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Studies toward the total synthesis of pseudolaric acid A /Chen, Bin, January 2001 (has links)
Thesis (Ph. D.)--University of Hong Kong, 2001. / Includes bibliographical references (leaves 150-158).
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Studies toward the total synthesis of pseudolaric acid B via an improved carbene cyclization cycloaddition cascade strategyLi, Baojian, 李保健 January 2014 (has links)
published_or_final_version / Chemistry / Doctoral / Doctor of Philosophy
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I. Crystal structure of a norditerpene dilactone; II. CMR spectra of analgesicsChou, Paul chi-Chou, 1940- January 1976 (has links)
No description available.
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Some stereochemical and synthetic studies in serrulatane diterpenoid chemistry / by Linda Marie CowinCowin, Linda Marie January 1992 (has links)
Bibliography: leaves 141-144 / vii, 144 leaves : ill ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / Thesis (Ph.D.)--University of Adelaide, Dept. of Organic Chemistry, 1993?
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Some stereochemical and synthetic studies in serrulatane diterpenoid chemistry /Cowin, Linda Marie. January 1992 (has links) (PDF)
Thesis (Ph. D.)--University of Adelaide, Dept. of Organic Chemistry, 1993? / Includes bibliographical references (leaves 141-144).
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The total syntheses of jatrophatrione, citlalitrione, and sclerophytin A studes toward the enantioselective synthesis of fomannosin; photochemical rearrangement of 4-methoxy-4-vinyl-2-cyclopentenones /Yang, Jiong, January 2003 (has links)
Thesis (Ph. D.)--Ohio State University, 2003. / Title from first page of PDF file. Document formatted into pages; contains xx, 293 p. : ill. Advisor: Leo A. Paquette, Department of Chemistry. Includes bibliographical references (p. 88-101).
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Estudos sobre alcaloides diterpenicosOrtellado, Maria Amelia de Almeida 15 July 2018 (has links)
Orientador : Anita Jocelyne Marsaioli / Dissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Quimica / Made available in DSpace on 2018-07-15T02:42:03Z (GMT). No. of bitstreams: 1
Ortellado_MariaAmeliadeAlmeida_M.pdf: 5211680 bytes, checksum: 0c3d14e3376d2553756adfe99391dc49 (MD5)
Previous issue date: 1986 / Mestrado
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Studies toward the total synthesis of pseudolaric acid AChen, Bin, 陳斌 January 2001 (has links)
published_or_final_version / Chemistry / Doctoral / Doctor of Philosophy
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Synthetic approach to bonandiol and hyperforin.Heidt, Philip Conrad. January 1988 (has links)
The enantioselective approach to bonandiol, also known as magydardiendiol, has utilized two novel synthetic methodologies. The first is the diastereoselective cyclopropanation of a homochiral eneketal prepared from (2R,3R)- or (2S,3S)-2,3-butanediol and possessing C₂ symmetry. Simmons-Smith cyclopropanation gave good diastereoselectivity (69-75%) in addition to excellent amounts of monocyclopropanated material obtained (90-96%). The second method utilized is the nickel acetylacetonate catalyzed coupling of dimethylzinc to a sterically hindered cyclic β-keto enolphosphate in 76-92% yield. This approach to the A ring of hyperforin starting from commercially available citral allows for the introduction of all but one isoprenyl appendage.
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Synthetic studies towards furanocembranes and pseudopteranesGonzalez Lopez de Turiso, Felix January 2002 (has links)
No description available.
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