MEDT Study, hemisynthesis via regioselective ring opening of α-Himachalene-Epoxides, ADME survey and docking studies designed to target coronavirus and HIV-1

Ajlaoui, Rahhal El; Raji, Houria; Ouardi, Mahmoud El; Chakroun, Ahmed; Zeroual, Abdellah; Syed, Asad; Bahkali, Ali H.; Elgorban, Abdallah M.; Verma, Meenakshi; Benharref, Ahmed; Varma, Rajender S.

doi:10.1016/j.molliq.2023.123707

Journal of Molecular Liquids

2024

DOI: 10.1016/j.molliq.2023.123707

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MEDT Study, hemisynthesis via regioselective ring opening of α-Himachalene-Epoxides, ADME survey and docking studies designed to target coronavirus and HIV-1

Rahhal El Ajlaoui,

Houria Raji,

Mahmoud El Ouardi

et al.

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Cited by 4 publications

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MEDT Study, hemisynthesis via regioselective ring opening of α-Himachalene-Epoxides, ADME survey and docking studies designed to target coronavirus and HIV-1

Cited by 4 publications

References 40 publications

ADME Study, Molecular Docking, Elucidating the Selectivities and the Mechanism of [4 + 2] Cycloaddition Reaction Between (E)-N ((dimethylamino)methylene)benzothioamide and (S)-3-acryloyl-4-phenyloxazolidin-2-one

ADME Study, Molecular Docking, Elucidating the Selectivities and the Mechanism of [4 + 2] Cycloaddition Reaction Between (E)-N ((dimethylamino)methylene)benzothioamide and (S)-3-acryloyl-4-phenyloxazolidin-2-one

Polygonum minus: A tropical medicinal herb with vast applications in food, agricultural, and medicinal fields

Synthesis, X-ray analysis, and antiviral evaluation of allohimachalol: Insights into stereoselectivity in epoxidation

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