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Palladium‐Catalyzed Direct Functionalization of 2‐Aminobutanoic Acid Derivatives: Application of a Convenient and Versatile Auxiliary

2013; Wiley; Volume: 125; Issue: 46 Linguagem: Inglês

10.1002/ange.201306583

1521-3757

Mengyang Fan, Dawei Ma,

Synthesis and Catalytic Reactions

Angewandte ChemieVolume 125, Issue 46 p. 12374-12377 Zuschrift Palladium-Catalyzed Direct Functionalization of 2-Aminobutanoic Acid Derivatives: Application of a Convenient and Versatile Auxiliary† Mengyang Fan, Mengyang Fan State Key Laboratory of Bioorganic & Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032 (China)Search for more papers by this authorProf. Dr. Dawei Ma, Corresponding Author Prof. Dr. Dawei Ma madw@mail.sioc.ac.cn State Key Laboratory of Bioorganic & Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032 (China)State Key Laboratory of Bioorganic & Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032 (China)Search for more papers by this author Mengyang Fan, Mengyang Fan State Key Laboratory of Bioorganic & Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032 (China)Search for more papers by this authorProf. Dr. Dawei Ma, Corresponding Author Prof. Dr. Dawei Ma madw@mail.sioc.ac.cn State Key Laboratory of Bioorganic & Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032 (China)State Key Laboratory of Bioorganic & Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032 (China)Search for more papers by this author First published: 23 September 2013 https://doi.org/10.1002/ange.201306583Citations: 45 † We are grateful to the National Basic Research Program of China (973 Program, grant 2010CB833200), Chinese Academy of Sciences, and the National Natural Science Foundation of China (grant 21132008 & 20921091) for financial support. Read the full textAboutPDF ToolsRequest permissionAdd to favorites 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 Share a linkShare onFacebookTwitterLinkedInRedditWechat Graphical Abstract Die gut verfügbare Hilfsgruppe 2-Methoxyiminoacetyl erleichtert palladiumkatalysierte γ-Arylierungen an C(sp3)-H-Bindungen. Das Auxiliar kann durch Behandlung mit 1 n KOH bei Raumtemperatur leicht entfernt werden; alternativ lässt es sich für Peptidsynthesen in eine Glycineinheit umwandeln. 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 ange_201306583_sm_miscellaneous_information.pdf14.4 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. Volume125, Issue46November 11, 2013Pages 12374-12377 This is the German version of Angewandte Chemie. Note for articles published since 1962: Do not cite this version alone. Take me to the International Edition version with citable page numbers, DOI, and citation export. We apologize for the inconvenience. RelatedInformation