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- Total synthesis of Sceletium alkaloids (±)-joubertinamine, (±)-epijoubertinamine, (±)-tortuosamine and formal synthesis of (±)-mesembrine, (±)-N-formyltortuosamine. Viraj A. Bhosale, Dattatraya U. Ukale, Suresh B. Waghmode
, New J. Chem.
, 2016
, 40
, 9432
- The structures of partial racemic Sceletium alkaloid A4 and tortuosamine, pyridine alkaloids from Sceletium tortuosum N. E. Br.. F. O. Snyckers, F. Strelow, A. Wiechers
, J. Chem. Soc. D
, 1971
, 1467
- Sceletium alkaloids. Part 7. Structure and absolute stereochemistry of (–)-mesembrane and 3′-methoxy-4′-O-methyljoubertiamine, two minor bases from S. namaquense L. Bolus: X-ray analysis of (–)mesembrane hydrochloride monohydrate. Thomas M. Capps, Karl D. Hargrave, Peter W. Jeffs, Andrew T. McPhail
, J. Chem. Soc., Perkin Trans. 2
, 1977
, 1098
- NS3/4A helicase inhibitory alkaloids from Aptenia cordifolia as HCV target. Asmaa Abo Elgoud Said, Ahmed H. Afifi, Taha F. S. Ali, Mamdouh Nabil Samy, Usama Ramadan Abdelmohsen, Mostafa A. Fouad, Eman Zekry Attia
, RSC Adv.
, 2021
, 11
, 32740
- First enantiocontrolled synthesis of sceletium alkaloid A-4: determination of the absolute configuration. Takashi Kamikubo, Kunio Ogasawara
, Chem. Commun.
, 1998
, 783
- Amaryllidaceae, Sceletium, imidazole, oxazole, thiazole, peptide and miscellaneous alkaloids. John R. Lewis
, Nat. Prod. Rep.
, 2001
, 18
, 95
- Applications of substituted arylacetaldehydes in the total synthesis of mesembrane alkaloids. Part 2. An alternative synthesis of (±)-sceletium alkaloid A4. Craig P. Forbes, George L. Wenteler
, J. Chem. Soc., Perkin Trans. 1
, 1981
, 29
- A review on the assembly of multi-substituted pyridines via Co-catalyzed [2 + 2 + 2] cycloaddition with nitriles. Kaili Cen, Muhammad Usman, Wangzhen Shen, Meijing Liu, Rong Yang, Jinhui Cai
, Org. Biomol. Chem.
, 2022
, 20
, 7391
- Tandem inverse-electron-demand hetero-/retro-Diels–Alder reactions for aromatic nitrogen heterocycle synthesis. Radleigh A. A. Foster, Michael C. Willis
, Chem. Soc. Rev.
, 2013
, 42
, 63
- Amaryllidaceae and Sceletium alkaloids. Zhong Jin
, Nat. Prod. Rep.
, 2003
, 20
, 606