Artigo Revisado por pares

Palladium‐Catalyzed Additions of Alkenyl Epoxides to Pronucleophiles: A Synthesis of the Macrolactam Aglycone of Fluviricin B1

1997; Wiley; Volume: 36; Issue: 13-14 Linguagem: Inglês

10.1002/anie.199714861

ISSN

1521-3773

Autores

Barry M. Trost, Marco Antônio Ceschi, Burkhard König,

Tópico(s)

Asymmetric Synthesis and Catalysis

Resumo

Chirality transfer takes place during the Pd-catalyzed reaction of pronucleophiles with vinyl epoxides bearing and alkyl group at the vinyl terminus. The reaction is ideal to establish remote stereogenic centers. A synthesis of fluviricin B1 aglycone 3 from 1 and 2 illustrates the application of this new strategy for macrolactamization.

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