-
1
-
-
0000766506
-
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
-
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
-
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
-
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
-
5
-
-
9144262488
-
Synthesis and Structure-Activity Relationships of 5,6,7,8-Tetrahydro-4H- thieno[3,2-b]azepine Derivatives: Novel Arginine Vasopressin Antagonists
-
DOI 10.1021/jm030287l
-
Cho, H.; Murakami, K.; Nakanishi, H.; Fujisawa, A.; Isoshima, H.; Niwa, M.; Hayakawa, K.; Hase, Y.; Uchida, I.; Watanabe, H.; et al. Synthesis and structure-activity relationships of 5, 6, 7, 8-tetrahydro-4H-thieno[3, 2-b]azepine derivatives: Novel arginine vasopressin antagonists. J. Med. Chem. 2004, 47, 101-109 (Pubitemid 38040494)
-
(2004)
Journal of Medicinal Chemistry
, vol.47
, Issue.1
, pp. 101-109
-
-
Cho, H.1
Murakami, K.2
Nakanishi, H.3
Fujisawa, A.4
Isoshima, H.5
Niwa, M.6
Hayakawa, K.7
Hase, Y.8
Uchida, I.9
Watanabe, H.10
Wakitani, K.11
Aisaka, K.12
-
6
-
-
79952775359
-
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
-
7
-
-
28044468867
-
Facile rearrangement of O-silylated oximes on reduction with boron trifluoride/borane
-
DOI 10.1021/jo0516178
-
Ortiz-Marciales, M.; Rivera, L. D.; Jesús, M. D.; Espinosa, S.; Benjamin, J. A.; Casanova, O. E.; Figueroa, I. G.; Rodriguez, S.; Correa, W. Facile rearrangement of O-Silylated Oximes on reduction with boron trifluoride/borane. J. Org. Chem. 2005, 70, 10132-10134. (Pubitemid 41689186)
-
(2005)
Journal of Organic Chemistry
, vol.70
, Issue.24
, pp. 10132-10134
-
-
Ortiz-Marciales, M.1
Rivera, L.D.2
De Jesus, M.3
Espinosa, S.4
Benjamin, J.A.5
Casanova, O.E.6
Figueroa, I.G.7
Rodriguez, S.8
Correa, W.9
-
8
-
-
0008158084
-
The lithium aluminum hydride-aluminum chloride reduction of oximes
-
Rerick, M. N.; Trottier, C. H.; Daignault, R. A.; de Foe, J. D. The lithium aluminum hydride-aluminum chloride reduction of oximes. Tetrahedron Lett. 1963, 4, 629-634.
-
(1963)
Tetrahedron Lett.
, vol.4
, pp. 629-634
-
-
Rerick, M.N.1
Trottier, C.H.2
Daignault, R.A.3
De Foe, J.D.4
-
9
-
-
33947332955
-
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
-
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
-
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
-
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
-
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
-
14
-
-
84863000806
-
-
US 2003/0144297 A1
-
Verhoest, P. R.; Hoffman, R. L.; Corbett, J. W.; Ennis, M. D.; Frank, K. E.; Fu, J.-M. Substituted aryl 1, 4-pyrazine derivatives. US 2003/0144297 A1, 2003.
-
(2003)
Substituted Aryl 1, 4-pyrazine Derivatives
-
-
Verhoest, P.R.1
Hoffman, R.L.2
Corbett, J.W.3
Ennis, M.D.4
Frank, K.E.5
Fu, J.-M.6
-
15
-
-
34247266658
-
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
-
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
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