Towards the Total Synthesis of Vibsanin E, 15-O Methylcyclovibsanin B, 3-Hydroxyvibsanin E, Furanovibsanin A, and 3-O Methylfuranovibsanin A
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Authors
Schwartz, Brett
Tilly, David P
Heim, Ralf
Wiedemann, Stefan
Williams, Craig
Bernhardt, Paul
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Wiley-VCH Verlag GMBH
Abstract
Studies detailing synthetic approaches to a variety of biosynthetically related vibsanin-type diterpenes (i.e. vibsanin E, 15-O-methylcyclovibsanin B, 3-hydroxy-vibsanin E, furanovibsanin A, and 3-O-methylfuranovibsanin A) are discussed. Biogenetically modelled approaches are coupled with an investigation of classical and modern six- to seven-membered ring-expansion protocols, which gain access to the central core of these natural products.
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European Journal of Organic Chemistry
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2037-12-31