A new application about 28697-11-2

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Total synthesis of (+)-homopumiliotoxin 223G

A new practical route for the first total synthesis of (+)- homopumiliotoxin 223G is described, in which the palladium-catalyzed carbonylation of the vinyl iodide, leading to efficient construction of the quinolizidine nucleus incorporating the (Z)-alkylidene side chain, is the key strategic clement. Another key feature of this synthesis involves the Lewis acid-induced chelation-controlled propargylation using the allenylsilane with complete diastereoselectivity.

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Reference£º
Piperidine – Wikipedia,
Piperidine | C5H21392N – PubChem