Journal
TETRAHEDRON LETTERS
Volume 47, Issue 13, Pages 2099-2102Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2006.01.130
Keywords
clavosolides; clavosolide A; epoxide opening; 2-methyl-1.3-diol; diolide
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The total synthesis of clavosolide A, employing a radical-mediated route to build its substituted tetrahydropyran unit, a Yamaguchi reaction to construct the diolide aglycon and the Schmidt method for the final glycosidation step, revealed that the reported structure is an isomer of the natural product. (c) 2006 Elsevier Ltd. All rights reserved.
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