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Results: 1-21 |
Results: 21
Diels-Alder cycloaddition of novel buta-1,3-diene derivatives possessing a(diethoxyphosphinoyl)difluoromethyl unit
Authors: Yokomatsu, T Katayama, S Shibuya, S
Citation: T. Yokomatsu et al., Diels-Alder cycloaddition of novel buta-1,3-diene derivatives possessing a(diethoxyphosphinoyl)difluoromethyl unit, CHEM COMMUN, (18), 2001, pp. 1878-1879
Synthesis and evaluation of a difluoromethylene analogue of sphingomyelin as an inhibitor of sphingomyelinase
Authors: Yokomatsu, T Takechi, H Akiyama, T Shibuya, S Kominato, T Soeda, S Shimeno, H
Citation: T. Yokomatsu et al., Synthesis and evaluation of a difluoromethylene analogue of sphingomyelin as an inhibitor of sphingomyelinase, BIOORG MED, 11(10), 2001, pp. 1277-1280
Synthesis of allenic (alpha,alpha-difluoromethylene)phosphonates from propargylic tosylates and acetates
Authors: Yokomatsu, T Ichimura, A Kato, J Shibuya, S
Citation: T. Yokomatsu et al., Synthesis of allenic (alpha,alpha-difluoromethylene)phosphonates from propargylic tosylates and acetates, SYNLETT, (2), 2001, pp. 287-289
Diastereoselective synthesis of chiral beta-amino-alpha-hydroxy-H-phosphinates through hydrophosphinylation of alpha-amino aldehydes
Authors: Yamagishi, T Suemune, K Yokomatsu, T Shibuya, S
Citation: T. Yamagishi et al., Diastereoselective synthesis of chiral beta-amino-alpha-hydroxy-H-phosphinates through hydrophosphinylation of alpha-amino aldehydes, TETRAHEDR L, 42(30), 2001, pp. 5033-5036
Radical-mediated furanose ring reconstruction from 2 ',3 '-seco-uridine
Authors: Kumamoto, H Ogamino, J Tanaka, H Suzuki, H Haraguchi, K Miyasaka, T Yokomatsu, T Shibuya, S
Citation: H. Kumamoto et al., Radical-mediated furanose ring reconstruction from 2 ',3 '-seco-uridine, TETRAHEDRON, 57(16), 2001, pp. 3331-3341
The widespread effect of beta 1,4-galactosyltransferase on N-glycan processing
Authors: Fukuta, K Abe, R Yokomatsu, T Minowa, MT Takeuchi, M Asanagi, M Makino, T
Citation: K. Fukuta et al., The widespread effect of beta 1,4-galactosyltransferase on N-glycan processing, ARCH BIOCH, 392(1), 2001, pp. 79-86
Synthesis and evaluation of multisubstrate analogue inhibitors of purine nucleoside phosphorylases
Authors: Yokomatsu, T Hayakawa, Y Kihara, T Koyanagi, S Soeda, S Shimeno, H Shibuya, S
Citation: T. Yokomatsu et al., Synthesis and evaluation of multisubstrate analogue inhibitors of purine nucleoside phosphorylases, BIO MED CH, 8(11), 2000, pp. 2571-2579
Remodeling of sugar chain structures of human interferon-gamma
Authors: Fukuta, K Abe, R Yokomatsu, T Kono, N Asanagi, M Omae, F Minowa, MT Takeuchi, M Makino, T
Citation: K. Fukuta et al., Remodeling of sugar chain structures of human interferon-gamma, GLYCOBIOLOG, 10(4), 2000, pp. 421-430
Stereoselective C-glycosylation of 2,3-dideoxyribofuranosides controlled by the methylenephosphonothioate functional groups at the 3-position
Authors: Yokomatsu, T Sada, T Shimizu, T Shibuya, S
Citation: T. Yokomatsu et al., Stereoselective C-glycosylation of 2,3-dideoxyribofuranosides controlled by the methylenephosphonothioate functional groups at the 3-position, HETEROCYCLE, 52(2), 2000, pp. 515-518
Genetic engineering of CHO cells producing human interferon-gamma by transfection of sialyltransferases
Authors: Fukuta, K Yokomatsu, T Abe, R Asanagi, M Makino, T
Citation: K. Fukuta et al., Genetic engineering of CHO cells producing human interferon-gamma by transfection of sialyltransferases, GLYCOCON J, 17(12), 2000, pp. 895-904
Stereoselective reduction of cyclopropylalkaones possessing a difluoromethylenephosphonate group at the ring: Application to stereoselective synthesis of novel cyclopropane nucleotide analogues
Authors: Yokomatsu, T Yamagishi, T Suemune, K Abe, H Kihara, T Soeda, S Shimeno, H Shibuya, S
Citation: T. Yokomatsu et al., Stereoselective reduction of cyclopropylalkaones possessing a difluoromethylenephosphonate group at the ring: Application to stereoselective synthesis of novel cyclopropane nucleotide analogues, TETRAHEDRON, 56(37), 2000, pp. 7099-7108
Synthesis of aryldifluoromethylphosphonothioic acids from O,O-diethyl aryldifluoromethylphosphonothioates
Authors: Yokomatsu, T Takechi, H Murano, T Shibuya, S
Citation: T. Yokomatsu et al., Synthesis of aryldifluoromethylphosphonothioic acids from O,O-diethyl aryldifluoromethylphosphonothioates, J ORG CHEM, 65(18), 2000, pp. 5858-5861
Control of bisecting GlcNAc addition to N-linked sugar chains
Authors: Fukuta, K Abe, R Yokomatsu, T Omae, F Asanagi, M Makino, T
Citation: K. Fukuta et al., Control of bisecting GlcNAc addition to N-linked sugar chains, J BIOL CHEM, 275(31), 2000, pp. 23456-23461
Comparative study of the N-glycans of human monoclonal immunoglobulins M produced by hybridoma and parental cells
Authors: Fukuta, K Abe, R Yokomatsu, T Kono, N Nagatomi, Y Asanagi, M Shimazaki, Y Makino, T
Citation: K. Fukuta et al., Comparative study of the N-glycans of human monoclonal immunoglobulins M produced by hybridoma and parental cells, ARCH BIOCH, 378(1), 2000, pp. 142-150
Synthesis and biological evaluation of alpha,alpha-difluorobenzylphosphonic acid derivatives as small molecular inhibitors of protein-tyrosine phosphatase 1B
Authors: Yokomatsu, T Murano, T Umesue, I Soeda, S Shimeno, H Shibuya, S
Citation: T. Yokomatsu et al., Synthesis and biological evaluation of alpha,alpha-difluorobenzylphosphonic acid derivatives as small molecular inhibitors of protein-tyrosine phosphatase 1B, BIOORG MED, 9(4), 1999, pp. 529-532
Synthesis and biological evaluation of 1,1-difluoro-2-(tetrahydro-3-furanyl)ethylphosphonic acids possessing a N9-purinylmethyl functional group at the ring. A new class of inhibitors for purine nucleoside phosphorylases
Authors: Yokomatsu, T Hayakawa, Y Suemune, K Kihara, T Soeda, S Shimeno, H Shibuya, S
Citation: T. Yokomatsu et al., Synthesis and biological evaluation of 1,1-difluoro-2-(tetrahydro-3-furanyl)ethylphosphonic acids possessing a N9-purinylmethyl functional group at the ring. A new class of inhibitors for purine nucleoside phosphorylases, BIOORG MED, 9(19), 1999, pp. 2833-2836
Stereoselective synthesis of methylene phosphonate analogues of thymidine 3 '-phosphate and 2 '-deoxyuridine 3 '-phosphate via intramolecular N-glycosylation reaction of thioglycosides
Authors: Yokomatsu, T Shimizu, T Sada, T Shibuya, S
Citation: T. Yokomatsu et al., Stereoselective synthesis of methylene phosphonate analogues of thymidine 3 '-phosphate and 2 '-deoxyuridine 3 '-phosphate via intramolecular N-glycosylation reaction of thioglycosides, HETEROCYCLE, 50(1), 1999, pp. 21-25
Enantioselective synthesis of alpha-hydroxyphosphinic acid derivatives through hydrophosphinylation of aldehydes catalyzed by Al-Li-BINOL complex
Authors: Yamagishi, T Yokomatsu, T Suemune, K Shibuya, S
Citation: T. Yamagishi et al., Enantioselective synthesis of alpha-hydroxyphosphinic acid derivatives through hydrophosphinylation of aldehydes catalyzed by Al-Li-BINOL complex, TETRAHEDRON, 55(41), 1999, pp. 12125-12136
Highly diastereoselective synthesis of (6-methylenepyrrolo[1,2-c]oxazol-7-yl)- methylphosphonate by an application of radical reaction
Authors: Yuasa, Y Fujimaki, N Yokomatsu, T Ando, J Shibuya, S
Citation: Y. Yuasa et al., Highly diastereoselective synthesis of (6-methylenepyrrolo[1,2-c]oxazol-7-yl)- methylphosphonate by an application of radical reaction, SYN COMMUN, 29(20), 1999, pp. 3573-3580
Convenient synthesis of cyclopropylalkanol derivatives possessing a difluoromethylenephosphonate group at the ring
Authors: Yokomatsu, T Abe, H Yamagishi, T Suemune, K Shibuya, S
Citation: T. Yokomatsu et al., Convenient synthesis of cyclopropylalkanol derivatives possessing a difluoromethylenephosphonate group at the ring, J ORG CHEM, 64(22), 1999, pp. 8413-8418
Synthesis of 1,1-difluoro-5-(1H-9-purinyl)-2-pentenylphosphonic acids and the related methano analogues. Remarkable effect of the nucleobases and thecyclopropane rings on inhibitory activity toward purine nucleoside phosphorylase
Authors: Yokomatsu, T Abe, H Sato, M Suemune, K Kihara, T Soeda, S Shimeno, H Shibuya, S
Citation: T. Yokomatsu et al., Synthesis of 1,1-difluoro-5-(1H-9-purinyl)-2-pentenylphosphonic acids and the related methano analogues. Remarkable effect of the nucleobases and thecyclopropane rings on inhibitory activity toward purine nucleoside phosphorylase, BIO MED CH, 6(12), 1998, pp. 2495-2505
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