Eco-friendly synthesis, physicochemical studies, biological assay and molecular docking of steroidal oxime-ethers
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Bibliographic citation
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Eco-friendly synthesis, physicochemical studies, biological assay and molecular docking of steroidal oxime-ethers ; Vol. 14, 2015
EXCLI journal ; Vol. 14, 2015
- Classification
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Medizin, Gesundheit
- Creator
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Alam, Mahboob
Lee, Dong-Ung
- Handle
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2003/34042
- URN
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urn:nbn:de:101:1-201606013090
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:52 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Alam, Mahboob
- Lee, Dong-Ung
Other Objects (12)
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Functionalized Cyclopentenones and an Oxime Ether as Antimicrobial Agents
SYNTHESIS OF NEW 2-ARYL-4H-4-OXO-1-BENZOPYRAN OXIME ETHERS
Free Radical Acylation Approaches of C-H Bonds with 2-Chloroethylsulfonyl Oxime Ethers
N-Heterocycles from Oxime and Oxime O-Benzyl Ethers via Electrophile Induced - Ring Formation. Route to Cyclic and Bicyclic Amine and Hydroxylamine
Study of the Room‐Temperature Synthesis of Oxime Ethers by using a Super Base
Ueber Oxime unsymmetrischer Ketone
Oxime der Violerythrin-Endgruppe
Cyclopentyl Methyl Ether: An Elective Ecofriendly Ethereal Solvent in Classical and Modern Organic Chemistry
Mild reductive rearrangement of oximes and oxime ethers to secondary amines with hydrosilanes catalyzed by B(C6F5)3
Study of the Mechanism of 7‐ exo ‐ trig Cyclizations of Aryl, Vinyl, and Alkyl Radicals on Oxime Ethers
Vicinal difunctionalization of alkenes by four-component radical cascade reaction of xanthogenates, alkenes, CO, and sulfonyl oxime ethers
Cu-Catalyzed Introduction of Oxime Ethers into Peptides
Functionalized Cyclopentenones and an Oxime Ether as Antimicrobial Agents
SYNTHESIS OF NEW 2-ARYL-4H-4-OXO-1-BENZOPYRAN OXIME ETHERS
Free Radical Acylation Approaches of C-H Bonds with 2-Chloroethylsulfonyl Oxime Ethers
N-Heterocycles from Oxime and Oxime O-Benzyl Ethers via Electrophile Induced - Ring Formation. Route to Cyclic and Bicyclic Amine and Hydroxylamine
Study of the Room‐Temperature Synthesis of Oxime Ethers by using a Super Base
Ueber Oxime unsymmetrischer Ketone
Oxime der Violerythrin-Endgruppe
Cyclopentyl Methyl Ether: An Elective Ecofriendly Ethereal Solvent in Classical and Modern Organic Chemistry
Mild reductive rearrangement of oximes and oxime ethers to secondary amines with hydrosilanes catalyzed by B(C6F5)3
Study of the Mechanism of 7‐ exo ‐ trig Cyclizations of Aryl, Vinyl, and Alkyl Radicals on Oxime Ethers
Vicinal difunctionalization of alkenes by four-component radical cascade reaction of xanthogenates, alkenes, CO, and sulfonyl oxime ethers
Cu-Catalyzed Introduction of Oxime Ethers into Peptides
Functionalized Cyclopentenones and an Oxime Ether as Antimicrobial Agents
SYNTHESIS OF NEW 2-ARYL-4H-4-OXO-1-BENZOPYRAN OXIME ETHERS
Free Radical Acylation Approaches of C-H Bonds with 2-Chloroethylsulfonyl Oxime Ethers
N-Heterocycles from Oxime and Oxime O-Benzyl Ethers via Electrophile Induced - Ring Formation. Route to Cyclic and Bicyclic Amine and Hydroxylamine
Study of the Room‐Temperature Synthesis of Oxime Ethers by using a Super Base
Ueber Oxime unsymmetrischer Ketone
Oxime der Violerythrin-Endgruppe
Cyclopentyl Methyl Ether: An Elective Ecofriendly Ethereal Solvent in Classical and Modern Organic Chemistry
Mild reductive rearrangement of oximes and oxime ethers to secondary amines with hydrosilanes catalyzed by B(C6F5)3
Study of the Mechanism of 7‐ exo ‐ trig Cyclizations of Aryl, Vinyl, and Alkyl Radicals on Oxime Ethers