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Petrone, David A., Yoon, Hyung, Weinstabl, Harald, Lautens, Mark (2014) Additive Effects in the Palladium-Catalyzed Carboiodination of ChiralN-Allyl Carboxamides. Angewandte Chemie, 126 (30). 8042-8046 doi:10.1002/ange.201404007

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Reference TypeJournal (article/letter/editorial)
TitleAdditive Effects in the Palladium-Catalyzed Carboiodination of ChiralN-Allyl Carboxamides
JournalAngewandte Chemie
AuthorsPetrone, David A.Author
Yoon, HyungAuthor
Weinstabl, HaraldAuthor
Lautens, MarkAuthor
Year2014 (July 21)Volume126
Issue30
PublisherWiley
DOIdoi:10.1002/ange.201404007Search in ResearchGate
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Mindat Ref. ID7325573Long-form Identifiermindat:1:5:7325573:2
GUID0
Full ReferencePetrone, David A., Yoon, Hyung, Weinstabl, Harald, Lautens, Mark (2014) Additive Effects in the Palladium-Catalyzed Carboiodination of ChiralN-Allyl Carboxamides. Angewandte Chemie, 126 (30). 8042-8046 doi:10.1002/ange.201404007
Plain TextPetrone, David A., Yoon, Hyung, Weinstabl, Harald, Lautens, Mark (2014) Additive Effects in the Palladium-Catalyzed Carboiodination of ChiralN-Allyl Carboxamides. Angewandte Chemie, 126 (30). 8042-8046 doi:10.1002/ange.201404007
In(2014, July) Angewandte Chemie Vol. 126 (30) Wiley

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Petrone, David A., Yoon, Hyung, Weinstabl, Harald, Lautens, Mark (2014) Additive Effects in the Palladium-Catalyzed Carboiodination of ChiralN-Allyl Carboxamides. Angewandte Chemie International Edition, 53 (30). 7908-7912 doi:10.1002/anie.201404007
Yoon, Hyung, Petrone, David A., Lautens, Mark (2014) Diastereoselective Palladium-Catalyzed Arylcyanation/Heteroarylcyanation of Enantioenriched N-Allylcarboxamides. Organic Letters, 16. 6420-6423 doi:10.1021/ol503243a
Petrone, David A., Lischka, Matthias, Lautens, Mark (2013) Harnessing Reversible Oxidative Addition: Application of Diiodinated Aromatic Compounds in the Carboiodination Process. Angewandte Chemie, 125 (40). 10829-10832 doi:10.1002/ange.201304923
Jia, Xiaodong, Petrone, David A., Lautens, Mark (2012) A Conjunctive Carboiodination: Indenes by a Double Carbopalladation-Reductive Elimination Domino Process. Angewandte Chemie, 124 (39). 10008-10010 doi:10.1002/ange.201204716
Marchese, Austin D., Lind, Florian, Mahon, Áine E., Yoon, Hyung, Lautens, Mark (2019) Forming Benzylic Iodides via a Nickel Catalyzed Diastereoselective Dearomative Carboiodination Reaction of Indoles. Angewandte Chemie, 131 (15). 5149-5153 doi:10.1002/ange.201900659
Sickert, Marcel, Weinstabl, Harald, Peters, Brendan, Hou, Xiao, Lautens, Mark (2014) Intermolecular Domino Reaction of Two Aryl Iodides Involving Two CH Functionalizations. Angewandte Chemie, 126 (20). 5247-5251 doi:10.1002/ange.201400807
Le, Christine M., Menzies, Perry J. C., Petrone, David A., Lautens, Mark (2015) Synergistic Steric Effects in the Development of a Palladium-Catalyzed Alkyne Carbohalogenation: Stereodivergent Synthesis of Vinyl Halides. Angewandte Chemie, 127 (1). 256-259 doi:10.1002/ange.201409248
Yoon, Hyung, Rölz, Martin, Landau, Felicitas, Lautens, Mark (2017) Palladium-Catalyzed Spirocyclization through C−H Activation and Regioselective Alkyne Insertion. Angewandte Chemie, 129 (36). 11060-11063 doi:10.1002/ange.201706325
Petrone, David A., Lischka, Matthias, Lautens, Mark (2013) Harnessing Reversible Oxidative Addition: Application of Diiodinated Aromatic Compounds in the Carboiodination Process. Angewandte Chemie International Edition, 52 (40). 10635-10638 doi:10.1002/anie.201304923
Weinstabl, Harald, Suhartono, Marcel, Qureshi, Zafar, Lautens, Mark (2013) Total Synthesis of (+)-Linoxepin by Utilizing the Catellani Reaction. Angewandte Chemie, 125 (20). 5413-5416 doi:10.1002/ange.201302327
Jia, Xiaodong, Petrone, David A., Lautens, Mark (2012) A Conjunctive Carboiodination: Indenes by a Double Carbopalladation-Reductive Elimination Domino Process. Angewandte Chemie International Edition, 51 (39). 9870-9872 doi:10.1002/anie.201204716
 
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