Published on WebAsymmetric Synthesis of Salvinorin A, A Potent K Opioid Receptor Agonist Jonathan R. Scheerer, Jonathan F. Lawrence, Grace C. Wang, and David A. Evans* Department of Chemistry and Chemical Bi

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Date: 2007-10-09 12:11:18 Chemistry Organic chemistry Total synthesis Diterpenes Salvinorin Aldol reaction Heinz Falk Endiandric acid C		Published on WebAsymmetric Synthesis of Salvinorin A, A Potent K Opioid Receptor Agonist Jonathan R. Scheerer, Jonathan F. Lawrence, Grace C. Wang, and David A. Evans* Department of Chemistry and Chemical Bi Add to Reading List Source URL: evans.rc.fas.harvard.edu Download Document from Source Website File Size: 86,43 KB Share Document on Facebook

	Published on WebAsymmetric Synthesis of Salvinorin A, A Potent K Opioid Receptor Agonist Jonathan R. Scheerer, Jonathan F. Lawrence, Grace C. Wang, and David A. Evans* Department of Chemistry and Chemical Bi DocID: 1rohR - View Document
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