4.4 Article

Total synthesis and absolute stereochemistry of (+)-batzellaside B and its C8-epimer, a new class of piperidine alkaloids from the sponge Batzella sp.

Journal

TETRAHEDRON LETTERS
Volume 52, Issue 11, Pages 1173-1175

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2011.01.018

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Funding

  1. Ministry of Education, Culture, Sports, Science and Technology, Japan
  2. Grants-in-Aid for Scientific Research [22550032] Funding Source: KAKEN

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The first total synthesis of (+)-batzellaside B and its C8-epimer was completed from a known L-arabinose-derived tribenzyl ether ill 22 steps with overall yields of 3.9% and 5.4%, respectively. The absolute configuration of (+)-batzellaside B was unambiguously determined to be 1S,3S,4S,5R,8S by the Mosher analysis of a synthetic intermediate prepared through a separate route. (C) 2011 Elsevier Ltd. All rights reserved.

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