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Evans, P. Andrew, Andrews, William J. (2008) A Sequential Two‐Component Etherification/Oxa‐Conjugate Addition Reaction: Asymmetric Synthesis of (+)‐Leucascandrolide A Macrolactone. Angewandte Chemie International Edition, 47 (29). 5426-5429 doi:10.1002/anie.200801357

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Reference TypeJournal (article/letter/editorial)
TitleA Sequential Two‐Component Etherification/Oxa‐Conjugate Addition Reaction: Asymmetric Synthesis of (+)‐Leucascandrolide A Macrolactone
JournalAngewandte Chemie International Edition
AuthorsEvans, P. AndrewAuthor
Andrews, William J.Author
Year2008 (July 7)Volume47
Issue29
PublisherWiley
DOIdoi:10.1002/anie.200801357Search in ResearchGate
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Mindat Ref. ID8585581Long-form Identifiermindat:1:5:8585581:8
GUID0
Full ReferenceEvans, P. Andrew, Andrews, William J. (2008) A Sequential Two‐Component Etherification/Oxa‐Conjugate Addition Reaction: Asymmetric Synthesis of (+)‐Leucascandrolide A Macrolactone. Angewandte Chemie International Edition, 47 (29). 5426-5429 doi:10.1002/anie.200801357
Plain TextEvans, P. Andrew, Andrews, William J. (2008) A Sequential Two‐Component Etherification/Oxa‐Conjugate Addition Reaction: Asymmetric Synthesis of (+)‐Leucascandrolide A Macrolactone. Angewandte Chemie International Edition, 47 (29). 5426-5429 doi:10.1002/anie.200801357
In(2008, July) Angewandte Chemie International Edition Vol. 47 (29) Wiley

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Evans, P. Andrew, Andrews, William J. (2008) A Sequential Two‐Component Etherification/Oxa‐Conjugate Addition Reaction: Asymmetric Synthesis of (+)‐Leucascandrolide A Macrolactone. Angewandte Chemie, 120 (29). 5506-5509 doi:10.1002/ange.200801357
Evans, P. Andrew, Leahy, David K., Andrews, William J., Uraguchi, Daisuke (2004) Stereodivergent Construction of Cyclic Ethers by a Regioselective and Enantiospecific Rhodium-Catalyzed Allylic Etherification: Total Synthesis of Gaur Acid. Angewandte Chemie International Edition, 43 (36). 4788-4791 doi:10.1002/anie.200460612
Hénon, Hélène, Mauduit, Marc, Alexakis, Alexandre (2008) Regiodivergent 1,4 versus 1,6 Asymmetric Copper-Catalyzed Conjugate Addition. Angewandte Chemie International Edition, 47 (47). 9122-9124 doi:10.1002/anie.200803735
Jung, Hyung Hoon, Seiders, John R., Floreancig, Paul E. (2007) Oxidative Cleavage in the Construction of Complex Molecules: Synthesis of the Leucascandrolide A Macrolactone. Angewandte Chemie International Edition, 46 (44). 8464-8467 doi:10.1002/anie.200702999
Daniels, Blake E., Ni, Jane, Reisman, Sarah E. (2016) Synthesis of Enantioenriched Indolines by a Conjugate Addition/Asymmetric Protonation/Aza-Prins Cascade Reaction. Angewandte Chemie International Edition, 55 (10). 3398-3402 doi:10.1002/anie.201510972
Xiao, Yuanjing, Zhang, Junliang (2008) Tetrasubstituted Furans by a PdII-Catalyzed Three-Component Michael Addition/Cyclization/Cross-Coupling Reaction. Angewandte Chemie International Edition, 47 (10). 1903-1906 doi:10.1002/anie.200704531
Henderson, James A., Phillips, Andrew J. (2008) Total Synthesis of Aburatubolactam A. Angewandte Chemie International Edition, 47 (44). 8499-8501 doi:10.1002/anie.200803593
Kim, Hyoungsu, Park, Yongho, Hong, Jiyong (2009) Stereoselective Synthesis of 2,6-cis-Tetrahydropyrans through a Tandem Allylic Oxidation/Oxa-Michael Reaction Promoted by thegem-Disubstituent Effect: Synthesis of (+)-Neopeltolide Macrolactone. Angewandte Chemie International Edition, 48 (41). 7577-7581 doi:10.1002/anie.200903690
Cheng, Xu, Goddard, Richard, Buth, Gernot, List, Benjamin (2008) Direct Catalytic Asymmetric Three-Component Kabachnik-Fields Reaction. Angewandte Chemie International Edition, 47 (27). 5079-5081 doi:10.1002/anie.200801173
Evans, P. Andrew, Grisin, Aleksandr, Lawler, Michael J. (2012) Diastereoselective Construction of syn-1,3-Dioxanes via a Bismuth-Mediated Two-Component Hemiacetal/Oxa-Conjugate Addition Reaction. Journal Of The American Chemical Society, 134 (6) 2856-2859 doi:10.1021/ja208668u
Sasaki, Keigo, Hayashi, Tamio (2010) Rhodium-Catalyzed Asymmetric Conjugate Addition of Arylboroxines to Borylalkenes: Asymmetric Synthesis of β-Arylalkylboranes. Angewandte Chemie International Edition, 49 (44). 8145-8147 doi:10.1002/anie.201004980
 
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