卡羅爾重排反應

卡羅爾重排反應（英語：Carroll rearrangement），又稱卡羅爾-克萊森重排反應，指β-酮酸烯丙酯發生克萊森重排反應產生α-烯丙基-β-酮酸，再經脫羧，得到γ,δ-不飽和酮。^[1]

反應機理

反應最初是用鹼催化，採用一鍋反應，即酯交換（製取β-酮酯）-卡羅爾重排串聯進行，需要苛刻條件（乙酸鈉，170－240℃）。其機理為烯醇發生的克萊森重排然後脫羧（下圖A途徑）。現多採用分步方法進行，主要改進包括雙負離子法（用二異丙基氨基鋰生成雙負離子，然後在室溫或回流下重排，由此得到的酮酸較易分離）^[2]^[3]以及負載在氯化鋁上無溶劑條件下的反應^[4]。

1980年辻二郎對此反應作了改進，他用鈀(0)作催化劑，經過生成中間體烯丙基正離子／羧酸根負離子有機金屬配合物，然後脫羧和烯丙基化，實現了溫和條件下的卡羅爾重排（下圖B途徑）。^[5]

卡羅爾重排的機理

下面用四(三苯基膦)鈀(0)催化的實驗證實了脫羧一步是在烯丙化前發生。^[6]

脫羧烯丙基化

不對稱脫羧烯丙化反應

使用手性配體的不對稱卡羅爾重排也有發展。^[7] 首個不對稱重排由 Burger 等在 2004 年報道，是以三(二亞苄基丙酮)二鈀(0)和Trost配體催化：^[6]

烯醇負離子的不對稱烯丙化

桑野良一等報道了萘酚存在下的卡羅爾重排，反應ee可達88%，但缺點是底物必須要含乙醯氨基基團。^[8]

桑野良一的不對稱卡羅爾重排

又如如下對映歸一性合成：^[9]

莫爾的不對稱卡羅爾重排

不對稱卡羅爾重排也可拓展至烯醇的碳酸酯發生的α-烯丙基化。^[10]

2005年特羅斯特的脫羧烯丙化

參見

參考資料

^ Carroll, M. F. 131. Addition of α,β-unsaturated alcohols to the active methylene group. Part I. The action of ethyl acetoacetate on linalool and geraniol. J. Chem. Soc. 1940: 704–706. doi:10.1039/JR9400000704.
^ J. F. Genus, D. D. Peters, J-F. Ding, T. A. Bryson. The Dianion Carroll Rearrangement - A Cyclic Application. Synlett. 1994: 209–210. doi:10.1055/s-1994-22797.
^ Stephen R. Wilson, Martyn F. Price. The ester enolate Carroll rearrangement. J. Org. Chem. 1984, 49 (4): 722–725. doi:10.1021/jo00178a036.
^ S. I. Pogrebnoi, Y. B. Kalyan, M. Z. Krimer, W. A. Smit. Carrol rearrangement on the surface of chromatographic grade alumina. Tetrahedron Lett. 1987, 28 (41): 4893–4896. doi:10.1016/S0040-4039(00)96654-1.
^ Isao Shimizu, Toshiro Yamada and Jiro Tsuji. Palladium-catalyzed rearrangement of allylic esters of acetoacetic acid to give γ,δ-unsaturated methyl ketones. Tetrahedron Letters. 1980, 21 (33): 3199–3202. doi:10.1016/S0040-4039(00)77444-2.
^ ^6.0 ^6.1 Erin C. Burger and Jon A. Tunge. Asymmetric Allylic Alkylation of Ketone Enolates: An Asymmetric Claisen Surrogate. Org. Lett. 2004, 6 (22): 4113–4115. doi:10.1021/ol048149t.
^ Shu-Li You and Li-Xin Dai. Enantioselective Palladium-Catalyzed Decarboxylative Allylic Alkylations. Angew. Chem. Int. Ed. 2006, 45 (32): 5246–5248. doi:10.1002/anie.200601889.
^ Kuwano, R.; Ishida N.; Murakami, M. Asymmetric Carroll rearrangement of allyl α-acetamido-β-ketocarboxylates catalysed by a chiral palladium complex. Chem. Commun. 2005, (31): 3951–3952. doi:10.1039/b505105c. .
^ Justin T. Mohr, Douglas C. Behenna, Andrew M. Harned, and Brian M. Stoltz. Deracemization of Quaternary Stereocenters by Pd-Catalyzed Enantioconvergent Decarboxylative Allylation of Racemic β-Ketoesters. Angew. Chem. Int. Ed. 2005, 44 (42): 6924–6927. doi:10.1002/anie.200502018.
^ Barry M. Trost and Jiayi Xu. Palladium-Catalyzed Asymmetric Allylic α-Alkylation of Acyclic Ketones. J. Am. Chem. Soc. 2005, 127 (49): 17180–17181. doi:10.1021/ja055968f.

[1] Carroll, M. F. 131. Addition of α,β-unsaturated alcohols to the active methylene group. Part I. The action of ethyl acetoacetate on linalool and geraniol. J. Chem. Soc. 1940: 704–706. doi:10.1039/JR9400000704.

[2] J. F. Genus, D. D. Peters, J-F. Ding, T. A. Bryson. The Dianion Carroll Rearrangement - A Cyclic Application. Synlett. 1994: 209–210. doi:10.1055/s-1994-22797.

[3] Stephen R. Wilson, Martyn F. Price. The ester enolate Carroll rearrangement. J. Org. Chem. 1984, 49 (4): 722–725. doi:10.1021/jo00178a036.

[4] S. I. Pogrebnoi, Y. B. Kalyan, M. Z. Krimer, W. A. Smit. Carrol rearrangement on the surface of chromatographic grade alumina. Tetrahedron Lett. 1987, 28 (41): 4893–4896. doi:10.1016/S0040-4039(00)96654-1.

[5] Isao Shimizu, Toshiro Yamada and Jiro Tsuji. Palladium-catalyzed rearrangement of allylic esters of acetoacetic acid to give γ,δ-unsaturated methyl ketones. Tetrahedron Letters. 1980, 21 (33): 3199–3202. doi:10.1016/S0040-4039(00)77444-2.

[Burger-6] 6.0 ^6.1 Erin C. Burger and Jon A. Tunge. Asymmetric Allylic Alkylation of Ketone Enolates: An Asymmetric Claisen Surrogate. Org. Lett. 2004, 6 (22): 4113–4115. doi:10.1021/ol048149t.

[7] Shu-Li You and Li-Xin Dai. Enantioselective Palladium-Catalyzed Decarboxylative Allylic Alkylations. Angew. Chem. Int. Ed. 2006, 45 (32): 5246–5248. doi:10.1002/anie.200601889.

[8] Kuwano, R.; Ishida N.; Murakami, M. Asymmetric Carroll rearrangement of allyl α-acetamido-β-ketocarboxylates catalysed by a chiral palladium complex. Chem. Commun. 2005, (31): 3951–3952. doi:10.1039/b505105c. .

[9] Justin T. Mohr, Douglas C. Behenna, Andrew M. Harned, and Brian M. Stoltz. Deracemization of Quaternary Stereocenters by Pd-Catalyzed Enantioconvergent Decarboxylative Allylation of Racemic β-Ketoesters. Angew. Chem. Int. Ed. 2005, 44 (42): 6924–6927. doi:10.1002/anie.200502018.

[10] Barry M. Trost and Jiayi Xu. Palladium-Catalyzed Asymmetric Allylic α-Alkylation of Acyclic Ketones. J. Am. Chem. Soc. 2005, 127 (49): 17180–17181. doi:10.1021/ja055968f.

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