4.4 Article

Stereoselective synthesis of the C21-C27 fragment of the phorboxazoles

Journal

TETRAHEDRON LETTERS
Volume 44, Issue 26, Pages 4933-4935

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0040-4039(03)01099-2

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A stereoselective synthesis of the C21-C27 fragment of phorboxazoles A and B was achieved in 12 linear steps via an intramolecular cyclization induced by mercury acetate, to afford a functionalized tetrahydropyran. (C) 2003 Elsevier Science Ltd. All rights reserved.

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