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Volumn 17, Issue 6, 2012, Pages 7348-7355

Ring-expansion reaction of oximes with aluminum reductants

Author keywords

Aluminum reductant; Cyclopentyl methyl ether (CPME); Dichloroaluminum hydride (AlHCl 2); Rearrangement of oxime; Ring expansion of oxime

Indexed keywords

ALUMINUM DERIVATIVE; OXIME; REDUCING AGENT;

EID: 84862992825     PISSN: None     EISSN: 14203049     Source Type: Journal    
DOI: 10.3390/molecules17067348     Document Type: Article
Times cited : (21)

References (16)
  • 1
    • 0000766506 scopus 로고    scopus 로고
    • Regioselective synthesis of several heterocyclic fused azepines using diisobutylaluminum hydride
    • Cho, H.; Murakami, K.; Nakanishi, H.; Isoshima, H.; Hayakawa, K.; Uchida, I. Regioselective synthesis of several heterocyclic fused azepines using diisobutylaluminum hydride. Heterocycles 1998, 48, 919-927. (Pubitemid 128657507)
    • (1998) Heterocycles , vol.48 , Issue.5 , pp. 919-927
    • Cho, H.1    Murakami, K.2    Nakanishi, H.3    Isoshima, H.4    Hayakawa, K.5    Uchida, I.6
  • 2
    • 67649874785 scopus 로고    scopus 로고
    • Regiospecific synthesis of unsubstituted basic skeletons of heterocycles containing nitrogen neighboring an aromatic ring by the reductive ring expansion reaction using diisobutylaluminum hydride
    • Cho, H.; Iwama, Y.; Sugimoto, K.; Kwon, E.; Tokuyama, H. Regiospecific synthesis of unsubstituted basic skeletons of heterocycles containing nitrogen neighboring an aromatic ring by the reductive ring expansion reaction using diisobutylaluminum hydride. Heterocycles 2009, 78, 1183-1190.
    • (2009) Heterocycles , vol.78 , pp. 1183-1190
    • Cho, H.1    Iwama, Y.2    Sugimoto, K.3    Kwon, E.4    Tokuyama, H.5
  • 3
    • 75749128224 scopus 로고    scopus 로고
    • Regioselective synthesis of heterocycles containing nitrogen neighboring an aromatic ring by reductive ring expansion using diisobutylaluminum hydride (DIBALH) and studies on the reaction mechanism
    • Cho, H.; Iwama, Y.; Sugimoto, K.; Mori, S.; Tokuyama, H. Regioselective synthesis of heterocycles containing nitrogen neighboring an aromatic ring by reductive ring expansion using diisobutylaluminum hydride (DIBALH) and studies on the reaction mechanism. J. Org. Chem. 2010, 75, 627-636.
    • (2010) J. Org. Chem. , vol.75 , pp. 627-636
    • Cho, H.1    Iwama, Y.2    Sugimoto, K.3    Mori, S.4    Tokuyama, H.5
  • 4
    • 0000614533 scopus 로고
    • Diisobutylaluminum hydride. A novel reagent for the reduction of oximes
    • Sasatani, S.; Miyazaki, T.; Maruoka, K.; Yamamoto, H. Diisobutylaluminum hydride. A novel reagent for the reduction of oximes. Tetrahedron Lett. 1983, 24, 4711-4712.
    • (1983) Tetrahedron Lett. , vol.24 , pp. 4711-4712
    • Sasatani, S.1    Miyazaki, T.2    Maruoka, K.3    Yamamoto, H.4
  • 6
    • 79952775359 scopus 로고    scopus 로고
    • Regiospecific rearrangement of hydroxylamines to secondary amines using diisobutylaluminum hydride
    • Cho, H.; Sugimoto, K.; Iwama, Y.; Mitsuhashi, N.; Okano, K.; Tokuyama, H. Regiospecific rearrangement of hydroxylamines to secondary amines using diisobutylaluminum hydride. Heterocycles 2011, 82, 1633-1644.
    • (2011) Heterocycles , vol.82 , pp. 1633-1644
    • Cho, H.1    Sugimoto, K.2    Iwama, Y.3    Mitsuhashi, N.4    Okano, K.5    Tokuyama, H.6
  • 9
    • 33947332955 scopus 로고
    • Selective Reductions. X. Reaction of aluminum hydride with selected organic compounds containing representative functional groups. Comparison of the reducing characteristics of lithium aluminum hydride and its derivatives
    • Brown, H. C.; Yoon, N. M. Selective Reductions. X. Reaction of aluminum hydride with selected organic compounds containing representative functional groups. comparison of the reducing characteristics of lithium aluminum hydride and its derivatives. J. Am. Chem. Soc. 1966, 88, 1464-1472.
    • (1966) J. Am. Chem. Soc. , vol.88 , pp. 1464-1472
    • Brown, H.C.1    Yoon, N.M.2
  • 10
    • 33947334344 scopus 로고
    • The composition of "mixed hydride" reagents. A study of the Schlesinger reaction
    • Ashby, E. C.; Prather, J. The composition of "mixed hydride" reagents. A study of the Schlesinger reaction. J. Am. Chem. Soc. 1966, 88, 729-733.
    • (1966) J. Am. Chem. Soc. , vol.88 , pp. 729-733
    • Ashby, E.C.1    Prather, J.2
  • 11
    • 33947302910 scopus 로고
    • The mechanism of mixed hydride reductions. Effects of reagent composition, nature of halogen, and solvating ligand on the mechanism of epoxide reduction
    • Ashby, E. C.; Cooke, B. The mechanism of mixed hydride reductions. Effects of reagent composition, nature of halogen, and solvating ligand on the mechanism of epoxide reduction. J. Am. Chem. Soc. 1968, 90, 1625-1630.
    • (1968) J. Am. Chem. Soc. , vol.90 , pp. 1625-1630
    • Ashby, E.C.1    Cooke, B.2
  • 12
    • 84862986103 scopus 로고
    • Reduction of oximes with sodium bis (2-methoxyethoxy) - Aluminum hydride
    • Orlova, E. K.; Kucherova, N. F. Reduction of oximes with sodium bis (2-methoxyethoxy) - aluminum hydride. Khim. Geterotsikl. Soed. 1980, 6, 853.
    • (1980) Khim. Geterotsikl. Soed. , vol.6 , pp. 853
    • Orlova, E.K.1    Kucherova, N.F.2
  • 13
    • 37049004764 scopus 로고
    • Synthesis of 2, 3, 4, 5-tetrahydro-1, 5-benzox (and thi) azepines and their utilization for the preparation of condensed indoles
    • Orlova, E. K.; Sharkova, N. M.; Meshcheryakova, L. M.; Zagorevskii, V. A.; Kucherova, N. F. Synthesis of 2, 3, 4, 5-tetrahydro-1, 5-benzox (and thi) azepines and their utilization for the preparation of condensed indoles. Khim. Geterotsikl. Soed. 1975, 9, 1262-1266.
    • (1975) Khim. Geterotsikl. Soed. , vol.9 , pp. 1262-1266
    • Orlova, E.K.1    Sharkova, N.M.2    Meshcheryakova, L.M.3    Zagorevskii, V.A.4    Kucherova, N.F.5
  • 15
    • 34247266658 scopus 로고    scopus 로고
    • Cyclopentyl methyl ether as a new and alternative process solvent
    • Watanabe, K.; Yamagiwa, N.; Torisawa, Y. Cyclopentyl methyl ether as a new and alternative process solvent. Org. Process Res. Dev. 2007, 11, 251-258.
    • (2007) Org. Process Res. Dev. , vol.11 , pp. 251-258
    • Watanabe, K.1    Yamagiwa, N.2    Torisawa, Y.3
  • 16
    • 67650022809 scopus 로고    scopus 로고
    • Improved Pinner reaction with CPME as a solvent
    • Watanabe, K.; Kogoshi, N.; Miki, H.; Torisawa, Y. Improved Pinner reaction with CPME as a solvent. Synth. Comm. 2009, 39, 2008-2013.
    • (2009) Synth. Comm. , vol.39 , pp. 2008-2013
    • Watanabe, K.1    Kogoshi, N.2    Miki, H.3    Torisawa, Y.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.