Novel tandem "Ene-ISMS" methodology. Efficient and versatile assembly of a pseudomonic acid C analogue.

Marko, Istvan;Plancher, JM
(1999) Tetrahedron Letters — Vol. 40, n° 28, p. 5259-5262 (1999)

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Authors
  • Marko, IstvanUCLouvain
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  • Plancher, JM
    Author
Abstract
The pseudomonic acid C analogue 19 can be readily constructed using a novel tandem methodology involving, as a key-step, an ene-reaction followed by a concomitant Intramolecular Silyl-Mediated Sakurai (ISMS) cyclisation. (C) 1999 Elsevier Science Ltd. All rights reserved.
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Marko, I., & Plancher, J. (1999). Novel tandem “Ene-ISMS” methodology. Efficient and versatile assembly of a pseudomonic acid C analogue. Tetrahedron Letters, 40(28), 5259-5262. https://doi.org/10.1016/S0040-4039(99)00996-X (Original work published 1999)