We gratefully thank Prof. Hiroshi Nakazawa and Dr. Masumi Itazaki at Osaka City University for measurements of elemental analyses and Prof. Tamotsu Takahashi at Hokkaido University for generous donation of zirconocene dichloride. This work was supported by a Grant-in-Aid for Scientific Research on Priority Areas “Advanced Molecular Transformations of Carbon Resources” from the Ministry of Education, Culture, Sports, Science and Technology (Japan).
Communication
Highly Regio- and Stereoselective Synthesis of Multialkylated Olefins through Carbozirconation of Alkynylboronates and Sequential Negishi and Suzuki–Miyaura Coupling Reactions†
Article first published online: 9 AUG 2011
DOI: 10.1002/anie.201103601
Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Issue

Angewandte Chemie International Edition
Volume 50, Issue 37, pages 8660–8664, September 5, 2011
Additional Information
How to Cite
Nishihara, Y., Okada, Y., Jiao, J., Suetsugu, M., Lan, M.-T., Kinoshita, M., Iwasaki, M. and Takagi, K. (2011), Highly Regio- and Stereoselective Synthesis of Multialkylated Olefins through Carbozirconation of Alkynylboronates and Sequential Negishi and Suzuki–Miyaura Coupling Reactions. Angew. Chem. Int. Ed., 50: 8660–8664. doi: 10.1002/anie.201103601
- †
Publication History
- Issue published online: 1 SEP 2011
- Article first published online: 9 AUG 2011
- Manuscript Received: 26 MAY 2011
Funded by
- Grant-in-Aid for Scientific Research
- Ministry of Education, Culture, Sports, Science and Technology
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