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Synthetic studies on borrelidin: enantioselective synthesis of the C1-C12 fragment
Authors:Vong Binh G  Abraham Sunny  Xiang Alan X  Theodorakis Emmanuel A
Institution:Department of Chemistry and Biochemistry, University of California, San Diego, 9500 Gilman Drive, La Jolla, California 92093-0358, USA.
Abstract:structure: see text] An efficient, enantioselective synthesis of the C1-C12 fragment 2 of borrelidin is presented. Construction of the "skipped" polymethylene chain of 2 was accomplished by iteration of Myers' alkylation, while formation of the C3 stereocenter was achieved by Roush's asymmetric allylboration methodology.
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