Type
ArticleKAUST Grant Number
KUS-11-006-02Date
2011Permanent link to this record
http://hdl.handle.net/10754/597388
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The tetracyclic core of the integrastatin natural products has been prepared in a convergent and rapid manner. Our strategy relies upon a palladium(ii)-catalyzed oxidative cyclization to form the central [3.3.1]-dioxabicycle of the natural product core. Overall, the core has been completed in only 4 linear steps from known compounds. © 2011 The Royal Society of Chemistry.Citation
Tadross PM, Bugga P, Stoltz BM (2011) A rapid and convergent synthesis of the integrastatin core. Org Biomol Chem 9: 5354. Available: http://dx.doi.org/10.1039/c1ob05725a.Sponsors
This publication is based on work supported by Award No. KUS-11-006-02, made by King Abdullah University of Science and Technology (KAUST). Financial support from Caltech, the Rose Hills Foundation (undergraduate fellowship to P.B.), and the California HIV/AIDS Research Program (graduate fellowship to P.M.T.) is also gratefully acknowledged.Publisher
Royal Society of Chemistry (RSC)Journal
Organic & Biomolecular ChemistryPubMed ID
21681334ae974a485f413a2113503eed53cd6c53
10.1039/c1ob05725a
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