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Cascade reactions transannular Michael reaction

Norzoanthamine is a heptacychc alkaloid originally isolated from marine zoanthids. In addition to its complex molecular structure, norzoanthamine is well-known for its potent antiosteoporotic activity. In their studies toward the total synthesis of norzoanthamine, Yang and co-workers developed a 12-step enantioselective synthesis of the highly functionalized and stereochemically complex ABC ring system. A transannular Michael reaction cascade was... [Pg.565]

SCHEME 20.27. The transannular Michael reaction cascade in the total synthesis of salvinorin A. [Pg.565]

SCHEME 20.28. The norzoanthamine ABC ring system by a transannular Michael reaction cascade. [Pg.566]

Xue H, Yang J, Gopal P. Toward the synthesis of norzoanth-amine building carbocyclic core by a transannular Michael reaction cascade. Org. Lett. 2011 13 5696-5699. [Pg.578]

For a recent study of a transannular Michael reaction cascade Xue H, Gopal P, Yang J. Stereochemical study of a transannular Michael reaction cascade. J. Org. Chem. 2012 77 8933 945. [Pg.579]

A transannular Michael reaction cascade with both (E,Z)- and ( , )-macrocyclic-1,7-bis-enones (307) has been reported to afford triyclic products (308) with excellent diastereoselectivity. By contrast, (Z,E)- and (Z,Z)-macrocyclic lactones failed to cyclize, apparently due to an unfavourable geometry. [Pg.385]


See other pages where Cascade reactions transannular Michael reaction is mentioned: [Pg.147]    [Pg.147]    [Pg.565]    [Pg.565]   


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