@article{edcd8d5029d141f49150f21f7c0564b4,
title = "A rapid and convergent synthesis of the integrastatin core",
abstract = "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. {\textcopyright} 2011 The Royal Society of Chemistry.",
author = "Tadross, {Pamela M.} and Pradeep Bugga and Stoltz, {Brian M.}",
note = "KAUST Repository Item: Exported on 2020-10-01 Acknowledged KAUST grant number(s): KUS-11-006-02 Acknowledgements: 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. This publication acknowledges KAUST support, but has no KAUST affiliated authors.",
year = "2011",
doi = "10.1039/c1ob05725a",
language = "English (US)",
volume = "9",
pages = "5354",
journal = "Organic & Biomolecular Chemistry",
issn = "1477-0520",
publisher = "Royal Society of Chemistry",
number = "15",
}