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Cyclopentanes natural products synthesis, cyclizations

A direct application of the ring-opening reaction of an epoxide by a metal enolate amide for the synthesis of a complex molecule can be found in the synthesis of the trisubstituted cyclopentane core of brefeldin A (Scheme 8.35) [68a]. For this purpose, treatment of epoxy amide 137 with excess KH in THF gave a smooth cyclization to amide 138, which was subsequently converted into the natural product. No base/solvent combination that would effect cyclization of the corresponding aldehyde or ester could be found. [Pg.296]


See other pages where Cyclopentanes natural products synthesis, cyclizations is mentioned: [Pg.407]    [Pg.12]    [Pg.357]    [Pg.12]    [Pg.272]    [Pg.515]    [Pg.236]    [Pg.411]    [Pg.180]    [Pg.371]    [Pg.144]    [Pg.36]    [Pg.1111]   


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Cyclization cyclopentane synthesis

Cyclization natural products synthesis

Cyclization product

Cyclizations synthesis

Cyclopentane

Cyclopentane synthesis

Cyclopentanes

Cyclopentanes synthesis

Natural product synthesis 3 + 2] cyclizations

Natural products, synthesis

Synthesis cyclization

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