001453956 000__ 04597cam\a2200601\i\4500
001453956 001__ 1453956
001453956 003__ OCoLC
001453956 005__ 20230314003454.0
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001453956 007__ cr\cn\nnnunnun
001453956 008__ 230117s2022\\\\sz\a\\\\ob\\\\000\0\eng\d
001453956 019__ $$a1356878026$$a1357017732
001453956 020__ $$a9783031104572$$q(electronic bk.)
001453956 020__ $$a3031104579$$q(electronic bk.)
001453956 020__ $$z3031104560
001453956 020__ $$z9783031104565
001453956 0247_ $$a10.1007/978-3-031-10457-2$$2doi
001453956 035__ $$aSP(OCoLC)1360429668
001453956 040__ $$aGW5XE$$beng$$erda$$epn$$cGW5XE$$dGW5XE$$dYDX$$dEBLCP$$dYDX$$dOCLCQ$$dN$T
001453956 049__ $$aISEA
001453956 050_4 $$aQD421.P76$$bF45 2022
001453956 08204 $$a572/.549$$223/eng/20230117
001453956 1001_ $$aFeineis, Doris,$$eauthor.
001453956 24510 $$aAncistrocladus naphthylisoquinoline alkaloids /$$cby Doris Feineis and Gerhard Bringmann ; A. Douglas Kinghorn, Heinz Falk, Simon Gibbons, Yoshinori Asakawa, Ji-kai Liu, Verena M. Dirsch, editors.
001453956 264_1 $$aCham, Switzerland :$$bSpringer,$$c[2022]
001453956 300__ $$a1 online resource :$$billustrations (black and white, and colour)
001453956 336__ $$atext$$btxt$$2rdacontent
001453956 337__ $$acomputer$$bc$$2rdamedia
001453956 338__ $$aonline resource$$bcr$$2rdacarrier
001453956 4901_ $$aProgress in the chemistry of organic natural products ;$$vvolume 119
001453956 504__ $$aIncludes bibliographical references.
001453956 5050_ $$a1. Introduction -- 2. Naphthylisoquinoline Alkaloids, a Fascinating Class of Axially Chiral Biaryl Natural Products -- 3. Ancistrocladus, a Genus of Woody Lianas of the Monotypic Plant Family Ancistrocladaceae Widely Occurring in India, Sri Lanka, and Southeast Asia -- 4.The Indian Liana Ancistrocladus heyneanus and Ancistrocladus hamatus from Sri Lanka: Early Studies and More Recent Discoveries -- Full Absolute Stereostructures of Naphthylisoquinoline Alkaloids Directly from Crude Extracts: Characterization of New Metabolites from Ancistrocladus griffithii by the HPLC-MS/MS-NMR-ECD Triad -- 6. Ancistrobenomine A, the First Naphthylisoquinoline Alkaloid with a Hydroxymethylene Function at C-3, and Related 5,1'-Coupled Compounds -- 7. Ancistrocladus cochinchinensis from Central Vietnam, a Distinct Ancistrocladus Taxon? Metabolite Pattern und Phylogenetic Relationship to Ancistrocladus aff. tectorius from China -- 8.Widespread Throughout Southeast Asia: Ancistrocladus tectorius, a Rich Source of Unique, Structurally Most Diverse Mono- and Dimeric Naphthylisoquinoline Alkaloids -- 9. Tables of the Naphthylisoquinoline Alkaloids and Related Compounds Isolated from Asian Ancistrocladus Species.
001453956 506__ $$aAccess limited to authorized users.
001453956 520__ $$aThis book describes a unique class of secondary metabolites, the mono- and dimeric-naphthylisoquinoline alkaloids. They exclusively occur in lianas of the palaeotropical Ancistrocladaceae and Dioncophyllaceae plant families. Their unprecedented structures include stereogenic centers and rotationally hindered, and therefore stereogenic, axes. Extended recent investigations on six Ancistrocladus species from Asia, as reported in this contribution, shed light on their fascinating phytochemical productivity, with over 100 intriguing natural products. This high chemodiversity arises from a similarly unique biosynthesis from acetate-malonate units, following a novel polyketidic pathway to plant-derived isoquinoline alkaloids. Some of the compounds show most promising anti-parasitic activities. Additionally, strategies for the regio- and stereoselective total synthesis of the alkaloids, including the directed construction of the chiral axis, are also presented.
001453956 588__ $$aDescription based on print version record.
001453956 650_0 $$aAlkaloids.
001453956 650_0 $$aBotanical chemistry.
001453956 655_0 $$aElectronic books.
001453956 7001_ $$aBringmann, G.$$q(Gerhard),$$eauthor.
001453956 7001_ $$aKinghorn, A. Douglas.$$eeditor.
001453956 7001_ $$aFalk, Heinz,$$d1939-$$eeditor.
001453956 7001_ $$aGibbons, Simon$$c(Professor of medicinal phytochemistry),$$eeditor.
001453956 7001_ $$aAsakawa, Yoshinori.$$eeditor.
001453956 7001_ $$aLiu, Ji-kai.$$eeditor.
001453956 7001_ $$aDirsch, Verena M.$$eeditor.
001453956 77608 $$iPrint version:$$tANCISTROCLADUS NAPHTHOISOQUINOLINE ALKALOIDS.$$d[Place of publication not identified] : SPRINGER INTERNATIONAL PU, 2022$$z3031104560$$w(OCoLC)1329426552
001453956 830_0 $$aFortschritte der Chemie organischer Naturstoffe ;$$v119. Bd.
001453956 852__ $$bebk
001453956 85640 $$3Springer Nature$$uhttps://univsouthin.idm.oclc.org/login?url=https://link.springer.com/10.1007/978-3-031-10457-2$$zOnline Access$$91397441.1
001453956 909CO $$ooai:library.usi.edu:1453956$$pGLOBAL_SET
001453956 980__ $$aBIB
001453956 980__ $$aEBOOK
001453956 982__ $$aEbook
001453956 983__ $$aOnline
001453956 994__ $$a92$$bISE