Journal article

Stereoselective Total Synthesis of (-)-Spirofungin A by Utilising Hydrogen-Bond Controlled Spiroketalisation

John E Lynch, Shannon D Zanatta, Jonathan M White, Mark A Rizzacasa

Chemistry - A European Journal | WILEY-V C H VERLAG GMBH | Published : 2011

DOI: 10.1002/chem.201002501

Related Projects (1)

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X-Ray Molecular Structure Elucidation Facility (Msef)

X-ray diffraction plays a key role in identification and molecular characterization. X-ray techniques are the single most widely used analyt..

Grants

Awarded by Australian Research Council

Funding Acknowledgements

Financial support for this work was provided by a Australian Research Council: Discovery-Grant (DP0770408).

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Keywords

Spiro Compounds
Streptomyces
Natural-Products
Hydrogen Bonding
Spiroacetal
Crystal-Structure
Physical Sciences
Pyrans
Stereochemistry
Spirofungins
Spiroketals
Chemistry, Multidisciplinary
Science & Technology
Spirofungin-A
Reassignment
Alkyne Group
Selectivity
Natural Products
Molecular Structure
Stereoisomerism
Total Synthesis
Olefin Cross-Metathesis
Hydrogen Bonds
Furans
Chemistry
Monensin Spiroketal