One-step, stereoselective synthesis of octahydrochromanes <i>via</i> the Prins reaction and their cannabinoid activities.

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第一作者： Shuneize,Slater

第一单位： National Center for Natural Products Research, School of Pharmacy, The University of Mississippi, University, MS, 38677, USA.

作者： Shuneize,Slater ^[1] ; Pradeep B,Lasonkar ^[1] ; Saqlain,Haider ^[1] ; Moneerah J,Alqahtani ^[2] ; Amar G,Chittiboyina ^[1] ; Ikhlas A,Khan ^[3]

作者单位： National Center for Natural Products Research, School of Pharmacy, The University of Mississippi, University, MS, 38677, USA. ^[1] Division of Pharmacognosy, Department of BioMolecular Sciences, School of Pharmacy, The University of Mississippi, University, MS, 38677, USA. ^[2] National Center for Natural Products Research, School of Pharmacy, The University of Mississippi, University, MS, 38677, USA.;Division of Pharmacognosy, Department of BioMolecular Sciences, School of Pharmacy, The University of Mississippi, University, MS, 38677, USA. ^[3]

关键词 Cannabinoid receptors Enantioselectivity Octahydrochromene Prins cyclization

DOI 10.1016/j.tetlet.2018.01.040

PMID 29880989

发布时间 2024-11-08

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