Formal convergent synthesis of ivermectin aglycone - A synthetic approach to the C10-C25 subunit of avermectins 2b - École polytechnique Access content directly
Journal Articles Synthesis: Journal of Synthetic Organic Chemistry Year : 2009

Formal convergent synthesis of ivermectin aglycone - A synthetic approach to the C10-C25 subunit of avermectins 2b

Abstract

A convergent, two-fragment synthesis of the C10-C25 northern moiety of avermectins has been developed. Along with our previous work in this area, the present contribution represents a formal synthesis of Ivermectin aglycone. Furthermore, according to a strategy leading to non y-pyranone adducts from, the condensation reaction between acetylacetone dianion and convenient aldehydes, 23-hydroxylated C10-C25 northern building blocks required for the synthesis of the avermectins series 2b were prepared. Subsequent unexpected kinetically favored unnatural (215)-spiro isomers were obtained under mild cyclization conditions.
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hal-00951267 , version 1 (02-03-2014)

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V. Henryon, Jean-Pierre Férézou. Formal convergent synthesis of ivermectin aglycone - A synthetic approach to the C10-C25 subunit of avermectins 2b. Synthesis: Journal of Synthetic Organic Chemistry, 2009, - (20), pp.3477-3487. ⟨10.1055/s-0029-1216954⟩. ⟨hal-00951267⟩
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