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Crane, Erika A., Scheidt, Karl A. (2010) Prins-Type Macrocyclizations as an Efficient Ring-Closing Strategy in Natural Product Synthesis. Angewandte Chemie International Edition, 49 (45). 8316-8326 doi:10.1002/anie.201002809

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Reference TypeJournal (article/letter/editorial)
TitlePrins-Type Macrocyclizations as an Efficient Ring-Closing Strategy in Natural Product Synthesis
JournalAngewandte Chemie International Edition
AuthorsCrane, Erika A.Author
Scheidt, Karl A.Author
Year2010 (November 2)Volume49
Issue45
PublisherWiley
DOIdoi:10.1002/anie.201002809Search in ResearchGate
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Mindat Ref. ID8596198Long-form Identifiermindat:1:5:8596198:8
GUID0
Full ReferenceCrane, Erika A., Scheidt, Karl A. (2010) Prins-Type Macrocyclizations as an Efficient Ring-Closing Strategy in Natural Product Synthesis. Angewandte Chemie International Edition, 49 (45). 8316-8326 doi:10.1002/anie.201002809
Plain TextCrane, Erika A., Scheidt, Karl A. (2010) Prins-Type Macrocyclizations as an Efficient Ring-Closing Strategy in Natural Product Synthesis. Angewandte Chemie International Edition, 49 (45). 8316-8326 doi:10.1002/anie.201002809
In(2010, November) Angewandte Chemie International Edition Vol. 49 (45) Wiley

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Crane, Erika A., Scheidt, Karl A. (2010) Die Prins-Makrocyclisierung als effiziente Ringschluss-Strategie in der Naturstoffsynthese. Angewandte Chemie, 122 (45). 8494-8505 doi:10.1002/ange.201002809
Crane, Erika A., Zabawa, Thomas P., Farmer, Rebecca L., Scheidt, Karl A. (2011) Enantioselective Synthesis of (−)-Exiguolide by Iterative Stereoselective Dioxinone-Directed Prins Cyclizations. Angewandte Chemie International Edition, 50 (39). 9112-9115 doi:10.1002/anie.201102790
Crane, Erika A., Gademann, Karl (2016) Capturing Biological Activity in Natural Product Fragments by Chemical Synthesis. Angewandte Chemie International Edition, 55 (12). 3882-3902 doi:10.1002/anie.201505863
Tenenbaum, Jason M., Morris, William J., Custar, Daniel W., Scheidt, Karl A. (2011) Synthesis of (−)-Okilactomycin by a Prins-Type Fragment-Assembly Strategy. Angewandte Chemie International Edition, 50 (26). 5892-5895 doi:10.1002/anie.201102037
Lombardo, Vince M., Thomas, Christopher D., Scheidt, Karl A. (2013) A Tandem Isomerization/Prins Strategy: Iridium(III)/Brønsted Acid Cooperative Catalysis. Angewandte Chemie International Edition, 52 (49). 12910-12914 doi:10.1002/anie.201306462
Crane, Erika A., Zabawa, Thomas P., Farmer, Rebecca L., Scheidt, Karl A. (2011) Enantioselective Synthesis of (−)-Exiguolide by Iterative Stereoselective Dioxinone-Directed Prins Cyclizations. Angewandte Chemie, 123 (39). 9278-9281 doi:10.1002/ange.201102790
Linde, Erika, Olofsson, Berit (2023) Synthesis of Complex Diarylamines through a Ring‐Opening Difunctionalization Strategy**. Angewandte Chemie International Edition, 62 (48) doi:10.1002/anie.202310921
El-azizi, Yassir, Schmitzer, Andreea, Collins, Shawn K. (2006) Exploitation of Perfluorophenyl–Phenyl Interactions for Achieving Difficult Macrocyclizations by Using Ring-Closing Metathesis. Angewandte Chemie International Edition, 45 (6). 968-973 doi:10.1002/anie.200503112
Brichacek, Matthew, Batory, Lindsay A., Njardarson, Jon T. (2010) Stereoselective Ring Expansion of Vinyl Oxiranes: Mechanistic Insights and Natural Product Total Synthesis. Angewandte Chemie International Edition, 49 (9). 1648-1651 doi:10.1002/anie.200906830
Tenenbaum, Jason M., Morris, William J., Custar, Daniel W., Scheidt, Karl A. (2011) Synthesis of (−)-Okilactomycin by a Prins-Type Fragment-Assembly Strategy. Angewandte Chemie, 123 (26). 6014-6017 doi:10.1002/ange.201102037
Hovey, M. Todd, Cohen, Daniel T., Walden, Daniel M., Cheong, Paul H.‐Y., Scheidt, Karl A. (2017) A Carbene Catalysis Strategy for the Synthesis of Protoilludane Natural Products. Angewandte Chemie International Edition, 56 (33). 9864-9867 doi:10.1002/anie.201705308
 
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