Die Nickel-katalysierte Homoallylierung von Aldehyden und Ketonen mit 1,3-Dienen und ihre komplementäre Unterstützung durch Diethylzink und Triethylboran
1999; Wiley; Volume: 111; Issue: 3 Linguagem: Alemão
10.1002/(sici)1521-3757(19990201)111
ISSN1521-3757
AutoresMasanari Kimura, Hidetaka Fujimatsu, Akihiro Ezoe, Kazufumi Shibata, Masamichi Shimizu, Satoru Matsumoto, Yoshinao Tamaru,
Tópico(s)Asymmetric Hydrogenation and Catalysis
ResumoAngewandte ChemieVolume 111, Issue 3 p. 410-413 Zuschrift Die Nickel-katalysierte Homoallylierung von Aldehyden und Ketonen mit 1,3-Dienen und ihre komplementäre Unterstützung durch Diethylzink und Triethylboran Masanari Kimura, Masanari Kimura Department of Applied Chemistry, Faculty of Engineering, Nagasaki University, 1-14 Bunkyo-machi, Nagasaki 852–8521, Japan, Fax: (+81) 958-47-9008Search for more papers by this authorHidetaka Fujimatsu, Hidetaka Fujimatsu Department of Applied Chemistry, Faculty of Engineering, Nagasaki University, 1-14 Bunkyo-machi, Nagasaki 852–8521, Japan, Fax: (+81) 958-47-9008Search for more papers by this authorAkihiro Ezoe, Akihiro Ezoe Department of Applied Chemistry, Faculty of Engineering, Nagasaki University, 1-14 Bunkyo-machi, Nagasaki 852–8521, Japan, Fax: (+81) 958-47-9008Search for more papers by this authorKazufumi Shibata, Kazufumi Shibata Department of Applied Chemistry, Faculty of Engineering, Nagasaki University, 1-14 Bunkyo-machi, Nagasaki 852–8521, Japan, Fax: (+81) 958-47-9008Search for more papers by this authorMasamichi Shimizu, Masamichi Shimizu Department of Applied Chemistry, Faculty of Engineering, Nagasaki University, 1-14 Bunkyo-machi, Nagasaki 852–8521, Japan, Fax: (+81) 958-47-9008Search for more papers by this authorSatoru Matsumoto, Satoru Matsumoto Department of Applied Chemistry, Faculty of Engineering, Nagasaki University, 1-14 Bunkyo-machi, Nagasaki 852–8521, Japan, Fax: (+81) 958-47-9008Search for more papers by this authorYoshinao Tamaru, Yoshinao Tamaru tamaru@net.nagasaki.u-ac.jp Department of Applied Chemistry, Faculty of Engineering, Nagasaki University, 1-14 Bunkyo-machi, Nagasaki 852–8521, Japan, Fax: (+81) 958-47-9008Search for more papers by this author Masanari Kimura, Masanari Kimura Department of Applied Chemistry, Faculty of Engineering, Nagasaki University, 1-14 Bunkyo-machi, Nagasaki 852–8521, Japan, Fax: (+81) 958-47-9008Search for more papers by this authorHidetaka Fujimatsu, Hidetaka Fujimatsu Department of Applied Chemistry, Faculty of Engineering, Nagasaki University, 1-14 Bunkyo-machi, Nagasaki 852–8521, Japan, Fax: (+81) 958-47-9008Search for more papers by this authorAkihiro Ezoe, Akihiro Ezoe Department of Applied Chemistry, Faculty of Engineering, Nagasaki University, 1-14 Bunkyo-machi, Nagasaki 852–8521, Japan, Fax: (+81) 958-47-9008Search for more papers by this authorKazufumi Shibata, Kazufumi Shibata Department of Applied Chemistry, Faculty of Engineering, Nagasaki University, 1-14 Bunkyo-machi, Nagasaki 852–8521, Japan, Fax: (+81) 958-47-9008Search for more papers by this authorMasamichi Shimizu, Masamichi Shimizu Department of Applied Chemistry, Faculty of Engineering, Nagasaki University, 1-14 Bunkyo-machi, Nagasaki 852–8521, Japan, Fax: (+81) 958-47-9008Search for more papers by this authorSatoru Matsumoto, Satoru Matsumoto Department of Applied Chemistry, Faculty of Engineering, Nagasaki University, 1-14 Bunkyo-machi, Nagasaki 852–8521, Japan, Fax: (+81) 958-47-9008Search for more papers by this authorYoshinao Tamaru, Yoshinao Tamaru tamaru@net.nagasaki.u-ac.jp Department of Applied Chemistry, Faculty of Engineering, Nagasaki University, 1-14 Bunkyo-machi, Nagasaki 852–8521, Japan, Fax: (+81) 958-47-9008Search for more papers by this author First published: February 1, 1999 https://doi.org/10.1002/(SICI)1521-3757(19990201)111:3 3.0.CO;2-HCitations: 31AboutPDF 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 Abstract Die regio- und stereoselektive Homoallylierung von gesättigten Aldehyden und Ketonen, die Bishomoallylalkohole 1,3-anti-1 liefert, wird mit [Ni(acac)2] und Et2Zn erreicht [Gl. (a)]. Dieses neue katalytische System ergänzt die zuvor beschriebene Kombination von [Ni(acac)2] und Et3B, die vorteilhaft bei der Homoallylierung ungesättigter und aromatischer Aldehyde ist. acac=acetylacetonato. Citing Literature Volume111, Issue3February 1, 1999Pages 410-413 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
Referência(s)