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Macrocyclic natural products ring-closing metathesis

Synthesis of Natural Products Containing Macrocycles by Alkene Ring-closing Metathesis... [Pg.149]

Grasillas, A. Perez-Castells, J. Macrocyclization by ring-closing metathesis in the total synthesis of natural products Reaction conditions and limitations. Angew. Chem. Int. Ed. 2006,45, 6086-6101. [Pg.259]

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]

Macrocyclization by ring-closing metathesis in the total synthesis of natural products 06AG(E)6086. [Pg.34]

Synthesis of macrocyclic compounds including natural products by ring closing metathesis 07COC1339. [Pg.35]

Gradihas A, CasteUs JP. Macrocyclization by Ring-Closing Metathesis in the Total Synthesis of Natural Products Reaction Conditions and Limitations. Angew Chem Int Ed. 2006 45(37) 6086-6101. [Pg.185]


See other pages where Macrocyclic natural products ring-closing metathesis is mentioned: [Pg.46]    [Pg.69]    [Pg.62]    [Pg.201]    [Pg.243]    [Pg.38]    [Pg.244]    [Pg.623]    [Pg.374]    [Pg.31]    [Pg.194]    [Pg.201]    [Pg.1023]    [Pg.1039]    [Pg.389]    [Pg.686]    [Pg.185]    [Pg.263]    [Pg.176]    [Pg.17]    [Pg.41]    [Pg.149]    [Pg.270]    [Pg.272]    [Pg.273]   


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Macrocycles rings

Macrocyclic Ring Closing Metathesis

Macrocyclic natural

Macrocyclic natural product

Macrocyclic ring

Ring metathesis

Ring products

Ring-closed

Ring-closing

Ring-closing metatheses

Ring-closing metathesi

Ring-closing metathesis macrocycles

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