4.4 Article

Synthesis of bhimamycin B based on oxidative rearrangement of 4-acetylnaphtho[1,2-b]furan-5-ol to naphtho[2,3-c]furan-4,9-dione

Journal

TETRAHEDRON LETTERS
Volume 46, Issue 23, Pages 3997-4000

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2005.04.037

Keywords

bhimamycin B; iodosobenzene diacetate; naphtho[2,3-c]furan

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The first total synthesis of bhimamycin B, a novel member of naphtho[2,3-c]furan quinone antibiotics, was achieved by oxidative skeletal rearrangement of 4-acetylnaphtho[1,2-b]furan-5-ol. (c) 2005 Elsevier Ltd. All rights reserved.

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