|
[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]
|