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The Catalytic Asymmetric Acetalization

2013; Wiley; Volume: 52; Issue: 16 Linguagem: Inglês

10.1002/anie.201300120

1521-3773

Ji Hye Kim, Ilija Čorić, Sreekumar Vellalath, Benjamin List,

Synthetic Organic Chemistry Methods

Angewandte Chemie International EditionVolume 52, Issue 16 p. 4474-4477 Communication The Catalytic Asymmetric Acetalization† Ji Hye Kim, Ji Hye Kim Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, 45470 Mülheim an der Ruhr (Germany)Search for more papers by this authorIlija Čorić, Ilija Čorić Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, 45470 Mülheim an der Ruhr (Germany)Search for more papers by this authorDr. Sreekumar Vellalath, Dr. Sreekumar Vellalath Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, 45470 Mülheim an der Ruhr (Germany)Search for more papers by this authorProf. Dr. Benjamin List, Corresponding Author Prof. Dr. Benjamin List [email protected] Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, 45470 Mülheim an der Ruhr (Germany)Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, 45470 Mülheim an der Ruhr (Germany)===Search for more papers by this author Ji Hye Kim, Ji Hye Kim Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, 45470 Mülheim an der Ruhr (Germany)Search for more papers by this authorIlija Čorić, Ilija Čorić Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, 45470 Mülheim an der Ruhr (Germany)Search for more papers by this authorDr. Sreekumar Vellalath, Dr. Sreekumar Vellalath Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, 45470 Mülheim an der Ruhr (Germany)Search for more papers by this authorProf. Dr. Benjamin List, Corresponding Author Prof. Dr. Benjamin List [email protected] Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, 45470 Mülheim an der Ruhr (Germany)Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, 45470 Mülheim an der Ruhr (Germany)===Search for more papers by this author First published: 19 March 2013 https://doi.org/10.1002/anie.201300120Citations: 127 † We thank H. Schucht for crystal structure analyses. Generous support from the Max Planck Society and the European Research Council (Advanced Grant “High Performance Lewis Acid Organocatalysis, HIPOCAT”) is gratefully acknowledged. Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Graphical Abstract In straitened circumstances: In an asymmetric version of the acid-catalyzed acetalization of aldehydes, a novel member of the chiral confined Brønsted acid family significantly outperformed previously established catalysts, providing cyclic acetals with excellent enantioselectivity (see scheme; Ar=2-iPr-5-MeC6H3). Citing Literature Supporting Information As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Filename Description anie_201300120_sm_miscellaneous_information.pdf3.9 MB miscellaneous_information Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article. Volume52, Issue16April 15, 2013Pages 4474-4477 RelatedInformation