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frondosin B

 
National Institutes of Health

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2017
2017
Formal syntheses of tetracyclic terpenoids frondosin B and liphagal are described. Both synthetic routes rely on the use of… Expand
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2014
2014
The asymmetric total syntheses of the natural products (+)- and (-)-frondosin B and (+)-frondosin A are reported based on a… Expand
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2014
2014
A recently developed (4+3) cycloaddition between dienes and furfuryl alcohols, as precursors of oxyallyl-type cations, has been… Expand
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2012
2012
A new [4 + 3]-cycloaddition between benzofuran allylic alcohols and dienes, promoted by camphorsulfonic acid, has been identified… Expand
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2004
2004
[reaction: see text] A recently discovered multicomponent coupling reaction is used to give direct access to a late intermediate… Expand
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2001
2001
Two concise syntheses of (+/-)-frondosin B (1), an interleukin-8 receptor antagonist, have been achieved from commercially… Expand
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