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Stereoselective total synthesis of (-)-spirofungin A by utilising hydrogen-bond controlled spiroketalisation.
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Asymmetric total synthesis of (-)-spirofungin A and (+)-spirofungin B.
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Quantum Reality in the Selective Reduction of a Benzofuran System.
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Synthesis of the C-C fragment of the archazolids by complex -homodimer cross metathesis.
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本文引用的文献

1
Total synthesis of apoptolidin A.
Org Lett. 2009 Feb 19;11(4):831-4. doi: 10.1021/ol802829n.
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Synthesis and biological activities of reveromycin A and spirofungin A derivatives.
Bioorg Med Chem Lett. 2008 Jul 1;18(13):3756-60. doi: 10.1016/j.bmcl.2008.05.054. Epub 2008 May 17.
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Spirofungin A: stereoselective synthesis and inhibition of isoleucyl-tRNA synthetase.
Angew Chem Int Ed Engl. 2007;46(46):8854-7. doi: 10.1002/anie.200702440.
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Asymmetric total synthesis of (-)-spirofungin A and (+)-spirofungin B.
Org Lett. 2005 Dec 8;7(25):5573-6. doi: 10.1021/ol052039k.
6
A general model for selectivity in olefin cross metathesis.
J Am Chem Soc. 2003 Sep 17;125(37):11360-70. doi: 10.1021/ja0214882.
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Synthesis of the spirofungin B core by a reductive cyclization strategy.
Org Lett. 2005 Apr 28;7(9):1873-5. doi: 10.1021/ol050589c.
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An affinity probe for isolation of abscisic acid-binding proteins.
J Am Chem Soc. 2005 Feb 16;127(6):1662-4. doi: 10.1021/ja0429059.
10
Short synthesis of the 6,6-spiroketal cores of spirofungins A and B.
Org Lett. 2004 Jul 22;6(15):2587-90. doi: 10.1021/ol0491078.

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