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frondosin B

 
National Institutes of Health

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1 relation

Broader (1)

Heterocyclic Compounds, 4 or More Rings

Papers overview

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2017
2017
Platinum-Catalyzed α,β-Unsaturated Carbene Formation in the Formal Syntheses of Frondosin B and Liphagal.
Formal syntheses of tetracyclic terpenoids frondosin B and liphagal are described. Both synthetic routes rely on the use of… Expand
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2016
2016
Approaches to the Synthesis of the Natural Products, Azaphorbol and Frondosin B, via Diazo Decomposition Reactions
 
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2015
2015
Synthesis of Frondosin B Analogs via Rhodium Catalyzed Carbonyl Ylide Cycloaddition
 
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2014
2014
Cyclopropene cycloadditions with annulated furans: total synthesis of (+)- and (-)-frondosin B and (+)-frondosin A.
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
Total synthesis of (+/-)-frondosin B and (+/-)-5-epi-liphagal by using a concise (4+3) cycloaddition approach.
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 novel, facile approach to frondosin B and 5-epi-liphagal via a new [4 + 3]-cycloaddition.
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
Multicomponent coupling approach to (+/-)-frondosin B and a ring-expanded analogue.
[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
Total synthesis and determination of the absolute configuration of frondosin B.
Two concise syntheses of (+/-)-frondosin B (1), an interleukin-8 receptor antagonist, have been achieved from commercially… Expand
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