瓊斯氧化反應
瓊斯氧化反應（Jones氧化）是鉻酸在丙酮中將一級和二級醇分別氧化為羧酸和酮的反應。[1][2][3][4][5][6][7]
反應放熱、迅速，產率也較高。該反應中的氧化劑也稱Jones試劑，即三氧化鉻在稀硫酸中的溶液。
反應條件下醛也會被氧化為羧酸。但雙鍵一般不被氧化。
參見[編輯]
- Collins試劑
- 氯鉻酸吡啶鹽（PCC）
- Sarett氧化反應
- 化學反應列表
參考資料[編輯]
- ^ Bowden, K.; Heilbron, I. M.; Jones, E. R. H. 13. Researches on acetylenic compounds. Part I. The preparation of acetylenic ketones by oxidation of acetylenic carbinols and glycols. J. Chem. Soc. 1946: 39. doi:10.1039/jr9460000039.
- ^ Heilbron, I.M.; Jones, E.R.H.; Sondheimer, F. 129. Researches on acetylenic compounds. Part XV. The oxidation of primary acetylenic carbinols and glycols. J. Chem. Soc. 1949: 604. doi:10.1039/jr9490000604.
- ^ Bladon, P. 532. Studies in the sterol group. Part LII. Infra-red absorption of nuclear tri- and tetra-substituted ethylenic centres. J. Chem. Soc. 1951: 2402. doi:10.1039/jr9510002402.
- ^ Jones, E. R. H. 92. The chemistry of the triterpenes. Part XIII. The further characterisation of polyporenic acid A. J. Chem. Soc. 1953: 457. doi:10.1039/jr9530000457.
- ^ Jones, E. R. H. 520. The chemistry of the triterpenes and related compounds. Part XVIII. Elucidation of the structure of polyporenic acid C. J. Chem. Soc. 1953: 2548. doi:10.1039/jr9530002548.
- ^ Jones, E. R. H. 599. The chemistry of the triterpenes and related compounds. Part XIX. Further evidence concerning the structure of polyporenic acid A. J. Chem. Soc. 1953: 3019. doi:10.1039/jr9530003019.
- ^ C. Djerassi, R. Engle and A. Bowers. Notes - The Direct Conversion of Steroidal Δ5-3β-Alcohols to Δ5- and Δ4-3-Ketones. J. Org. Chem. 1956, 21 (12): 1547–1549. doi:10.1021/jo01118a627.
延伸閱讀[編輯]
- Ley, S. V.; Madin, A. (1991). (Review). Comp. Org. Syn. 7: 253–256.
- E. J. Eisenbraun (1973). "Cyclooctanone". Org. Synth.; Coll. Vol. 5: 310.
- J. Meinwald, J. Crandall, and W. E. Hymans (1973). "Nortricyclanone". Org. Synth.; Coll. Vol. 5: 866.