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Natural product synthesis carbopalladation

Link JT (2002) Synthesis of Natural Products via Carbopalladation. In Negishi E, de Meijere A (eds) Handbook of Organopalladium Chemistry for Organic Synthesis. Wiley, New York, p 1523... [Pg.45]

Medium sized rings can also be efficiently assembled by carbopalladation reactions. An example from natural product synthesis is the construction of several Amaryllida-cae alkaloids including (-)-pancracine Treatment of aryl bromide 140 with... [Pg.1543]

Asymmetric intramolecular carbopalladation is an effective reaction for producing enantioenriched polycycles. Most examples are intramolecular Heck reactions. One seminal example from natural product synthesis is the 5-exo carbopalladation of eneamide 201 to oxindole 202 (after acid treaunent) from a total synthesis of ( )-physostigmine 203 (Scheme The reaction occurs in 84% yield with 95% ee,... [Pg.1553]


See other pages where Natural product synthesis carbopalladation is mentioned: [Pg.12]    [Pg.22]    [Pg.1272]    [Pg.1523]    [Pg.1525]    [Pg.1525]    [Pg.1526]    [Pg.1527]    [Pg.1529]    [Pg.1531]    [Pg.1533]    [Pg.1535]    [Pg.1537]    [Pg.1539]    [Pg.1541]    [Pg.1543]    [Pg.1545]    [Pg.1547]    [Pg.1548]    [Pg.1549]    [Pg.1551]    [Pg.1553]    [Pg.1555]    [Pg.1557]    [Pg.1560]    [Pg.12]   


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