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dactylol

 
National Institutes of Health

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1 relation

Broader (1)

Cycloparaffins

Papers overview

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Review
2019
Review
2019
Bicyclo [6.3.0] Undecane Sesquiterpenoids: Structures, Biological Activities, and Syntheses
Sesquiterpenoids constitute a marvelously varied group of natural products that feature a vast array of molecular architectures… Expand
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2015
2015
Enyne-2-pyrone [4 + 4]-Photocycloaddition: Sesquiterpene Synthesis and a Low-Temperature Cope Rearrangement.
Intramolecular [4 + 4] photoreaction of 2-pyrones with a 1,3-enyne yields an unstable 1,2,5-cyclooctatriene product. Without a C4… Expand
2010
2010
Ring-closing metathesis of allylsilanes as a flexible strategy toward cyclic terpenes. short syntheses of teucladiol, isoteucladiol, poitediol, and dactylol and an attempted synthesis of…
The development of a strategy consisting of allylsilane ring-closing metathesis and subsequent S(E)' electrophilic desilylation… Expand
2010
2010
Synthesis of exo-methylidenecycloalkanes via Allylsilane ring-closing metathesis/SE' electrophilic desilylation. Short syntheses of teucladiol, poitediol, dactylol, and 4beta,6beta-dihydroxy-1alpha…
 
Highly Cited
1999
Highly Cited
1999
Synthesis and Absolute Stereochemical Assignment of (+)-Miyakolide
The first total synthesis of the marine macrolide miyakolide has been achieved, and its absolute stereochemistry has been… Expand
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Highly Cited
1996
Highly Cited
1996
A Concise Total Synthesis of Dactylol via Ring Closing Metathesis.
A straightforward total synthesis of the cyclooctenoid sesquiterpene dactylol (1) and of 3a-epi-dactylol (13) has been achieved… Expand
1986
1986
Total synthesis of the marine sesquiterpenes (±) dactylol and (±)-africanol : a synthetic approach toward (±)-neolemnanyl acetate /
  • W. Ham
  • 1986
    • Corpus ID: 103994713
 
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