[2,3]-Sommelet-Hauser重排的研究进展
Research Progress of [2,3]-Sommelet-Hauser Rearrangement
DOI: 10.12677/JOCR.2021.94011, PDF,    国家科技经费支持
作者: 梁微健*, 周丽江, 樊锁江:浙江师范大学,化学与生命科学学院,浙江 金华;童洪杰:金华市中心医院,重症医学科,浙江 金华
关键词: Sommelet-Hauser重排[2 3]-重排鎓盐Sommelet-Hauser Rearrangement [2 3]-Rearrangement Onium Salt
摘要: Sommelet-Hauser重排(S-H重排)是一类基于鎓盐的[2,3]-重排反应,反应过程中能够形成独特的去芳构化中间体,同时构建新的C-C键。该重排反应于1937年由Sommelet首次发现,随后Hauser等人对该反应过程进行了深入的研究。在Sommelet-Hauser重排反应发现后的很长一段时间里,由于该反应存在较多的副反应通道、产物选择性较差,关于其的进一步研究以及应用的报道较少。近些年来,随着新反应模式的发展以及新催化体系的发现,一系列新的S-H重排反应被相继开发,展现出了优异的选择性和广阔的底物兼容性,所得的反应产物骨架丰富多样。S-H重排反应又逐渐引起科学家的重视。本文通过文献查阅,并进一步分析、归纳,对S-H反应进行了深入地探讨与研究,详细阐述了该类反应的独特机制和反应的发展情况。
Abstract: Sommelet-Hauser rearrangement (S-H rearrangement) is a type of [2,3]-rearrangement reaction based on onium salts. During reaction process of Sommelet-Hauser rearrangement, a unique dearomatization intermediate can be formed and a new C-C bond can be constructed finally. The rearrangement reaction was first discovered by Sommelet in 1937, and then Hauser and coworkers conducted in-depth research to understand the insight of reaction process. Since the S-H rearrangement was first discovered, due to the existence of various side reactions and its poor product selectivity, the progress on this rearrangement reaction is limited. With the development of new reaction modes and the discovery of new catalytic systems in recent years, a series of new S-H rearrangements have been developed one after another, exhibiting excellent selectivity, broad substrate compatibility, and diverse product skeletons. The S-H rearrangement reaction has gradually attracted the attention of scientists. Through literature review and further analysis, the unique mechanism and recent advance of S-H rearrangement were discussed in this paper.
文章引用:梁微健, 周丽江, 童洪杰, 樊锁江. [2,3]-Sommelet-Hauser重排的研究进展[J]. 有机化学研究, 2021, 9(4): 92-107. https://doi.org/10.12677/JOCR.2021.94011

参考文献

[1] Tayama, E. (2015) Recent Advances in the Base-Induced Sommelet-Hauser Rearrangement of Amino Acid Derived Ammonium Ylides. The Chemical Record, 15, 789-800. [Google Scholar] [CrossRef] [PubMed]
[2] Tayama, E. (2016) Ring-Substitution, Enlargement, and Contraction by Base-Induced Rearrangements of n-Heterocyclic Ammonium Salts. Heterocycles, 92, 793-828. [Google Scholar] [CrossRef
[3] Sommelet, M. and Hebd, C.R. (1937) Surunt mode particulier de rearrangement intramo-lcalaur. Comptes Rendus Hebdomadaires des Séances de l Académie des Sciences. D: Sciences Naturelles, 205, 56-58.
[4] Brasen, W.R. and Hauser, C.R. (1954) 2-Methylbenzyldimethylamine. Organic Syntheses, 34, 61-63. [Google Scholar] [CrossRef
[5] Lednicbr, D. and Hauser, C.R. (1957) A Novel Ring Enlargement Involving the Ortho Substitution Rearrangement by Means of Sodium Amide in Liquid Ammonia. Journal of the American Chemical Society, 75, 4449-4451. [Google Scholar] [CrossRef
[6] Nakano, M. and Sato, Y. (1985) A Convenient Synthesis of o-Methylbenzylamine Derivatives from Benzyl Halides: The Improved Sommelet-Hauser Rearrangement. Chemical Communications, No. 23, 1684-1685. [Google Scholar] [CrossRef
[7] Narita, K., Shirai, N. and Sato, Y. (1997) Rearrangement of 2-Benzocycloammonium N-Methylides. The Journal of Organic Chemistry, 62, 2544-2549. [Google Scholar] [CrossRef] [PubMed]
[8] Maeda, Y. and Sato, Y. (1996) Reaction of N,N-Dimethyl-N-[(trialkylstannyl)methyl]benzylammonium Iodides with Organolithium Compounds. The Journal of Organic Chemistry, 61, 5188-5190. [Google Scholar] [CrossRef
[9] Maeda, Y., Shirai, N. and Sato, Y. (1994) Chemical Behaviour of Trimethylammonium N-methylides Substituted with Nitrogen-Containing Heteroaromatic Rings. Rearrangement of N,N-dimethyl(pyridylmethyl)ammonium, N,N-dimethyl-(1- methylpyrrolylmethyl)ammonium and N,N-dimethyl-(1-methylindolylmethyl)ammonium N-methylides. Journal of the Chemical Society, Perkin Transactions, 1, 393-398. [Google Scholar] [CrossRef
[10] Jonczyk, A. and Lipiak, D. (1991) Reaction of Organic Anions. 166. Sigmatropic Rearrangements of Ammonium Benzylides: New Preparative and Mechanistic Aspects. The Journal of Organic Chemistry, 56, 6933-6937. [Google Scholar] [CrossRef
[11] Eiji, T., Keisuke, T., Hajime, I. and Eietsu, H. (2010) Remarkable Enhancement Effect of Potassium Tert-Butoxide/THF Solution in Base-Induced Sommelet-Hauser Rearrangements. Tetrahedron, 66, 9389-9395. [Google Scholar] [CrossRef
[12] Kimura, H., et al. (2016) Ring-Strain Effects in Base-Induced Sommelet-Hauser Rearrangement: Application to Successive Stereocontrolled Transformations. European Journal of Organic Chemistry, 21, 3631-3641. [Google Scholar] [CrossRef
[13] Eiji, T., Shintaro, N. and Takeshi, N. (2006) Asymmetric [1,2] Stevens Rearrangement of (S)-N-BenzylicProline-Derived Ammonium Salts under Biphasic Conditions. Chemistry Letters, 35, 478-479. [Google Scholar] [CrossRef
[14] Tayama, E. and Kimura, H. (2007) Asymmetric Sommelet-Hauser Rearrangement of N-benzylic Ammonium Salts. Angewandte Chemie International Edition, 46, 8869-8887. [Google Scholar] [CrossRef] [PubMed]
[15] Biju, A.T., et al. (2019) The Aryne Sommelet-Hauser Rearrangement. Chemical Communications, 55, 3004-3007. [Google Scholar] [CrossRef
[16] Gu, Z.H., Pan, C.Q., et al. (2018) Unusual Biaryl Torsional Strain Promotes Reactivity in Cu-Catalyzed Sommelet-Hauser Rearrangement. Chemical Science, 9, 5850-5854. [Google Scholar] [CrossRef
[17] Ikeda, M., Kazutoshi, I., et al. (1991) Synthesis of Ortho-Substituted Arylacetic Ester and Related Compounds by Means of Sommelet-Hauser Rearrangement of Sulfur Ylides. Chemical and Pharmaceutical Bulletin, 39, 2878-2882. [Google Scholar] [CrossRef
[18] Yamamoto, M., Kakinuma, M., et al. (1989) Sommelet-Hauser Rearrangement of Oxygen and Sulfur Containing Heteomatic Sulfonium Ylide. The Chemical Society of Japan, 3, 958-960. [Google Scholar] [CrossRef
[19] Aggarwal, V.K., Smith, H.W., et al. (2000) Catalytic Cyclopropanation of Electron Deficient Alkenes Mediated by Chiral and Achiral Sulfides: Scope and Limitations in Reactions Involving Phenyldiazomethane and Ethyl Diazoacetate. Journal of the Chemical Society, Perkin Transactions, 1, 3267-3276. [Google Scholar] [CrossRef
[20] Wang, J.B., Liao, M.Y., et al. (2008) Rh(II)-Catalyzed Sommelet-Hauser Rearrangement. Organic Letters, 5, 693-696. [Google Scholar] [CrossRef] [PubMed]
[21] Koenigs, R.M. and Jana, S. (2019) Rhodium-Catalyzed Carbene Transfer Reactions for Sigmatropic Rearrangement Reactions of Selenium Ylides. Organic Letters, 21, 3653-3657. [Google Scholar] [CrossRef] [PubMed]
[22] Sripati, J., Rene, M. and Koenigs, Y.Z., (2019) Rhodium-Catalyzed Carbene Transfer Reactions for Sigmatropic Rearrangement Reactions of Selenium Ylides. Organic Letters, 21, 3653-3657. [Google Scholar] [CrossRef] [PubMed]
[23] Jurberg, I. and Davies, H.M.L. (2018) Blue Light-Promoted Photolysis of Aryldiazoacetates. Chemical Science, 9, 5112-5118. [Google Scholar] [CrossRef
[24] Sheng, Z., Zhang, Z., Chu, C., Zhang, Y. and Wang, J. (2017) Transition Metal-Catalyzed [2,3]-sigmatropic Rearrangements of Ylides: An Update of the Most Recent Advances. Tetrahedron, 73, 4011-4022. [Google Scholar] [CrossRef
[25] Sweeney, J.B. (2009) Sigmatropic Rearrangements of “Onium” Ylids. Chemical Society Reviews, 38, 1027-1038. [Google Scholar] [CrossRef] [PubMed]
[26] Rene, M. and Koenigs, Y.Z. (2019) Photochemical, Metal-Free Sigmatropic Rearrangement Reactions of Sulfur Ylides. Chemistry—A European Journal, 27, 6703-6706. [Google Scholar] [CrossRef] [PubMed]
[27] Feng, X.M., Lin, X.B., et al. (2019) Asymmetric Catalytic [2,3]-Stevens and Sommelet-Hauser Rearrangements of -Diazopyrazoleamides with Sulfides. Angewandte Chemie International Edition, 58, 13492-13498. [Google Scholar] [CrossRef] [PubMed]
[28] Wang, J.B. and Li, S.S. (1972) Cu(I)/Chiral Bisoxazoline-Catalyzed Enantioselective Sommelet-Hauser Rearrangement of Sulfoniumylides. Journal of the American Chemical Society, 8, 2718-2719.
[29] Gassman, P.G. and Bergen, J.V. (1998) A General Method for the Synthesis of Oxindoles. Tetrahedron Letters, 39, 6207-6210.
[30] Liao, M.Y., et al. (2008) Rh(II)-Catalyzed Sommelet-Hauser Rearrangement. Organic Letters, 10, 693-696. [Google Scholar] [CrossRef] [PubMed]
[31] Wang, J.B. and Li, Y.Y. (2011) Catalytic Thia-Sommelet-Hauser Rearrangement: Application to the Synthesis of Oxindoles. Organic Letters, 5, 1210-1213. [Google Scholar] [CrossRef] [PubMed]
[32] Pfitzner, K.E., et al. (1965) The Reactions of Phenols with Oxysulfoniumcations. Journal of the American Chemical Society, 87, 4658-4659. [Google Scholar] [CrossRef
[33] Burden, M.G. and Moffatt, J.G. (1967) Sulfoxide-Carbodiimide Reactions. V. Reactions of 2,6-Disubstituted Phenols. Journal of the American Chemical Society, 89, 4725-4735. [Google Scholar] [CrossRef