Synthetic studies on borrelidin: enantioselective synthesis of the C1-C12 fragment.
نویسندگان
چکیده
[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.
منابع مشابه
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عنوان ژورنال:
- Organic letters
دوره 5 10 شماره
صفحات -
تاریخ انتشار 2003