College, 2020. / Submitted to: Boston College. Graduate School of Arts and Sciences. / Discipline: Chemistry.
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Studies toward the synthesis of (+)-jasplakinolideBroadbelt, Brian January 1995 (has links)
No description available.
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Synthesis of unsymmetrically substituted benzenesOxford, Anona June January 1989 (has links)
No description available.
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1. Highly diastereoselective asymmetric thio-claisen rearrangement ; 2. Total synthesis of strychnos alkaloids /He, Shuwen. January 2001 (has links)
Thesis (Ph. D.)--University of Chicago, Dept. of Chemistry, June 2001. / Includes bibliographical references. Also available on the Internet.
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[2,3]-sigmatropic rearrangements of allylic aminesMiddleton, Mark L. January 1998 (has links)
No description available.
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Rearrangements in the indolo[2,3-b]quinoline system : a novel approach to the synthesis of perophoramidine and the communesins /Voûte, Nicholas. January 2008 (has links)
Thesis (Ph.D.) - University of St Andrews, January 2008. / Restricted until 15th January 2009.
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Stereoelectronic controls in the preparation of 1-benzyl-l, 2, 4, 5-tetrahydro-(3H)-2-benzazepin-3-ones via Beckmann rearrangement /Silvary, Sunil Raj, January 2007 (has links)
Thesis (M.S.) in Chemistry--University of Maine, 2007. / Includes vita. Includes bibliographical references (leaves 37-39).
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