A gram-scale route to phlegmarine alkaloids: rapid total synthesis of (-)-cermizine B
The synthesis of the Lycopodium alkaloid ( )-cermizine B (1), which establishes its absolute configuration, is achieved by combining asymmetric organocatalysis and an uninterrupted eight-step reaction sequence, followed by a final reduction step.
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Synthetic and Theoretical Studies for Cyclization Reactions to Form C-C and C-N Bonds [PDF]
, 2018 Natural product total synthesis provides an alternative method for obtaining medicinally relevant compounds in a more efficient process with higher yields than what nature can provide.
Jentsch, Nicholas
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Lyconadins G and H, Two Rare Lyconadin-Type Lycopodium Alkaloids from Lycopodium complanatum. [PDF]
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Antioxidant and cytotoxic activities of three species of tropical seaweeds [PDF]
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Components and Anti-HepG2 Activity Comparison of Lycopodium Alkaloids from Four Geographic Origins. [PDF]
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Carinatines A and B, Lycopodium Alkaloids from Phlegmariurus carinatus. [PDF]
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Effect of protic additives in Cu-catalysed asymmetric Diels-Alder cycloadditions of doubly activated dienophiles: towards the synthesis of magellanine-type Lycopodium alkaloids. [PDF]
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Concise Entries to 4-Halo- and 3-Bromo-4-halo-2-pyridones [PDF]
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Plant carbonic anhydrase-like enzymes in neuroactive alkaloid biosynthesis. [PDF]
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