Studies towards the synthesis of hyperireflexolide A
The first approach to hyperireflexolide A, based on the synthesis of γ-lactone-fused cyclopentane , a functionalized key intermediate, is presented. Compound is involved in hydrolysis, α-allylation at C-8 and α-methylation at C-10 stereoselectively from the convex face. Then it is subjected to cross...
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Veröffentlicht in: | Beilstein journal of organic chemistry 2018-08, Vol.14 (1), p.2106-2111 |
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Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | The first approach to hyperireflexolide A, based on the synthesis of γ-lactone-fused cyclopentane
, a functionalized key intermediate, is presented. Compound
is involved in hydrolysis, α-allylation at C-8 and α-methylation at C-10 stereoselectively from the convex face. Then it is subjected to cross metathesis to give α
β-unsaturated ketone
as precursor in the total synthesis of hyperireflexolide A. |
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ISSN: | 1860-5397 2195-951X 1860-5397 |
DOI: | 10.3762/bjoc.14.185 |