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Nishimura, Takahiro, Katoh, Taisuke, Hayashi, Tamio (2007) Rhodium-Catalyzed Aryl Transfer from Trisubstituted Aryl Methanols to α,β-Unsaturated Carbonyl Compounds. Angewandte Chemie International Edition, 46 (26). 4937-4939 doi:10.1002/anie.200700902

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Reference TypeJournal (article/letter/editorial)
TitleRhodium-Catalyzed Aryl Transfer from Trisubstituted Aryl Methanols to α,β-Unsaturated Carbonyl Compounds
JournalAngewandte Chemie International Edition
AuthorsNishimura, TakahiroAuthor
Katoh, TaisukeAuthor
Hayashi, TamioAuthor
Year2007 (June 25)Volume46
Issue26
PublisherWiley
DOIdoi:10.1002/anie.200700902Search in ResearchGate
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Mindat Ref. ID8581105Long-form Identifiermindat:1:5:8581105:4
GUID0
Full ReferenceNishimura, Takahiro, Katoh, Taisuke, Hayashi, Tamio (2007) Rhodium-Catalyzed Aryl Transfer from Trisubstituted Aryl Methanols to α,β-Unsaturated Carbonyl Compounds. Angewandte Chemie International Edition, 46 (26). 4937-4939 doi:10.1002/anie.200700902
Plain TextNishimura, Takahiro, Katoh, Taisuke, Hayashi, Tamio (2007) Rhodium-Catalyzed Aryl Transfer from Trisubstituted Aryl Methanols to α,β-Unsaturated Carbonyl Compounds. Angewandte Chemie International Edition, 46 (26). 4937-4939 doi:10.1002/anie.200700902
In(2007, June) Angewandte Chemie International Edition Vol. 46 (26) Wiley

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Nishimura, Takahiro, Katoh, Taisuke, Hayashi, Tamio (2007) Rhodium-Catalyzed Aryl Transfer from Trisubstituted Aryl Methanols to α,β-Unsaturated Carbonyl Compounds. Angewandte Chemie, 119 (26). 5025-5027 doi:10.1002/ange.200700902
Shintani, Ryo, Takatsu, Keishi, Katoh, Taisuke, Nishimura, Takahiro, Hayashi, Tamio (2008) Rhodium-Catalyzed Rearrangement of Aryl Bis(alkynyl) Carbinols to 3-Alkynyl-1-indanones. Angewandte Chemie International Edition, 47 (8). 1447-1449 doi:10.1002/anie.200704818
Nishimura, Takahiro, Yasuhara, Yuichi, Hayashi, Tamio (2006) Highly Selective 1,6-Addition of Aryl Boronic Acids to α,β,γ,δ-Unsaturated Carbonyl Compounds Catalyzed by an Iridium Complex. Angewandte Chemie International Edition, 45 (31). 5164-5166 doi:10.1002/anie.200601719
Shintani, Ryo, Takatsu, Keishi, Katoh, Taisuke, Nishimura, Takahiro, Hayashi, Tamio (2008) Rhodium-Catalyzed Rearrangement of Aryl Bis(alkynyl) Carbinols to 3-Alkynyl-1-indanones. Angewandte Chemie, 120 (8). 1469-1471 doi:10.1002/ange.200704818
Nishimura, Takahiro, Yasuhara, Yuichi, Hayashi, Tamio (2006) Highly Selective 1,6-Addition of Aryl Boronic Acids to α,β,γ,δ-Unsaturated Carbonyl Compounds Catalyzed by an Iridium Complex. Angewandte Chemie, 118 (31). 5288-5290 doi:10.1002/ange.200601719
Shintani, Ryo, Takeda, Momotaro, Nishimura, Takahiro, Hayashi, Tamio (2010) Chiral Tetrafluorobenzobarrelenes as Effective Ligands for Rhodium-Catalyzed Asymmetric 1,4-Addition of Arylboroxines to β,β-Disubstituted α,β-Unsaturated Ketones. Angewandte Chemie International Edition, 49 (23). 3969-3971 doi:10.1002/anie.201000467
Nishimura, Takahiro, Sawano, Takahiro, Hayashi, Tamio (2009) Asymmetric Synthesis of β-Alkynyl Aldehydes by Rhodium-Catalyzed Conjugate Alkynylation. Angewandte Chemie International Edition, 48 (43). 8057-8059 doi:10.1002/anie.200904486
Dou, Xiaowei, Huang, Yinhua, Hayashi, Tamio (2016) Asymmetric Conjugate Alkynylation of Cyclic α,β-Unsaturated Carbonyl Compounds with a Chiral Diene Rhodium Catalyst. Angewandte Chemie International Edition, 55 (3). 1133-1137 doi:10.1002/anie.201509778
Dou, Xiaowei, Lu, Yixin, Hayashi, Tamio (2016) Base-Free Conditions for Rhodium-Catalyzed Asymmetric Arylation To Produce Stereochemically Labile α-Aryl Ketones. Angewandte Chemie International Edition, 55 (23). 6739-6743 doi:10.1002/anie.201601709
Hayashi, Tamio, Yamamoto, Shohei, Tokunaga, Norihito (2005) Rhodium-Catalyzed Asymmetric 1,6-Addition of Aryl Zinc Reagents to Dienones. Angewandte Chemie International Edition, 44 (27). 4224-4227 doi:10.1002/anie.200500678
Shintani, Ryo, Inoue, Mitsunori, Hayashi, Tamio (2006) Rhodium-Catalyzed Asymmetric Addition of Aryl- and Alkenylboronic Acids to Isatins. Angewandte Chemie International Edition, 45 (20). 3353-3356 doi:10.1002/anie.200600392
 
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