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Synthèses d'analogues thiophéniques des paullones, agents antitumoraux potentielsMigianu, Evelyne. Kirsch, Gilbert. January 2008 (has links) (PDF)
Reproduction de : Thèse doctorat : Chimie moléculaire : Metz : 2002. / Titre provenant de l'écran-titre. Notes bibliographiques.
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Novel synthesis of 3,4-fused indolesHubbard, Jeremiah W. January 2001 (has links)
Thesis (M.S.)--West Virginia University, 2001. / Title from document title page. Document formatted into pages; contains xi, 70, 76 p. : ill. Includes abstract. Includes bibliographical references (p. 67-70).
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Structures of indole alkaloids from Strychnos angustiflora.Au, Tak-yan, Francis. January 1973 (has links)
Thesis (M. Sc.)--University of Hong Kong, 1973.
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Structures of indole alkaloids from Strychnos angustifloraAu, Tak-yan, Francis, 區德仁 January 1973 (has links)
(Uncorrected OCR)
�Abstract of thesis entitled "Structures of Indole
Alkaloids from Strychnos angustiflora" submitted by ~
AU Tak-yan, Francis for the degree of Master of Science at the University of Hong Kong in March 1973.
- i -
ABSTRACT
From the leaves of Strychnos angustiflora Benth,three orange-coloured alkaloids angustoline, angus tine and angustidine have been isolated in low yield.
/
Molecular formulae and electronic spectra
indicate that all three alkaloids have the same highly
I
conjugated polycyclic skeleton.
Structure~ shown below
\
are proposed�
H
Alkaloid Formula Rl R2
Angustoline C2'OH1702N3 CH(OH)CH3 H
Angustine C20'H1SON3 CH=CH2 !
Angustidine Cl9H1SON3 H CH3 The major alkaloid, angustoline, is monoacidic and the hydrochloride-and the picr~te sa~ts have been prepared.
- ii -
The presence of a l-hydroxyethyl side chain shown by n.m.r. has been confir.med by acetylation to g~ve an
/
acetate.
Chemical correlation between angustoline and angustine has been achieved in two ways. Firstly, the
former was converted to the latter 'by acidic catalysed dehydration � Secondly, an~ustoline or its acetate on heating with collidine yielded dihydroangustine, also obtained from angustine by hydrogenation.
Arguments are presented for the structures of the three alkaloids, based substantially on n.m.r. data
(including long-range coupling and N.O.E. data) and biogenetic considerations.
I i
The three alkaloids are postulated to be derived biogenetically from vincoside, the fused pyridine ring being formed via opening of the iridoid glycoside ring by ammonia (or equivalent). / abstract / toc / Chemistry / Master / Master of Science
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Synthetic study of seco-yuehchukene and inverto-yuehchukene李輝途, Lee, Victor. January 1987 (has links)
published_or_final_version / Chemistry / Master / Master of Philosophy
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A general synthetic route to Yuehchukene analogues via 7alpha-methoxycarbonyl-9-methyl-6-oxo-5,6,6abeta,7betaB,8,10aB-hexahydroindeno [2,1-b] indole, and related studies on 1-methoxyindole黃子達, Wong, Tze-tat, Edward. January 1992 (has links)
published_or_final_version / Chemistry / Doctoral / Doctor of Philosophy
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Total synthesis of (+)-madindoline A and (+)- madindoline B / Total synthesis of plus-madindoline A and plus- madindoline BWan, Lifeng January 2006 (has links)
Thesis (M.S.)--University of Hawaii at Manoa, 2006. / Includes bibliographical references (leaves 83-86). / x, 86 leaves, bound ill. 29 cm
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Synthetical experiments related to the indole alkaloids / by David Roland Liljegren.Liljegren, David Roland January 1962 (has links)
Typewritten / 153 leaves / 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, 1962
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The synthesis of 3-ethoxyindoles, koniamborine, salviadione and studies toward fistulosin utilizing palladium-catalyzed reductive N-heteroannulationClawson, Ronald W. January 2007 (has links)
Thesis (Ph. D.)--West Virginia University, 2007. / Title from document title page. Document formatted into pages; contains xxiv, 282 p. : ill. (some col.). Includes abstract. Includes bibliographical references (p. 166-179).
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Isolation of a piperitol epimer, and Studies on the Fischer indole synthesis /Barnes, Charles Stalley. January 1950 (has links) (PDF)
Thesis (M.S) -- University of Adelaide, 1950. / Typewritten copy.
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