羟醛缩合中间体（Aldol condensation）

milarities with compounds already discussed in publications by Wurtz from the same year.

2. Nielsen, A. T.; Houlihan, W. J. Org. React. 1968, 16, 1-438. (Review).

3. Still, W. C.; McDonald, J. H., III. Tetrahedron Lett. 1980, 21, 1031-1034.

4. Mukaiyama, T. Org. React. 1982, 28, 203-331. (Review).

5. Mukaiyama, T.; Kobayashi, S. Org. React. 1994, 46, 1-103. (Review on tin(II) enolates).

6. Johnson, J. S.; Evans, D. A. Acc. Chem. Res. 2000, 33, 325-335. (Review).

7. Denmark, S. E.; Stavenger, R. A. Acc. Chem. Res. 2000, 33, 432-440. (Review).

8. Yang, Z.; He, Y.; Vourloumis, D.; Vallberg, H.; Nicolaou, K. C. Angew. Chem. Int. Ed. 1997, 36, 166-168.

9. Mahrwald, R. (ed.) Modern Aldol Reactions,Wiley-VCH: Weinheim, Germany, 2004. (Book).

12. Doherty, S.; Knight, J. G.; McRae, A.; Harrington, R. W.; Clegg, W. Eur. J. Org. Chem. 2008,1759-1766.

14. Trost, B. M.; Brindle, C. S. Chem. Soc. Rev. 2010, 39, 1600-1632. (Review).

15. Gazaille, J. A.; Abramite, J. A.; Sammakia, T. Org. Lett. 2012, 14, 178-181.

16. Esumi, T.; Yamamoto, C.; Tsugawa, Y.; Toyota, M.; Asakawa, Y.; Fukuyama Y. Org. Lett. 2013, 15, 1898–1901.

撰稿自：

一、Name Reactions （A Collection of Detailed Reaction Mechanisms）, Jie Jack Li, Aldol condensation，page 3-5.

二、Strategic Applications of Named Reactions in OrganicSynthesis, László Kürti and Barbara Czakó, aldol reaction, page 8-9.

三、化学空间：%E5%8A%A0%E6%88%90%E5%8F%8D%E5%BA%94/2014/05/%E4%BA%A4%E5%8F%89%E7%BE%9F%E9%86%9B%E7%BC%A9%E5%90%88%E5%8F%8D%E5%BA%94cross-aldol-reaction.html

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。

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