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格氏反应

维基百科,自由的百科全书
(重定向自格林尼亚反应

格氏反应是一种有机金属化学反应,该反应需在无水条件下将碳烷基烯丙基乙烯基芳基卤化镁(格氏试剂加成羰基[1][2]。此反应对碳-碳键的形成具有重要意义[3][4]

參考文獻

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  1. ^ Smith, Michael B.; March, Jerry, Advanced Organic Chemistry: Reactions, Mechanisms, and Structure 6th, New York: Wiley-Interscience, 2007, ISBN 978-0-471-72091-1 
  2. ^ Ouellette, Robert J.; Rawn, J. David, Ouellette, Robert J.; Rawn, J. David , 编, 15 - Alcohols: Reactions and Synthesis, Organic Chemistry (Boston: Elsevier), 2014-01-01: 491–534 [2023-11-06], ISBN 978-0-12-800780-8, doi:10.1016/b978-0-12-800780-8.00015-2 
  3. ^ Shirley, D. A. The Synthesis of Ketones from Acid Halides and Organometallic Compounds of Magnesium, Zinc, and Cadmium. Org. React. 1954, 8: 28–58. 
  4. ^ Huryn, D. M. Carbanions of Alkali and Alkaline Earth Cations: (ii) Selectivity of Carbonyl Addition Reactions. Trost, B. M.; Fleming, I. (编). Comprehensive Organic Synthesis, Volume 1: Additions to C—X π-Bonds, Part 1. Elsevier Science. 1991: 49–75. ISBN 978-0-08-052349-1. doi:10.1016/B978-0-08-052349-1.00002-0.