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New methods for the synthesis of fused ring structuresGutsche, C. David January 1947 (has links)
Thesis (Ph. D.)--University of Wisconsin--Madison, 1947. / Typescript. Vita. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references (leaves 167-171).
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I. Über Indoxazen ; II. Constitutionsbestimmungen in der Thiophenreihe Inaugural-dissertation ... /Marcusson, J. January 1894 (has links)
Thesis--Universität Heidelberg, 1894.
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'Coarctate' cyclizations : applications to heterocycle synthesis /Shirtcliff, Laura Donnell, January 2006 (has links)
Thesis (Ph. D.)--University of Oregon, 2006. / Typescript. Includes vita and abstract. Includes bibliographical references (leaves 336-357). Also available for download via the World Wide Web; free to University of Oregon users.
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Pyrolysis and synthesis of cyclic compounds related to cyclohexene ...Stallbaumer, Adrian Lawrence, January 1942 (has links)
Thesis (Ph. D.)--Catholic University of America, 1942. / Reproduced from type-written copy. "Literature cited": p. 41-43.
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Synthesis of aza-bicyclic compounds via palladium-catalyzed cascade cyclization reactionsLo, Kai-yip., 羅啟業. January 2012 (has links)
A palladium-catalyzed oxidative cascade cyclization reaction has been developed to prepare pyrrolizidine and indolizidine derivatives from simple aliphatic alkenyl amides 2.1ak in one step in moderate to good yields, using Pd(TFA)2 as the catalyst and molecular oxygen (1 atm) as a green oxidant. This cascade cyclization can also proceed for ring-containing unsaturated amides 2.1ln to afford azatricyclic systems.
Palladium(II)-catalyzed dehydrohalogenation cascade cyclization reactions have been developed to synthesize polycyclic pyrrolizidine derivatives from iodoalkenylanilides 4.1ai in satisfactory to excellent yields under mild conditions. This reaction produces two stereocenters in one step and only one single diastereomer was obtained in the cyclization of 4.1. The reaction is proposed to proceed through an organopalladium(IV) species, formed by oxidative addition after the aminopalladation. This organopalladium(IV) species then undergoes reductive elimination to give the cyclized product. This cyclization is a fast and efficient way to construct natural alkaloids that contain pyrrolizidine or indolizidine cores. / published_or_final_version / Chemistry / Doctoral / Doctor of Philosophy
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Development of synthetic methods for the preparation of cyclobutenes and glycopeptidesOwino, Norbert Oduor. January 2004 (has links)
Thesis (Ph. D.)--State University of New York at Binghamton, Chemistry Department, 2004. / Includes bibliographical references.
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Silver catalyzed enyne cyclization reactionsChen, Haoguo., 陳浩國. January 2009 (has links)
published_or_final_version / Chemistry / Doctoral / Doctor of Philosophy
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Synthesis of amino acids by metal-catalysed reactionsTeoh, Euneace Ching Mei January 2004 (has links)
Abstract not available
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Silver catalyzed enyne cyclization reactionsChen, Haoguo. January 2009 (has links)
Thesis (Ph. D.)--University of Hong Kong, 2009. / Includes bibliographical references (leaves 115-116). Also available in print.
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Ring-closing metathesis for the synthesis of carbocyclic and heterocyclic intramolecular Baylis-Hillman adductsSong, Eunho. Krafft, Marie E. January 2005 (has links)
Thesis (M.S.)--Florida State University, 2005. / Advisor: Dr. Marie E. Krafft, Florida State University, College of Arts and Sciences, Dept. of Chemistry and Biochemistry. Title and description from dissertation home page (viewed Sept. 19, 2005). Document formatted into pages; contains 147 pages. Includes bibliographical references.
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