期刊
JOURNAL OF ORGANOMETALLIC CHEMISTRY
卷 754, 期 -, 页码 88-93出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jorganchem.2013.12.046
关键词
1,3-Dienes; Metal dienyls; Grignard reactions; Hydrosilylation; Enyne cross metathesis
资金
- National Science Foundation [CHE-0749759]
- NMR
A number of 2-silicon substituted 1,3-dienes have been prepared by one of three routes: 1) Reactions of 1,3-dienyl Grignard reagents with silyl electrophiles or silyl Grignard reagents with 1,3-dienyl electrophiles; 2) Hydrosilylation of enynes; 3) Enyne cross metathesis. The strengths and limitations of each preparative method are discussed. (C) 2013 Elsevier B. V. All rights reserved.
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