Synthesis of the Originally Proposed Structures of Elatenyne and an Enyne from Laurencia Majuscula
Overview
Chemistry
Affiliations
A bidirectional synthesis of the originally proposed structures for the natural products elatenyne and a chloroenyne from Laurencia majuscula is described along with a reassessment of the structures of the halogenated enynes based upon a 13C NMR chemical shift/structure correlation.
Stereoselective total synthesis of (3)- and (3)-elatenynes.
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