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  1. Article ; Online: Synthesis of A-ring quinolones, nine-membered oxolactams and spiroindoles by oxidative transformations of 2,3-indolotriterpenoids.

    Khusnutdinova, Elmira F / Kazakova, Oxana B / Lobov, Alexander N / Kukovinets, Olga S / Suponitsky, Kyrill Yu / Meyers, Craig B / Prichard, Mark N

    Organic & biomolecular chemistry

    2018  Volume 17, Issue 3, Page(s) 585–597

    Abstract: This paper describes an access to new nitrogen-containing heterocyclic triterpenoids by the reaction of 2,3-indolotriterpenoids with ozone and dimethyldioxirane. The oxidation of indolo-fused 28-oxo-allobetulin or methyl platanoate with ozone led to a ... ...

    Abstract This paper describes an access to new nitrogen-containing heterocyclic triterpenoids by the reaction of 2,3-indolotriterpenoids with ozone and dimethyldioxirane. The oxidation of indolo-fused 28-oxo-allobetulin or methyl platanoate with ozone led to a mixture of a quinolone as the major product and a nine-membered 2,3-seco-2-oxolactam and three different types of spiroindoles as byproducts. The formation of quinolone and 2,3-seco-2-oxolactam derivatives could be explained by the standard 1,3-dipolar cycloaddition of ozone to the C2(3)-double bond of the triterpene core similar to the products observed in the ozonolysis of indoles in the Witkop-Winterfeldt oxidation (WWO). The formation of spiroindoles was unexpected and could be explained through the 1,2-cycloaddition of ozone to the C2(3)-double bond with consecutive intramolecular rearrangements of the 2,3-epoxy-intermediate. These spiroindoles seem to be novel structures observed in the WWO reaction. The formation of only two isomeric triterpene spiroindolinones was achieved by the oxidation of 2,3-indolo-28-oxo-allobetulin with dimethyldioxirane that could be explained by the rearrangement of the 2,3-epoxy-intermediate. 19β,28-Epoxy-18α-olean-28-oxo-2-nor-2,3-4'(1H)-quinolone was the most active against HPV-11 with EC50 0.45 μM and SI50 322 in a primary assay and SI90 < 10 against HPV-16 in a secondary assay. The oxidative transformations of indolotriterpenoids have great potential for further modifications towards the preparation of new biologically active compounds.
    Language English
    Publishing date 2018-12-21
    Publishing country England
    Document type Journal Article
    ZDB-ID 2097583-1
    ISSN 1477-0539 ; 1477-0520
    ISSN (online) 1477-0539
    ISSN 1477-0520
    DOI 10.1039/c8ob02624f
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Stereospecific Oxidation of Diacetoxyheterobetulin with Ozone and Dimethyldioxirane.

    Khusnutdinova, El'mira F / Medvedeva, Natalya I / Kazakov, Dmitri V / Kukovinets, Olga S / Lobov, Alexander N / Suponitsky, Kirill Yu / Kazakov, Oxana B

    Natural product communications

    2016  Volume 11, Issue 4, Page(s) 449–452

    Abstract: Stereospecific oxidation of diacetoxyheterobetulin with ozone and dimethyldioxirane led to 3β,28-diacetoxy-18α,19βH-urs-20α,21α-epoxide with yields of 79% and 87%, respectively. Oxidation with ozone was not selective and gave two minor products ... ...

    Abstract Stereospecific oxidation of diacetoxyheterobetulin with ozone and dimethyldioxirane led to 3β,28-diacetoxy-18α,19βH-urs-20α,21α-epoxide with yields of 79% and 87%, respectively. Oxidation with ozone was not selective and gave two minor products containing 2lα-hydroxy-20(30)-ene and 21a-hydroxy-20β,28-epoxy-fragments in ring E. The structures of 3β,28-diacetoxy-18α,19βH-urs-20α,21α-epoxide and 3β-diacetoxy-21α-hydroxy-20β,28-epoxy-18α,19βH-ursane were confirmed by X-ray analysis for the first time.
    MeSH term(s) Epoxy Compounds/chemical synthesis ; Epoxy Compounds/chemistry ; Oxidation-Reduction ; Ozone/chemistry ; Stereoisomerism ; Triterpenes/chemical synthesis ; Triterpenes/chemistry
    Chemical Substances 3beta,28-diacetoxy-18alpha,19betaH-urs-20alpha,21alpha-epoxide ; Epoxy Compounds ; Triterpenes ; diacetoxyheterobetulin ; Ozone (66H7ZZK23N) ; dimethyldioxirane (R5RAT196DJ)
    Language English
    Publishing date 2016-04
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 1934-578X
    ISSN 1934-578X
    Database MEDical Literature Analysis and Retrieval System OnLINE

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