@article{b99308f1c33a40b0b030e27c12ecdcdc,
title = "The Catalytic Enantioselective Total Synthesis of (+)-Liphagal",
abstract = "Ring a ding: The meroterpenoid natural product (+)-liphagal has been synthesized enantioselectively in 19 steps from commercially available materials. The trans-homodecalin system was achieved by ring expansion followed by stereoselective hydrogenation. Copyright {\textcopyright} 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.",
author = "Day, {Joshua J.} and McFadden, {Ryan M.} and Virgil, {Scott C.} and Helene Kolding and Alleva, {Jennifer L.} 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 the King Abdullah University of Science and Technology (KAUST). We wish to thank the NIH-NIGMS (R01M080269-01), the Gordon and Betty Moore Foundation, Abbott, Amgen, Boehringer Ingelheim, and Caltech for generous funding. R.M.M. thanks Eli Lilly for a graduate fellowship. H.K. acknowledges the travelling scholarship of the Danish Technical University, the Jorcks foundation, and the Otto M{\o}nsteds foundation for financial support. J.L.A. gratefully acknowledges the Amgen Foundation for funding through the Amgen Scholars program. We thank Prof. E. N. Jacobsen and Dr. S. J. Zuend for a kind donation of both (R)-t-leucine and their optimal Strecker catalyst. This publication acknowledges KAUST support, but has no KAUST affiliated authors.",
year = "2011",
month = jun,
day = "10",
doi = "10.1002/anie.201101842",
language = "English (US)",
volume = "50",
pages = "6814--6818",
journal = "Angewandte Chemie International Edition",
issn = "1433-7851",
publisher = "John Wiley and Sons Ltd",
number = "30",
}