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Results: 1-13 |
Results: 13
A novel and efficient methodology for the C-C bond forming radical cyclization of hydrophobic substrates in water
Authors: Kita, Y Nambu, H Ramesh, NG Anilkumar, G Matsugi, M
Citation: Y. Kita et al., A novel and efficient methodology for the C-C bond forming radical cyclization of hydrophobic substrates in water, ORG LETT, 3(8), 2001, pp. 1157-1160
An efficient sulfenylation of aromatics using highly active quinone mono O,S-acetal bearing a pentafluorophenylthio group
Authors: Matsugi, M Murata, K Nambu, H Kita, Y
Citation: M. Matsugi et al., An efficient sulfenylation of aromatics using highly active quinone mono O,S-acetal bearing a pentafluorophenylthio group, TETRAHEDR L, 42(6), 2001, pp. 1077-1080
A novel determination method of the absolute configuration of 1-aryl-1-alkylalcohols and amines by an intramolecular CH/pi shielding effect in H-1 NMR
Authors: Matsugi, M Itoh, K Nojima, M Hagimoto, Y Kita, Y
Citation: M. Matsugi et al., A novel determination method of the absolute configuration of 1-aryl-1-alkylalcohols and amines by an intramolecular CH/pi shielding effect in H-1 NMR, TETRAHEDR L, 42(45), 2001, pp. 8019-8022
Determination of stereochemistry and separation of diastereomeric derivatives of trans-2-pyridylcyclohexanols by extraction
Authors: Matsugi, M Nojima, M Hagimoto, Y Kita, Y
Citation: M. Matsugi et al., Determination of stereochemistry and separation of diastereomeric derivatives of trans-2-pyridylcyclohexanols by extraction, TETRAHEDR L, 42(45), 2001, pp. 8039-8042
Determination of absolute configuration of trans-2-arylcyclohexanols usingremarkable aryl-induced H-1 NMR shifts in diastereomeric derivatives
Authors: Matsugi, M Itoh, K Nojima, M Hagimoto, Y Kita, Y
Citation: M. Matsugi et al., Determination of absolute configuration of trans-2-arylcyclohexanols usingremarkable aryl-induced H-1 NMR shifts in diastereomeric derivatives, TETRAHEDR L, 42(39), 2001, pp. 6903-6905
Catalytic asymmetric oxidation of sulfide with titanium-mandelic acid complex: practical synthesis of (S)-3-[1-(2-methylphenyl)imidazol-2-ylsulfinyl]propan-1-ol, the key intermediate of OPC-29030
Authors: Matsugi, M Fukuda, N Muguruma, Y Yamaguchi, T Minamikawa, J Otsuka, S
Citation: M. Matsugi et al., Catalytic asymmetric oxidation of sulfide with titanium-mandelic acid complex: practical synthesis of (S)-3-[1-(2-methylphenyl)imidazol-2-ylsulfinyl]propan-1-ol, the key intermediate of OPC-29030, TETRAHEDRON, 57(14), 2001, pp. 2739-2744
Facile and efficient sulfenylation method using quinone mono-O,S-acetals under mild conditions
Authors: Matsugi, M Murata, K Gotanda, K Nambu, H Anilkumar, G Matsumoto, K Kita, Y
Citation: M. Matsugi et al., Facile and efficient sulfenylation method using quinone mono-O,S-acetals under mild conditions, J ORG CHEM, 66(7), 2001, pp. 2434-2441
Regioselective nucleophilic addition of methoxybenzene derivatives to the beta-carbon of p-benzoquinone mono O,S-acetal
Authors: Matsugi, M Murata, K Anilkumar, G Nambu, H Kita, Y
Citation: M. Matsugi et al., Regioselective nucleophilic addition of methoxybenzene derivatives to the beta-carbon of p-benzoquinone mono O,S-acetal, CHEM PHARM, 49(12), 2001, pp. 1658-1659
Doebner-Miller synthesis in a two-phase system: practical preparation of quinolines
Authors: Matsugi, M Tabusa, F Minamikawa, J
Citation: M. Matsugi et al., Doebner-Miller synthesis in a two-phase system: practical preparation of quinolines, TETRAHEDR L, 41(44), 2000, pp. 8523-8525
Asymmetric Pummerer rearrangement and related reactions
Authors: Matsugi, M Shibata, N Kita, Y
Citation: M. Matsugi et al., Asymmetric Pummerer rearrangement and related reactions, ADV SULF CH, 2, 2000, pp. 215-248
Efficient stereoselective synthesis of alpha-C-glycopyranosides using 2,2 '-azobis(2,4-dimethyl-4-methoxyvaleronitrile) [V-70]
Authors: Gotanda, K Matsugi, M Suemura, M Ohira, C Sano, A Oka, M Kita, Y
Citation: K. Gotanda et al., Efficient stereoselective synthesis of alpha-C-glycopyranosides using 2,2 '-azobis(2,4-dimethyl-4-methoxyvaleronitrile) [V-70], TETRAHEDRON, 55(34), 1999, pp. 10315-10324
Radical addition reaction of brominated active methylene compounds to enolethers using 2,2 '-azobis(2,4-dimethyl-4-methoxyvaleronitrile) (V-70) as an initiator
Authors: Kita, Y Sano, A Yamaguchi, T Oka, M Gotanda, K Matsugi, M
Citation: Y. Kita et al., Radical addition reaction of brominated active methylene compounds to enolethers using 2,2 '-azobis(2,4-dimethyl-4-methoxyvaleronitrile) (V-70) as an initiator, J ORG CHEM, 64(2), 1999, pp. 675-678
Highly stereoselective synthesis of carbocycles via a radical addition reaction using 2,2 '-azobis(2,4-dimethyl-4-methoxyvaleronitrile) [V-70L]
Authors: Matsugi, M Gotanda, K Ohira, C Suemura, M Sano, A Kita, Y
Citation: M. Matsugi et al., Highly stereoselective synthesis of carbocycles via a radical addition reaction using 2,2 '-azobis(2,4-dimethyl-4-methoxyvaleronitrile) [V-70L], J ORG CHEM, 64(18), 1999, pp. 6928-6930
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