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Macrocyclic natural products olefin ring-closing metathesis

In the ring-closing metathesis reaction (RCM), a diene is allowed to undergo intramolecular olefin metathesis to give a cyclic alkene and ethylene the latter is removed to drive the equilibrium forward. The RCM has quickly been adopted as a premier method for preparing macrocyclic natural products. [Pg.303]

The epothilones comprise an important set of natural products that were discovered at a time contemporary with the development of ring-closing olefin metathesis. These materials are 16-membered ring compounds containing an alkene in the macrocycle or an epoxide that can be generated from the alkene. A conventional retrosyntlietic analysis... [Pg.1024]


See other pages where Macrocyclic natural products olefin ring-closing metathesis is mentioned: [Pg.69]    [Pg.201]    [Pg.194]    [Pg.1023]    [Pg.1039]    [Pg.41]    [Pg.270]    [Pg.272]    [Pg.273]    [Pg.325]    [Pg.369]    [Pg.257]    [Pg.11]    [Pg.224]    [Pg.475]   
See also in sourсe #XX -- [ Pg.723 ]




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Macrocycles rings

Macrocyclic Ring Closing Metathesis

Macrocyclic natural

Macrocyclic natural product

Macrocyclic ring

Macrocyclization olefin metathesis

Olefin metathesis

Olefin ring-closing

Olefine metathesis

Ring metathesis

Ring products

Ring-closed

Ring-closing

Ring-closing metatheses

Ring-closing metathesi

Ring-closing metathesis macrocycles

Ring-closing olefin metathesis

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