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Volumn 61, Issue , 2007, Pages 143-216

Deoxy Sugars: Occurrence and Synthesis

Author keywords

[No Author keywords available]

Indexed keywords

2 DEOXYRIBOSE; 2,6 DIDEOXY DEXTRO ARABINO HEXOSE; 2,6 DIDEOXY DEXTRO LYXO HEXOSE; 2,6 DIDEOXY DEXTRO RIBO HEXOSE; 2,6 DIDEOXY DEXTRO XYLO HEXOSE; 2,6 DIDEOXY LEVO ARABINO HEXOSE; 2,6 DIDEOXY LEVO LYXO HEXOSE; 2,6 DIDEOXY LEVO RIBO HEXOSE; 2,6 DIDEOXY LEVO XYLO HEXOSE; 3 DEOXY DEXTRO ERYTHROPENTOSE; 4 DEOXY DEXTRO ARABINO HEXOSE; 5 DEOXY DEXTRO XYLO HEXOSE; ANTINEOPLASTIC ANTIBIOTIC; ARABINOSE; BROMINE DERIVATIVE; CHROMOCICLOMYCIN; CHROMOMYCIN; DEOXYGLUCOSE; DEOXYSUGAR; DURHAMYCIN; GLUCONOLACTONASE; HEXOSE; MITHRAMYCIN; MONOSACCHARIDE; OLIGOSACCHARIDE; OLIVOMYCIN; PENTOSE; PYRANOSIDE; SULFONIC ACID DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 34948836804     PISSN: 00652318     EISSN: None     Source Type: Book Series    
DOI: 10.1016/S0065-2318(07)61004-X     Document Type: Review
Times cited : (100)

References (285)
  • 2
    • 0002334440 scopus 로고    scopus 로고
    • Chemical and biochemical aspects of deoxysugars and deoxysugar oligosaccharides
    • Kirschning A., Bechthold A.F.W., and Rohr J. Chemical and biochemical aspects of deoxysugars and deoxysugar oligosaccharides. Top. Curr. Chem. 188 (1997) 1-83
    • (1997) Top. Curr. Chem. , vol.188 , pp. 1-83
    • Kirschning, A.1    Bechthold, A.F.W.2    Rohr, J.3
  • 3
    • 0027998112 scopus 로고
    • Pathways and mechanisms in the biogenesis of novel deoxysugars by bacteria
    • Liu H.W., and Thorson J.S. Pathways and mechanisms in the biogenesis of novel deoxysugars by bacteria. Annu. Rev. Microbiol. 48 (1994) 223-256
    • (1994) Annu. Rev. Microbiol. , vol.48 , pp. 223-256
    • Liu, H.W.1    Thorson, J.S.2
  • 4
    • 0034693085 scopus 로고    scopus 로고
    • The synthesis of 2-deoxy-glycosides: 1988-1999
    • Marzabadi C., and Franck R.W. The synthesis of 2-deoxy-glycosides: 1988-1999. Tetrahedron 56 (2000) 8385-8417
    • (2000) Tetrahedron , vol.56 , pp. 8385-8417
    • Marzabadi, C.1    Franck, R.W.2
  • 5
    • 0035067443 scopus 로고    scopus 로고
    • Concepts for the total synthesis of deoxy sugars
    • Kirschning A., Jesberger M., and Schoning K.U. Concepts for the total synthesis of deoxy sugars. Synthesis (2001) 507-540
    • (2001) Synthesis , pp. 507-540
    • Kirschning, A.1    Jesberger, M.2    Schoning, K.U.3
  • 6
    • 11144296792 scopus 로고    scopus 로고
    • Natural occurring monosaccharides: Properties and synthesis
    • de Lederkremer R.M., and Gallo C. Natural occurring monosaccharides: Properties and synthesis. Adv. Carbohydr. Chem. 59 (2004) 9-67
    • (2004) Adv. Carbohydr. Chem. , vol.59 , pp. 9-67
    • de Lederkremer, R.M.1    Gallo, C.2
  • 7
    • 0025708075 scopus 로고
    • Derivatives of methyl β-lactoside as substrates for and inhibitors of β-d-galactosidase from E. coli
    • Bock K., and Adelhorst K. Derivatives of methyl β-lactoside as substrates for and inhibitors of β-d-galactosidase from E. coli. Carbohydr. Res. 202 (1990) 131-149
    • (1990) Carbohydr. Res. , vol.202 , pp. 131-149
    • Bock, K.1    Adelhorst, K.2
  • 8
    • 0033953349 scopus 로고    scopus 로고
    • Hydrolytic activity of α-galactosidases against deoxy derivatives of p-nitrophenyl α-d-galactopyranoside
    • Hakamata W., Nishio T., and Oku T. Hydrolytic activity of α-galactosidases against deoxy derivatives of p-nitrophenyl α-d-galactopyranoside. Carbohydr. Res. 324 (2000) 107-115
    • (2000) Carbohydr. Res. , vol.324 , pp. 107-115
    • Hakamata, W.1    Nishio, T.2    Oku, T.3
  • 9
    • 0037137274 scopus 로고    scopus 로고
    • Photoinduced electron transfer and chemical α-deoxygenation of d-galactono-1,4-lactone. Synthesis of 2-deoxy-d-lyxo-hexofuranosides
    • Chiocconi A., Marino C., Otal E., and de Lederkremer R.M. Photoinduced electron transfer and chemical α-deoxygenation of d-galactono-1,4-lactone. Synthesis of 2-deoxy-d-lyxo-hexofuranosides. Carbohydr. Res. 337 (2002) 2119-2126
    • (2002) Carbohydr. Res. , vol.337 , pp. 2119-2126
    • Chiocconi, A.1    Marino, C.2    Otal, E.3    de Lederkremer, R.M.4
  • 10
    • 11844260033 scopus 로고    scopus 로고
    • Synthesis of deoxy and acylamino derivatives of lactose and use of these for probing the active site of Neisseria meningitidis N-acetyltransferase
    • Westerlind U., Hagback P., Tidbäck B., Wiik L., Blixt O., Razi N., and Norberg T. Synthesis of deoxy and acylamino derivatives of lactose and use of these for probing the active site of Neisseria meningitidis N-acetyltransferase. Carbohydr. Res. 340 (2005) 221-233
    • (2005) Carbohydr. Res. , vol.340 , pp. 221-233
    • Westerlind, U.1    Hagback, P.2    Tidbäck, B.3    Wiik, L.4    Blixt, O.5    Razi, N.6    Norberg, T.7
  • 11
    • 0028762189 scopus 로고
    • Synthesis of allyl 3-deoxy- and 4-deoxy-β-d-galactopyranoside and simultaneous preparation of Gal(1→2)- and Gal(1→3)-linked disaccharide
    • Lee T., and Lee Y.C. Synthesis of allyl 3-deoxy- and 4-deoxy-β-d-galactopyranoside and simultaneous preparation of Gal(1→2)- and Gal(1→3)-linked disaccharide. Carbohydr. Res. 251 (1994) 69-79
    • (1994) Carbohydr. Res. , vol.251 , pp. 69-79
    • Lee, T.1    Lee, Y.C.2
  • 12
    • 0000268417 scopus 로고    scopus 로고
    • Direct halogenation of carbohydrate derivatives
    • Hanessian S. (Ed), Marcel Dekker, Inc., New York
    • Szarek W.A., and Kong X. Direct halogenation of carbohydrate derivatives. In: Hanessian S. (Ed). Preparative Carbohydrate Chemistry (1997), Marcel Dekker, Inc., New York 105-126
    • (1997) Preparative Carbohydrate Chemistry , pp. 105-126
    • Szarek, W.A.1    Kong, X.2
  • 14
    • 11144336397 scopus 로고
    • The reduction of chlorodeoxy sugars by tributyltin hydride
    • Arita H., Ueda N., and Matsushima Y. The reduction of chlorodeoxy sugars by tributyltin hydride. Bull. Chem. Soc. Jpn. 45 (1972) 567-569
    • (1972) Bull. Chem. Soc. Jpn. , vol.45 , pp. 567-569
    • Arita, H.1    Ueda, N.2    Matsushima, Y.3
  • 15
    • 0002387959 scopus 로고
    • Desulfonyloxylations of some secondary p-toluenesulfonates of glycosides by lithium triethylborohydride; a high-yielding route to 2- and 3-deoxy sugars
    • Baer H.H., and Hanna H.R. Desulfonyloxylations of some secondary p-toluenesulfonates of glycosides by lithium triethylborohydride; a high-yielding route to 2- and 3-deoxy sugars. Carbohydr. Res. 110 (1982) 19-41
    • (1982) Carbohydr. Res. , vol.110 , pp. 19-41
    • Baer, H.H.1    Hanna, H.R.2
  • 16
    • 0344902741 scopus 로고
    • A new method for the deoxygenation of secondary alcohols
    • Barton D.H.R., and McCombie S.W. A new method for the deoxygenation of secondary alcohols. J. Chem. Soc. Perkin I (1974) 1574-1585
    • (1974) J. Chem. Soc. Perkin I , pp. 1574-1585
    • Barton, D.H.R.1    McCombie, S.W.2
  • 17
    • 0036498808 scopus 로고    scopus 로고
    • Efficient synthesis of 2-deoxy-l-erythro-pentose (2-deoxy-l-ribose) from l-arabinose
    • Chong Y., and Chu C.K. Efficient synthesis of 2-deoxy-l-erythro-pentose (2-deoxy-l-ribose) from l-arabinose. Carbohydr. Res. 337 (2002) 397-402
    • (2002) Carbohydr. Res. , vol.337 , pp. 397-402
    • Chong, Y.1    Chu, C.K.2
  • 18
    • 0011430335 scopus 로고
    • Radical reactions in organic synthesis
    • Ramaiah M. Radical reactions in organic synthesis. Tetrahedron 43 (1987) 3541-3676
    • (1987) Tetrahedron , vol.43 , pp. 3541-3676
    • Ramaiah, M.1
  • 19
    • 0025316936 scopus 로고
    • On the mechanism of deoxygenation of secondary alcohols by tin hydride reduction of methyl xanthates and thiocarbonyl derivatives
    • Barton D.H.R., Jang D.O., and Cs. Jaszberenyi J. On the mechanism of deoxygenation of secondary alcohols by tin hydride reduction of methyl xanthates and thiocarbonyl derivatives. Tetrahedron Lett. 31 (1990) 3991-3994
    • (1990) Tetrahedron Lett. , vol.31 , pp. 3991-3994
    • Barton, D.H.R.1    Jang, D.O.2    Cs. Jaszberenyi, J.3
  • 20
    • 0000982459 scopus 로고
    • Tris(trimethylsilyl)silane-A new reducing agent
    • Chatgilialoglu C. Tris(trimethylsilyl)silane-A new reducing agent. J. Org. Chem. 53 (1988) 3641-3642
    • (1988) J. Org. Chem. , vol.53 , pp. 3641-3642
    • Chatgilialoglu, C.1
  • 21
    • 0000829322 scopus 로고
    • Organosilanes as radical-based reducing agents in synthesis
    • Chatgilialoglu C. Organosilanes as radical-based reducing agents in synthesis. Acc. Chem. Res. 25 (1992) 188-194
    • (1992) Acc. Chem. Res. , vol.25 , pp. 188-194
    • Chatgilialoglu, C.1
  • 22
    • 0027291622 scopus 로고
    • The invention of radical reactions. Part XXXI. Diphenylsilane: A reagent for deoxygenation of alcohols via their thiocarbonyl derivatives, deamination via isonitriles, and dehalogenation of bromo- and iodo-compounds by radical chain chemistry
    • Barton D.H.R., Jang D.O., and Cs. Jaszberenyi J. The invention of radical reactions. Part XXXI. Diphenylsilane: A reagent for deoxygenation of alcohols via their thiocarbonyl derivatives, deamination via isonitriles, and dehalogenation of bromo- and iodo-compounds by radical chain chemistry. Tetrahedron 49 (1993) 7193-7214
    • (1993) Tetrahedron , vol.49 , pp. 7193-7214
    • Barton, D.H.R.1    Jang, D.O.2    Cs. Jaszberenyi, J.3
  • 23
    • 84918694212 scopus 로고
    • Radical deoxygenation of secondary and primary alcohols with phenylsilane
    • Barton D.H.R., Jang D.O., and Jaszberenyi J.Cs. Radical deoxygenation of secondary and primary alcohols with phenylsilane. Synlett (1991) 435-438
    • (1991) Synlett , pp. 435-438
    • Barton, D.H.R.1    Jang, D.O.2    Jaszberenyi, J.Cs.3
  • 24
    • 0027479919 scopus 로고
    • The invention of radical reactions. Part XXIX. Radical mono- and dideoxygenations with silanes
    • Barton D.H.R., Jang D.O., and Jaszberenyi J.Cs. The invention of radical reactions. Part XXIX. Radical mono- and dideoxygenations with silanes. Tetrahedron 49 (1993) 2793-2804
    • (1993) Tetrahedron , vol.49 , pp. 2793-2804
    • Barton, D.H.R.1    Jang, D.O.2    Jaszberenyi, J.Cs.3
  • 25
    • 0025125940 scopus 로고
    • Deoxygenation of alcohols by the reactions of their xanthate esters with triethylsilane: An alternative to tributyltin hydride in the Barton-McCombie reaction
    • Nicholas Kirwan J., Roberts B.P., and Willis C.R. Deoxygenation of alcohols by the reactions of their xanthate esters with triethylsilane: An alternative to tributyltin hydride in the Barton-McCombie reaction. Tetrahedron Lett. 31 (1990) 5093-5096
    • (1990) Tetrahedron Lett. , vol.31 , pp. 5093-5096
    • Nicholas Kirwan, J.1    Roberts, B.P.2    Willis, C.R.3
  • 26
    • 33751385486 scopus 로고
    • The invention of radical reactions. Radical deoxygenations, dehalogenations, and deaminations with dialkyl phosphites and hypophosphorous acid as hydrogen sources
    • Barton D.H.R., Jang D.O., and Cs. Jaszberenyi J. The invention of radical reactions. Radical deoxygenations, dehalogenations, and deaminations with dialkyl phosphites and hypophosphorous acid as hydrogen sources. J. Org. Chem. 58 (1993) 6838-6842
    • (1993) J. Org. Chem. , vol.58 , pp. 6838-6842
    • Barton, D.H.R.1    Jang, D.O.2    Cs. Jaszberenyi, J.3
  • 27
    • 0141905809 scopus 로고    scopus 로고
    • Deoxygenation of carbohydrates by thiol-catalysed radical-chain redox rearrangement of the derived benzylidene acetals
    • Dang H.-.-S., Roberts B.P., Sekhon J.S., and Smits T.M. Deoxygenation of carbohydrates by thiol-catalysed radical-chain redox rearrangement of the derived benzylidene acetals. Org. Biomol. Chem. 1 (2003) 1330-1341
    • (2003) Org. Biomol. Chem. , vol.1 , pp. 1330-1341
    • Dang, H.-.-S.1    Roberts, B.P.2    Sekhon, J.S.3    Smits, T.M.4
  • 28
    • 0035926304 scopus 로고    scopus 로고
    • Regioselectivity in the ring opening of 2-phenyl-1,3-dioxan-2-yl radicals derived from cyclic benzylidene acetals and comparison with deoxygenation of a carbohydrate diol via its cyclic thionocarbonate
    • Roberts B.P., and Smits T.M. Regioselectivity in the ring opening of 2-phenyl-1,3-dioxan-2-yl radicals derived from cyclic benzylidene acetals and comparison with deoxygenation of a carbohydrate diol via its cyclic thionocarbonate. Tetrahedron Lett. 42 (2001) 3663-3666
    • (2001) Tetrahedron Lett. , vol.42 , pp. 3663-3666
    • Roberts, B.P.1    Smits, T.M.2
  • 29
    • 0026544089 scopus 로고
    • Inhibition of glycolysis by 2-deoxygalactose in Saccharomyces cerevisiae
    • Lagunas R., and Moreno E. Inhibition of glycolysis by 2-deoxygalactose in Saccharomyces cerevisiae. Yeast 8 (1992) 107-115
    • (1992) Yeast , vol.8 , pp. 107-115
    • Lagunas, R.1    Moreno, E.2
  • 30
    • 0015310488 scopus 로고
    • Inhibition of the multiplication of enveloped RNA-viruses by glucosamine and 2-deoxy-d-glucose
    • Kaluza G., Scholtissek C., and Rott R.A. Inhibition of the multiplication of enveloped RNA-viruses by glucosamine and 2-deoxy-d-glucose. J. Gen. Virol. 14 (1972) 251-259
    • (1972) J. Gen. Virol. , vol.14 , pp. 251-259
    • Kaluza, G.1    Scholtissek, C.2    Rott, R.A.3
  • 31
    • 0030837832 scopus 로고    scopus 로고
    • Antifungal activity of 2-deoxy-d-glucose on Botrytis cinerea, Penicillium expansum, and Rhizopus stolonifer: Ultrastructural and cytochemical aspects
    • El-Ghaouth A., Wilson C.L., and Wisniewski M. Antifungal activity of 2-deoxy-d-glucose on Botrytis cinerea, Penicillium expansum, and Rhizopus stolonifer: Ultrastructural and cytochemical aspects. Phytopatology 87 (1997) 772-779
    • (1997) Phytopatology , vol.87 , pp. 772-779
    • El-Ghaouth, A.1    Wilson, C.L.2    Wisniewski, M.3
  • 32
    • 23044456402 scopus 로고    scopus 로고
    • 2-Deoxyglucose as an energy restriction mimetic agent: Effects on mammary carcinogenesis and on mammary tumor cell grouth in vitro
    • and references therein
    • Zhu Z., Jiang W., McGinley J.N., and Thompson H.J. 2-Deoxyglucose as an energy restriction mimetic agent: Effects on mammary carcinogenesis and on mammary tumor cell grouth in vitro. Cancer Res. 65 (2005) 7023-7030 and references therein
    • (2005) Cancer Res. , vol.65 , pp. 7023-7030
    • Zhu, Z.1    Jiang, W.2    McGinley, J.N.3    Thompson, H.J.4
  • 34
    • 0029739240 scopus 로고    scopus 로고
    • Glycals in organic synthesis: The evolution of comprehensive strategies for the assembly of oligosaccharides and glycoconjugates of biological consequence
    • Danishefsky S., and Bilodeau M. Glycals in organic synthesis: The evolution of comprehensive strategies for the assembly of oligosaccharides and glycoconjugates of biological consequence. Angew. Chem. Int. Ed. Engl. 35 (1996) 1380-1419
    • (1996) Angew. Chem. Int. Ed. Engl. , vol.35 , pp. 1380-1419
    • Danishefsky, S.1    Bilodeau, M.2
  • 35
    • 0000234345 scopus 로고
    • Direct preparation of 2-deoxy-d-glucopyranosides from glucals without Ferrier rearrangement
    • Bolitt V., Mioskowski C., Lee S.G., and Falck J.R. Direct preparation of 2-deoxy-d-glucopyranosides from glucals without Ferrier rearrangement. J. Org. Chem. 55 (1990) 5812-5813
    • (1990) J. Org. Chem. , vol.55 , pp. 5812-5813
    • Bolitt, V.1    Mioskowski, C.2    Lee, S.G.3    Falck, J.R.4
  • 37
    • 0000316365 scopus 로고
    • Synthesis of 2-deoxy sugars from glycals
    • Sabesan S., and Neira S. Synthesis of 2-deoxy sugars from glycals. J. Org. Chem. 56 (1991) 5468-5472
    • (1991) J. Org. Chem. , vol.56 , pp. 5468-5472
    • Sabesan, S.1    Neira, S.2
  • 38
    • 0002256476 scopus 로고    scopus 로고
    • Novel glycosidations of glycals using BCl3 or BBr3 as a promoter for catalytic and stereoselective syntheses of 2-deoxy-α-glycosides
    • Toshima K., Nagai H., Ushiki Y., and Matsumara S. Novel glycosidations of glycals using BCl3 or BBr3 as a promoter for catalytic and stereoselective syntheses of 2-deoxy-α-glycosides. Synlett (1998) 1007-1009
    • (1998) Synlett , pp. 1007-1009
    • Toshima, K.1    Nagai, H.2    Ushiki, Y.3    Matsumara, S.4
  • 39
    • 0001832181 scopus 로고    scopus 로고
    • Unusual reactions of enopyranuronates with hydroxy acid esters under ferrier conditions
    • Wieczorek E., and Thiem J. Unusual reactions of enopyranuronates with hydroxy acid esters under ferrier conditions. Synlett (1998) 467-468
    • (1998) Synlett , pp. 467-468
    • Wieczorek, E.1    Thiem, J.2
  • 40
    • 1842688302 scopus 로고    scopus 로고
    • Rhenium(V)-catalyzed synthesis of 2-deoxy-α-glycosides
    • Sherry B.D., Loy R.N., and Toste F.D. Rhenium(V)-catalyzed synthesis of 2-deoxy-α-glycosides. J. Am. Chem. Soc. 126 (2004) 4510-4511
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 4510-4511
    • Sherry, B.D.1    Loy, R.N.2    Toste, F.D.3
  • 41
    • 1042288189 scopus 로고    scopus 로고
    • Stereoselective palladium-catalyzed O-glycosylation using glycols
    • Kim H., Men H., and Lee C. Stereoselective palladium-catalyzed O-glycosylation using glycols. J. Am. Chem. Soc. 126 (2004) 1336-1337
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 1336-1337
    • Kim, H.1    Men, H.2    Lee, C.3
  • 42
    • 0032575219 scopus 로고    scopus 로고
    • Mercuration-reductive demercuration of glycals: A mild and convenient entry to 2-deoxy-sugars
    • Bettelli E., Cherubini P., D'Andrea P., Passacantilli P., and Piancatelli G. Mercuration-reductive demercuration of glycals: A mild and convenient entry to 2-deoxy-sugars. Tetrahedron 54 (1998) 6011-6018
    • (1998) Tetrahedron , vol.54 , pp. 6011-6018
    • Bettelli, E.1    Cherubini, P.2    D'Andrea, P.3    Passacantilli, P.4    Piancatelli, G.5
  • 43
    • 0034684527 scopus 로고    scopus 로고
    • A mild and easy one-pot procedure for the synthesis of 2-deoxysugars from glycals
    • Costantino V., Imperatore C., Fattorusso E., and Mangoni A. A mild and easy one-pot procedure for the synthesis of 2-deoxysugars from glycals. Tetrahedron Lett. 41 (2000) 9177-9180
    • (2000) Tetrahedron Lett. , vol.41 , pp. 9177-9180
    • Costantino, V.1    Imperatore, C.2    Fattorusso, E.3    Mangoni, A.4
  • 45
    • 0037842865 scopus 로고    scopus 로고
    • 2O/NaI/benzyl alcohol: A novel reagent system for regioselective hydration of glycals: Application in the synthesis of 1,6-dideoxynojirimycin
    • 2O/NaI/benzyl alcohol: A novel reagent system for regioselective hydration of glycals: Application in the synthesis of 1,6-dideoxynojirimycin. Tetrahedron Lett. 44 (2003) 5001-5004
    • (2003) Tetrahedron Lett. , vol.44 , pp. 5001-5004
    • Rani, S.1    Agarwal, A.2    Vankar, Y.D.3
  • 46
    • 4444319399 scopus 로고    scopus 로고
    • Catalytic ceric ammonium nitrate mediated synthesis of 2-deoxy-1-thioglycosides
    • Paul S., and Jayaraman N. Catalytic ceric ammonium nitrate mediated synthesis of 2-deoxy-1-thioglycosides. Carbohydr. Res. 339 (2004) 2197-2204
    • (2004) Carbohydr. Res. , vol.339 , pp. 2197-2204
    • Paul, S.1    Jayaraman, N.2
  • 47
    • 0000695695 scopus 로고
    • Synthesis of deoxy sugars. Deoxygenation by treatment with N,N′-thiocarbonyldiimidazole/tri-n-butylstannane
    • Rasmussen J.R., Slinger C.J., Kordish R.J., and Newman-Evans D.D. Synthesis of deoxy sugars. Deoxygenation by treatment with N,N′-thiocarbonyldiimidazole/tri-n-butylstannane. J. Org. Chem. 46 (1981) 4843-4846
    • (1981) J. Org. Chem. , vol.46 , pp. 4843-4846
    • Rasmussen, J.R.1    Slinger, C.J.2    Kordish, R.J.3    Newman-Evans, D.D.4
  • 48
    • 0003069867 scopus 로고
    • 2-deoxy-d-arabino-hexose, 2-deoxy-d-lyxo-hexose, and their (2R)-2-deuterio analogs
    • Margaret Y., Wong H., and Gray G.R. 2-deoxy-d-arabino-hexose, 2-deoxy-d-lyxo-hexose, and their (2R)-2-deuterio analogs. Carbohydr. Res. 80 (1980) 87-98
    • (1980) Carbohydr. Res. , vol.80 , pp. 87-98
    • Margaret, Y.1    Wong, H.2    Gray, G.R.3
  • 50
    • 0000962275 scopus 로고
    • Radical rearrangement of 2-O-(diphenylphosphoryl)glycosyl bromides. A new synthesis for 2-deoxy disaccharides and 2-deoxy ribonucleosides
    • Koch A., Lamberth C., Wetterich F., and Giese B. Radical rearrangement of 2-O-(diphenylphosphoryl)glycosyl bromides. A new synthesis for 2-deoxy disaccharides and 2-deoxy ribonucleosides. J. Org. Chem. 58 (1993) 1083-1089
    • (1993) J. Org. Chem. , vol.58 , pp. 1083-1089
    • Koch, A.1    Lamberth, C.2    Wetterich, F.3    Giese, B.4
  • 52
    • 0034703343 scopus 로고    scopus 로고
    • Stereocontrolled syntheses of deoxyribonucleosides via photoinduced electron-transfer deoxygenation of benzoyl-protected ribo- and arabinonucleosides
    • Wang Z., Prudhomme D.R., Buck J.R., Park M., and Rizzo C.J. Stereocontrolled syntheses of deoxyribonucleosides via photoinduced electron-transfer deoxygenation of benzoyl-protected ribo- and arabinonucleosides. J. Org. Chem. 65 (2000) 5969-5985
    • (2000) J. Org. Chem. , vol.65 , pp. 5969-5985
    • Wang, Z.1    Prudhomme, D.R.2    Buck, J.R.3    Park, M.4    Rizzo, C.J.5
  • 53
    • 0033548106 scopus 로고    scopus 로고
    • Synthesis and transglycosylase-inhibiting properties of a disaccharide analogue of moenomycin A lacking substitution at C-4 of unit F
    • Riedel S., Donnerstag A., Hennig L., Richter P.W., Hobert K., and van Heijenoort D.M. Synthesis and transglycosylase-inhibiting properties of a disaccharide analogue of moenomycin A lacking substitution at C-4 of unit F. Tetrahedron 55 (1999) 1921-1936
    • (1999) Tetrahedron , vol.55 , pp. 1921-1936
    • Riedel, S.1    Donnerstag, A.2    Hennig, L.3    Richter, P.W.4    Hobert, K.5    van Heijenoort, D.M.6
  • 54
    • 0028858247 scopus 로고
    • Studies in macrolide synthesis: A sequential aldol/glycosylation approach to the synthesis of concanamycin A
    • Paterson I., and McLeod M.D. Studies in macrolide synthesis: A sequential aldol/glycosylation approach to the synthesis of concanamycin A. Tetrahedron Lett. 36 (1995) 9065-9068
    • (1995) Tetrahedron Lett. , vol.36 , pp. 9065-9068
    • Paterson, I.1    McLeod, M.D.2
  • 55
    • 0028271079 scopus 로고
    • Utility of glycosyl phosphites as glycosyl donors-fructofuranosyl and 2-deoxyhexopyranosyl phosphites in glycoside bond formation
    • Muller T., Schneider R., and Schmidt R.R. Utility of glycosyl phosphites as glycosyl donors-fructofuranosyl and 2-deoxyhexopyranosyl phosphites in glycoside bond formation. Tetrahedron Lett. 35 (1994) 4763-4766
    • (1994) Tetrahedron Lett. , vol.35 , pp. 4763-4766
    • Muller, T.1    Schneider, R.2    Schmidt, R.R.3
  • 56
    • 0035512323 scopus 로고    scopus 로고
    • One-pot synthesis of 2-deoxy-β-oligosaccharides
    • Pongdee R., Wu B., and Sulikowski G.A. One-pot synthesis of 2-deoxy-β-oligosaccharides. Org. Lett. 3 (2001) 3523-3525
    • (2001) Org. Lett. , vol.3 , pp. 3523-3525
    • Pongdee, R.1    Wu, B.2    Sulikowski, G.A.3
  • 57
    • 0035891757 scopus 로고    scopus 로고
    • The first polymer-assisted solution-phase synthesis of deoxyglycosides
    • Kirschning A., Jesberger M., and Schönberger A. The first polymer-assisted solution-phase synthesis of deoxyglycosides. Org. Lett. 3 (2001) 3623-3626
    • (2001) Org. Lett. , vol.3 , pp. 3623-3626
    • Kirschning, A.1    Jesberger, M.2    Schönberger, A.3
  • 58
    • 0026082096 scopus 로고
    • 2-Deoxyglycosyl phosphorodithioates. A novel type of glycosyl donors. Efficient synthesis of 2′-deoxydisaccharides
    • Bielawska H., and Michalska M. 2-Deoxyglycosyl phosphorodithioates. A novel type of glycosyl donors. Efficient synthesis of 2′-deoxydisaccharides. J. Carbohydr. Chem. 10 (1991) 107-112
    • (1991) J. Carbohydr. Chem. , vol.10 , pp. 107-112
    • Bielawska, H.1    Michalska, M.2
  • 59
    • 0000467493 scopus 로고
    • A convenient 2-deoxy-α-d-glucopyranosylation reaction using dimethylphosphothionate method
    • Yamanoi T., and Inazu T.T. A convenient 2-deoxy-α-d-glucopyranosylation reaction using dimethylphosphothionate method. Chem. Lett. (1990) 849-852
    • (1990) Chem. Lett. , pp. 849-852
    • Yamanoi, T.1    Inazu, T.T.2
  • 60
    • 0021997784 scopus 로고
    • On cardioactive steroids. XVI. Stereoselective β-glycosylation of digitose: The synthesis of digitoxin
    • Wiesner K., Tsai T.Y.R., and Jin H. On cardioactive steroids. XVI. Stereoselective β-glycosylation of digitose: The synthesis of digitoxin. Helv. Chim. Acta 68 (1985) 300-314
    • (1985) Helv. Chim. Acta , vol.68 , pp. 300-314
    • Wiesner, K.1    Tsai, T.Y.R.2    Jin, H.3
  • 61
    • 0003049403 scopus 로고
    • Preparation of 2-deoxy-β-d-lyxo-hexosides (2-deoxy-β-d-galactosides)
    • Crich D., and Ritchie T.J. Preparation of 2-deoxy-β-d-lyxo-hexosides (2-deoxy-β-d-galactosides). Carbohydr. Res. 190 (1989) C3-C6
    • (1989) Carbohydr. Res. , vol.190
    • Crich, D.1    Ritchie, T.J.2
  • 62
    • 0001651721 scopus 로고
    • The use of alkoxy-substituted anomeric radicals for the construction of beta-glycosides
    • Kahne D., Yang D., Lim J.J., Miller R., and Paguaga E. The use of alkoxy-substituted anomeric radicals for the construction of beta-glycosides. J. Am. Chem. Soc. 110 (1988) 8716-8717
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 8716-8717
    • Kahne, D.1    Yang, D.2    Lim, J.J.3    Miller, R.4    Paguaga, E.5
  • 63
    • 85066087038 scopus 로고
    • An attempt at the direct construction of 2-deoxy-β-glycosidic linkages capitalizing on 2-deoxyglycopyranosyl diethyl phosphites as glycosyl donors
    • Hashimoto S.-i., Sano A., Sakamoto H., Nakajima M., Yanagiya Y., and Ikegami S. An attempt at the direct construction of 2-deoxy-β-glycosidic linkages capitalizing on 2-deoxyglycopyranosyl diethyl phosphites as glycosyl donors. Synlett (1995) 1271-1273
    • (1995) Synlett , pp. 1271-1273
    • Hashimoto, S.-i.1    Sano, A.2    Sakamoto, H.3    Nakajima, M.4    Yanagiya, Y.5    Ikegami, S.6
  • 64
    • 0021925003 scopus 로고
    • Synthesis of the E-D-C trisaccharide unit of aureolic acid cytostatics
    • and references therein
    • Thiem J., and Gerken M. Synthesis of the E-D-C trisaccharide unit of aureolic acid cytostatics. J. Org. Chem. 50 (1985) 954-958 and references therein
    • (1985) J. Org. Chem. , vol.50 , pp. 954-958
    • Thiem, J.1    Gerken, M.2
  • 65
    • 0030843605 scopus 로고    scopus 로고
    • Stereoselective synthesis of 2-deoxy-β-glycosides from glycal precursors. 2. Stereochemistry of glycosidation reactions of 2-thiophenyl- and 2-selenophenyl-α-d-gluco-pyranosyl donors
    • Roush W.R., Sebesta D.P., and James R.A. Stereoselective synthesis of 2-deoxy-β-glycosides from glycal precursors. 2. Stereochemistry of glycosidation reactions of 2-thiophenyl- and 2-selenophenyl-α-d-gluco-pyranosyl donors. Tetrahedron 53 (1997) 8837-8852
    • (1997) Tetrahedron , vol.53 , pp. 8837-8852
    • Roush, W.R.1    Sebesta, D.P.2    James, R.A.3
  • 66
    • 0002175708 scopus 로고
    • Selenium-mediated glycosidations: A selective synthesis of β-2-deoxyglycosides
    • Perez M., and Beau J.-M. Selenium-mediated glycosidations: A selective synthesis of β-2-deoxyglycosides. Tetrahedron Lett. 30 (1989) 75-78
    • (1989) Tetrahedron Lett. , vol.30 , pp. 75-78
    • Perez, M.1    Beau, J.-M.2
  • 67
    • 0034678005 scopus 로고    scopus 로고
    • 1,2-Seleno migrations in carbohydrate chemistry: Solution and solid-phase synthesis of 2-deoxy glycosides, orthoesters and allyl orthoesters
    • Nicolaou K.C., Mitchell H.J., Fylaktakidou K.C., Suzuki H., and Rodriguez R.H. 1,2-Seleno migrations in carbohydrate chemistry: Solution and solid-phase synthesis of 2-deoxy glycosides, orthoesters and allyl orthoesters. Angew. Chem. Int. Ed. Engl. 39 (2000) 1089-1093
    • (2000) Angew. Chem. Int. Ed. Engl. , vol.39 , pp. 1089-1093
    • Nicolaou, K.C.1    Mitchell, H.J.2    Fylaktakidou, K.C.3    Suzuki, H.4    Rodriguez, R.H.5
  • 70
    • 0002071020 scopus 로고
    • The synthesis of 2′deoxy-β-disaccharides: Novel approaches
    • Trumtel M., Tavecchia P., Veyrières A., and Sinaÿ P. The synthesis of 2′deoxy-β-disaccharides: Novel approaches. Carbohydr. Res. 191 (1989) 29-52
    • (1989) Carbohydr. Res. , vol.191 , pp. 29-52
    • Trumtel, M.1    Tavecchia, P.2    Veyrières, A.3    Sinaÿ, P.4
  • 71
    • 0025814857 scopus 로고
    • A stereospecific route to 2-deoxy-β-glycosides
    • Gervay J., and Danishefsky S. A stereospecific route to 2-deoxy-β-glycosides. J. Org. Chem. 56 (1991) 5448-5451
    • (1991) J. Org. Chem. , vol.56 , pp. 5448-5451
    • Gervay, J.1    Danishefsky, S.2
  • 72
    • 0027911141 scopus 로고
    • An electrophile-mediated cyclization on the 1,6-anhydro-d-glucopyranose framework
    • Leteux C., Veyrières A., and Robert F. An electrophile-mediated cyclization on the 1,6-anhydro-d-glucopyranose framework. Carbohydr. Res. 242 (1993) 119-130
    • (1993) Carbohydr. Res. , vol.242 , pp. 119-130
    • Leteux, C.1    Veyrières, A.2    Robert, F.3
  • 73
    • 37049089748 scopus 로고
    • An expeditious and stereocontrolled preparation of 2-azido-2-deoxy-β-d-glucopyranose derivatives from d-glucal
    • Tailler D., Jacquinet J.C., Noirot A.M., and Beau J.M. An expeditious and stereocontrolled preparation of 2-azido-2-deoxy-β-d-glucopyranose derivatives from d-glucal. J. Chem. Soc. Perkin Trans. I (1992) 3163-3164
    • (1992) J. Chem. Soc. Perkin Trans. I , pp. 3163-3164
    • Tailler, D.1    Jacquinet, J.C.2    Noirot, A.M.3    Beau, J.M.4
  • 74
    • 0033553134 scopus 로고    scopus 로고
    • A highly stereoselective synthesis of 2-deoxy-β-glycosides using 2-deoxy-2-iodo-glucopyranosyl acetate donors
    • Roush W.R., and Bennett C.E. A highly stereoselective synthesis of 2-deoxy-β-glycosides using 2-deoxy-2-iodo-glucopyranosyl acetate donors. J. Am. Chem. Soc. 121 (1999) 3541-3542
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 3541-3542
    • Roush, W.R.1    Bennett, C.E.2
  • 75
    • 0033598252 scopus 로고    scopus 로고
    • 2-Deoxy-2-iodo- and 2-deoxy-2-bromo-α-glucopyranosyl trichloroacetimidates: Highly reactive and stereoselective donors for the synthesis of 2-deoxy-β-glycosides
    • Roush W.R., Gung B.W., and Bennett C.E. 2-Deoxy-2-iodo- and 2-deoxy-2-bromo-α-glucopyranosyl trichloroacetimidates: Highly reactive and stereoselective donors for the synthesis of 2-deoxy-β-glycosides. Org. Lett. 1 (1999) 891-893
    • (1999) Org. Lett. , vol.1 , pp. 891-893
    • Roush, W.R.1    Gung, B.W.2    Bennett, C.E.3
  • 76
    • 0033553134 scopus 로고    scopus 로고
    • A highly stereoselective synthesis of 2-deoxy-β-glycosides using 2-deoxy-2-iodo-glucopyranosyl acetate donors
    • Roush W.R., and Bennett C.E. A highly stereoselective synthesis of 2-deoxy-β-glycosides using 2-deoxy-2-iodo-glucopyranosyl acetate donors. J. Am. Chem. Soc. 121 (1999) 3541-3542
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 3541-3542
    • Roush, W.R.1    Bennett, C.E.2
  • 77
    • 0030843605 scopus 로고    scopus 로고
    • Stereoselective synthesis of 2-deoxy-β-glycosides from glycal precursors. 2. Stereochemistry of glycosidation reactions of 2-thiophenyl- and 2-selenophenyl-α-d-gluco-pyranosyl donors
    • Roush W.R., Sebesta D.P., and James R.A. Stereoselective synthesis of 2-deoxy-β-glycosides from glycal precursors. 2. Stereochemistry of glycosidation reactions of 2-thiophenyl- and 2-selenophenyl-α-d-gluco-pyranosyl donors. Tetrahedron 53 (1997) 8837-8852
    • (1997) Tetrahedron , vol.53 , pp. 8837-8852
    • Roush, W.R.1    Sebesta, D.P.2    James, R.A.3
  • 79
    • 0025998671 scopus 로고
    • Syntheses of β-2-deoxy-d-glycosides assisted by glycosidases
    • Petit J.-M., Paquet F., and Beau J.-M. Syntheses of β-2-deoxy-d-glycosides assisted by glycosidases. Tetrahedron Lett. 32 (1991) 6125-6128
    • (1991) Tetrahedron Lett. , vol.32 , pp. 6125-6128
    • Petit, J.-M.1    Paquet, F.2    Beau, J.-M.3
  • 80
    • 0035856626 scopus 로고    scopus 로고
    • Enzymatic synthesis of 2-deoxy-β-glucosides and stereochemistry of β-glycosidase from Sulfolobus solfataricus on glucal
    • Trincone A., Pagnotta E., Rossi M., Mazzone M., and Moracci M. Enzymatic synthesis of 2-deoxy-β-glucosides and stereochemistry of β-glycosidase from Sulfolobus solfataricus on glucal. Tetrahedron Asymmetry 12 (2001) 2783-2787
    • (2001) Tetrahedron Asymmetry , vol.12 , pp. 2783-2787
    • Trincone, A.1    Pagnotta, E.2    Rossi, M.3    Mazzone, M.4    Moracci, M.5
  • 81
    • 1842388691 scopus 로고
    • A convenient synthesis of 3-deoxy-d-erythro-pentose
    • Witczak Z., and Whistler R.L. A convenient synthesis of 3-deoxy-d-erythro-pentose. Carbohydr. Res. 110 (1982) 326-329
    • (1982) Carbohydr. Res. , vol.110 , pp. 326-329
    • Witczak, Z.1    Whistler, R.L.2
  • 82
    • 0027318961 scopus 로고
    • Biological roles of oligosaccharides: All of the theories are correct
    • Varki A. Biological roles of oligosaccharides: All of the theories are correct. Glycobiology 3 (1993) 97-130
    • (1993) Glycobiology , vol.3 , pp. 97-130
    • Varki, A.1
  • 83
    • 0028041301 scopus 로고
    • Selectin ligands
    • Varki A. Selectin ligands. Proc. Natl. Acad. Sci. 91 (1994) 7390-7397
    • (1994) Proc. Natl. Acad. Sci. , vol.91 , pp. 7390-7397
    • Varki, A.1
  • 84
    • 0034234658 scopus 로고    scopus 로고
    • Functional diversity in the trans-sialidase and mucin families in Trypanosoma cruzi
    • Frash A.C.C. Functional diversity in the trans-sialidase and mucin families in Trypanosoma cruzi. Parasitol. Today 16 (2000) 282-286
    • (2000) Parasitol. Today , vol.16 , pp. 282-286
    • Frash, A.C.C.1
  • 85
    • 12944279744 scopus 로고    scopus 로고
    • From glycoside hydrolases to thioglycoligases: The synthesis of thioglycosides
    • Stick R.V., and Stubbs K.A. From glycoside hydrolases to thioglycoligases: The synthesis of thioglycosides. Tetrahedron Asymmetry 16 (2005) 321-335
    • (2005) Tetrahedron Asymmetry , vol.16 , pp. 321-335
    • Stick, R.V.1    Stubbs, K.A.2
  • 86
    • 84971064239 scopus 로고
    • A synthesis of abequose (3,6-dideoxy-d-xylo-hexose)
    • Copeland C., and Stick R.V. A synthesis of abequose (3,6-dideoxy-d-xylo-hexose). Aust. J. Chem. 30 (1977) 1269-1273
    • (1977) Aust. J. Chem. , vol.30 , pp. 1269-1273
    • Copeland, C.1    Stick, R.V.2
  • 87
    • 0029119271 scopus 로고
    • Influence of monosaccharide derivatives on liver cell glycosaminoglycan synthesis: 3-Deoxy-d-xylo-hexose (3-deoxy-d-galactose) and methyl(methyl 4-chloro-4-deoxy-β-d-galactopyranosid)uronate
    • Thomas S.S., Plenkiewicz J., Ison E.R., Bols M., Zou W., Szarek W.A., and Kisilevsky R. Influence of monosaccharide derivatives on liver cell glycosaminoglycan synthesis: 3-Deoxy-d-xylo-hexose (3-deoxy-d-galactose) and methyl(methyl 4-chloro-4-deoxy-β-d-galactopyranosid)uronate. Biochim. Biophys. Acta 1272 (1995) 37-48
    • (1995) Biochim. Biophys. Acta , vol.1272 , pp. 37-48
    • Thomas, S.S.1    Plenkiewicz, J.2    Ison, E.R.3    Bols, M.4    Zou, W.5    Szarek, W.A.6    Kisilevsky, R.7
  • 88
    • 0001588993 scopus 로고
    • β-Elimination in aldonolactones: A convenient synthesis of 2,4,6-tri-O-benzoyl-3-deoxy-d-arabino-hexono-1,5-lactone
    • de Lederkremer R.M., Litter M.I., and Sala L.F. β-Elimination in aldonolactones: A convenient synthesis of 2,4,6-tri-O-benzoyl-3-deoxy-d-arabino-hexono-1,5-lactone. Carbohydr. Res. 36 (1974) 185-187
    • (1974) Carbohydr. Res. , vol.36 , pp. 185-187
    • de Lederkremer, R.M.1    Litter, M.I.2    Sala, L.F.3
  • 89
    • 0012912392 scopus 로고
    • A new synthesis of 3-deoxy-d-arabino-hexose and its tautomeric equilibrium
    • Du Mortier C., and de Lederkremer R.M. A new synthesis of 3-deoxy-d-arabino-hexose and its tautomeric equilibrium. J. Carbohydr. Chem. 3 (1984) 219-228
    • (1984) J. Carbohydr. Chem. , vol.3 , pp. 219-228
    • Du Mortier, C.1    de Lederkremer, R.M.2
  • 91
    • 0021720382 scopus 로고
    • The base catalyzed rearrangement of some 6-bromo-2,6-dideoxyaldono-1,4-lactones. Preparation of l-digitoxose
    • Bock K., Lundt I., and Pedersen C. The base catalyzed rearrangement of some 6-bromo-2,6-dideoxyaldono-1,4-lactones. Preparation of l-digitoxose. Acta Chem. Scand. B 38 (1984) 555-561
    • (1984) Acta Chem. Scand. B , vol.38 , pp. 555-561
    • Bock, K.1    Lundt, I.2    Pedersen, C.3
  • 92
  • 93
    • 0032192090 scopus 로고    scopus 로고
    • The glycosyl aldonolactone approach for the synthesis of β-d-Galf-(1→3)-d-Manp and 3-deoxy-α-d-xylo-hexofuranosyl-(1→3)-d-Manp
    • Marino C., Chiocconi A., Varela O., and de Lederkremer R.M. The glycosyl aldonolactone approach for the synthesis of β-d-Galf-(1→3)-d-Manp and 3-deoxy-α-d-xylo-hexofuranosyl-(1→3)-d-Manp. Carbohydr. Res. 311 (1998) 183-189
    • (1998) Carbohydr. Res. , vol.311 , pp. 183-189
    • Marino, C.1    Chiocconi, A.2    Varela, O.3    de Lederkremer, R.M.4
  • 94
    • 0038722213 scopus 로고    scopus 로고
    • Structural and serological studies on a new 4-deoxy-d-arabino-hexose-containing O-specific polysaccharide from the lipopolysaccharide of Citrobacter braakii PCM 1531 (serogroup O6)
    • Katzenellenbogen E., Kocharova N.A., Zatonsky G.V., Witkowska D., Bogulska M., Shashkov A.S., Gamian A., and Knirel Y.A. Structural and serological studies on a new 4-deoxy-d-arabino-hexose-containing O-specific polysaccharide from the lipopolysaccharide of Citrobacter braakii PCM 1531 (serogroup O6). Eur. J. Biochem. 270 (2003) 2732-2738
    • (2003) Eur. J. Biochem. , vol.270 , pp. 2732-2738
    • Katzenellenbogen, E.1    Kocharova, N.A.2    Zatonsky, G.V.3    Witkowska, D.4    Bogulska, M.5    Shashkov, A.S.6    Gamian, A.7    Knirel, Y.A.8
  • 96
    • 0019803046 scopus 로고
    • Structural and serological analysis of Citrobacter-036-specific polysaccharide, the homopolymer of (β1-2)-linked 4-deoxy-d-arabino-hexopyranosyl units
    • Romanowska E., Romanowska A., Lugowski C., and Katzenellenbogen E. Structural and serological analysis of Citrobacter-036-specific polysaccharide, the homopolymer of (β1-2)-linked 4-deoxy-d-arabino-hexopyranosyl units. Eur. J. Biochem. 121 (1981) 119-123
    • (1981) Eur. J. Biochem. , vol.121 , pp. 119-123
    • Romanowska, E.1    Romanowska, A.2    Lugowski, C.3    Katzenellenbogen, E.4
  • 98
    • 0002106231 scopus 로고
    • A novel, reductive ring-opening of carbohydrate benzylidene acetals, with unusual regioselectivity
    • Garegg P.J., and Hultberg H. A novel, reductive ring-opening of carbohydrate benzylidene acetals, with unusual regioselectivity. Carbohydr. Res. 93 (1981) C10-C11
    • (1981) Carbohydr. Res. , vol.93
    • Garegg, P.J.1    Hultberg, H.2
  • 99
    • 0014464176 scopus 로고
    • Substitution sekundärer Tosylestergruppen durch Jod Synthese von 4-Desoxy- und 4,6-Didesoxy-d-xylo-hexose
    • Siewert G., and Westphal O. Substitution sekundärer Tosylestergruppen durch Jod Synthese von 4-Desoxy- und 4,6-Didesoxy-d-xylo-hexose. Liebigs Ann. Chem. 720 (1988) 161-170
    • (1988) Liebigs Ann. Chem. , vol.720 , pp. 161-170
    • Siewert, G.1    Westphal, O.2
  • 100
    • 0000641940 scopus 로고
    • Convenient and stereospecific synthesis of deoxy sugars. Reductive displacement of trifluoromethylsulfonates
    • Barrette E.P., and Goodman L. Convenient and stereospecific synthesis of deoxy sugars. Reductive displacement of trifluoromethylsulfonates. J. Org. Chem. 49 (1984) 176-178
    • (1984) J. Org. Chem. , vol.49 , pp. 176-178
    • Barrette, E.P.1    Goodman, L.2
  • 101
    • 0001590277 scopus 로고
    • The synthesis of methyl 4-O-(4-O-α-d-galactopyranosyl-β-d-galactopyranosyl)-β-d- glucopyranoside: The methyl β-glycoside of the trisaccharide related to Fabry's disease
    • Cox D.D., Metzner E.K., and Reist E.J. The synthesis of methyl 4-O-(4-O-α-d-galactopyranosyl-β-d-galactopyranosyl)-β-d- glucopyranoside: The methyl β-glycoside of the trisaccharide related to Fabry's disease. Carbohydr. Res. 63 (1978) 139-147
    • (1978) Carbohydr. Res. , vol.63 , pp. 139-147
    • Cox, D.D.1    Metzner, E.K.2    Reist, E.J.3
  • 102
    • 5444254547 scopus 로고    scopus 로고
    • Synthesis of 4-deoxy-l-(and d-)hexoses from chiral noncarbohydrate building blocks
    • Caputo R., De Nisco M., Festa P., Guaragna A., Palumbo G., and Pedatella S. Synthesis of 4-deoxy-l-(and d-)hexoses from chiral noncarbohydrate building blocks. J. Org. Chem. 69 (2004) 7033-7037
    • (2004) J. Org. Chem. , vol.69 , pp. 7033-7037
    • Caputo, R.1    De Nisco, M.2    Festa, P.3    Guaragna, A.4    Palumbo, G.5    Pedatella, S.6
  • 103
    • 0036532409 scopus 로고    scopus 로고
    • Preparation and reactions of 2-allyl-5-deoxymannose derivatives
    • Saleh T., and Rousseau G. Preparation and reactions of 2-allyl-5-deoxymannose derivatives. Tetrahedron 58 (2002) 2891-2897
    • (2002) Tetrahedron , vol.58 , pp. 2891-2897
    • Saleh, T.1    Rousseau, G.2
  • 104
    • 84918304208 scopus 로고
    • Deoxy sugars. 5-Deoxy-d-xylo-hexose
    • Overend W.G. Deoxy sugars. 5-Deoxy-d-xylo-hexose. Method. Carbohydr. Chem. 6 (1972) 173-176
    • (1972) Method. Carbohydr. Chem. , vol.6 , pp. 173-176
    • Overend, W.G.1
  • 105
    • 0018586625 scopus 로고
    • Synthese des 1-(5-désoxy-β-d-ribo-hexofuranosyl)cytosine et 1-(2,5-didésoxy-β-d-érythro-hexofuranosyl)cytosine, et de leurs phosphates. Contribution à l'étude de la spécificité d'une ribonucléotide-réductase de mammifère (rat)
    • David S., and De Sennyey G. Synthese des 1-(5-désoxy-β-d-ribo-hexofuranosyl)cytosine et 1-(2,5-didésoxy-β-d-érythro-hexofuranosyl)cytosine, et de leurs phosphates. Contribution à l'étude de la spécificité d'une ribonucléotide-réductase de mammifère (rat). Carbohydr. Res. 77 (1979) 79-97
    • (1979) Carbohydr. Res. , vol.77 , pp. 79-97
    • David, S.1    De Sennyey, G.2
  • 106
    • 0011287359 scopus 로고
    • Synthesis of homoribose (5-deoxy-d-allose) and homoadenosine
    • Ryan K.J., Arzoumanian H., Acton E.M., and Goodman L. Synthesis of homoribose (5-deoxy-d-allose) and homoadenosine. J. Org. Chem. 86 (1964) 2503-2508
    • (1964) J. Org. Chem. , vol.86 , pp. 2503-2508
    • Ryan, K.J.1    Arzoumanian, H.2    Acton, E.M.3    Goodman, L.4
  • 108
    • 0040569613 scopus 로고
    • Synthesis of 5-deoxy-d-xylo-hexose and 5-deoxy-l-arabino-hexose, and their conversion into adenine nucleosides
    • Szarek W.A., Ritchie R.G.S., and Vyas D.M. Synthesis of 5-deoxy-d-xylo-hexose and 5-deoxy-l-arabino-hexose, and their conversion into adenine nucleosides. Carbohydr. Res. 62 (1978) 89-103
    • (1978) Carbohydr. Res. , vol.62 , pp. 89-103
    • Szarek, W.A.1    Ritchie, R.G.S.2    Vyas, D.M.3
  • 109
    • 0021106319 scopus 로고
    • Synthesis of 1-(5-deoxy-β-d-arabino-hexofuranosyl)cytosine
    • Iwakawa M., Martin O.R., and Szarek W.A. Synthesis of 1-(5-deoxy-β-d-arabino-hexofuranosyl)cytosine. Carbohydr. Res. 121 (1983) 99-108
    • (1983) Carbohydr. Res. , vol.121 , pp. 99-108
    • Iwakawa, M.1    Martin, O.R.2    Szarek, W.A.3
  • 110
    • 0035180515 scopus 로고    scopus 로고
    • Radical-chain redox rearrangement of cyclic benzylidene acetals to benzoate esters in the presence of thiols
    • Roberts B.P., and Smits T.M. Radical-chain redox rearrangement of cyclic benzylidene acetals to benzoate esters in the presence of thiols. Tetrahedron Lett. 42 (2001) 137-140
    • (2001) Tetrahedron Lett. , vol.42 , pp. 137-140
    • Roberts, B.P.1    Smits, T.M.2
  • 111
    • 0344500808 scopus 로고    scopus 로고
    • Synthetic application of glucose isomerase: Isomerization of C-5-modified (2R,3R,4R)-configured hexoses into the corresponding 2-ketoses
    • Fechter M.H., and Stütz A.E. Synthetic application of glucose isomerase: Isomerization of C-5-modified (2R,3R,4R)-configured hexoses into the corresponding 2-ketoses. Carbohydr. Res. 319 (1999) 55-62
    • (1999) Carbohydr. Res. , vol.319 , pp. 55-62
    • Fechter, M.H.1    Stütz, A.E.2
  • 114
    • 0038336048 scopus 로고    scopus 로고
    • Two flavone C-glycosides from the style of Zea mays with glycation inhibitory activity
    • Suzuki R., Okada Y., and Okuyama T. Two flavone C-glycosides from the style of Zea mays with glycation inhibitory activity. J. Nat. Prod. 66 (2003) 564-565
    • (2003) J. Nat. Prod. , vol.66 , pp. 564-565
    • Suzuki, R.1    Okada, Y.2    Okuyama, T.3
  • 115
    • 45549113731 scopus 로고
    • Alternanthin C-glycosylated flavonoid from Alternanthera philoxeroides
    • Bing-nan Z., Gabor B., and Geoffrey A.C. Alternanthin C-glycosylated flavonoid from Alternanthera philoxeroides. Phytochemistry 27 (1988) 3633-3636
    • (1988) Phytochemistry , vol.27 , pp. 3633-3636
    • Bing-nan, Z.1    Gabor, B.2    Geoffrey, A.C.3
  • 116
    • 77956953736 scopus 로고
    • The sugars of the cardiac glycosides
    • Reichstein T., and Weiss E. The sugars of the cardiac glycosides. Adv. Carbohydr. Chem. 17 (1962) 65-120
    • (1962) Adv. Carbohydr. Chem. , vol.17 , pp. 65-120
    • Reichstein, T.1    Weiss, E.2
  • 118
    • 0025895057 scopus 로고
    • Isolation of digoxin-like immunoreactive factors from mammalian adrenal cortex
    • Shaikh I.M., Lau B.W., Siegfried B.A., and Valdes Jr. R. Isolation of digoxin-like immunoreactive factors from mammalian adrenal cortex. J. Biol. Chem. 266 (1991) 13672-13678
    • (1991) J. Biol. Chem. , vol.266 , pp. 13672-13678
    • Shaikh, I.M.1    Lau, B.W.2    Siegfried, B.A.3    Valdes Jr., R.4
  • 119
    • 0029882128 scopus 로고    scopus 로고
    • Deglycosylated products of endogenous digoxin-like immunoreactive factor in mammalian tissue
    • Qazzaz H.M., Goudy S.L., and Valdes Jr. R. Deglycosylated products of endogenous digoxin-like immunoreactive factor in mammalian tissue. J. Biol. Chem. 271 (1996) 8731-8737
    • (1996) J. Biol. Chem. , vol.271 , pp. 8731-8737
    • Qazzaz, H.M.1    Goudy, S.L.2    Valdes Jr., R.3
  • 121
    • 0034624465 scopus 로고    scopus 로고
    • Steroidal glycosides from the aerial part of Asclepias incarnate
    • Warashina T., and Noro T. Steroidal glycosides from the aerial part of Asclepias incarnate. Phytochemistry 53 (2000) 485-498
    • (2000) Phytochemistry , vol.53 , pp. 485-498
    • Warashina, T.1    Noro, T.2
  • 122
    • 0027986520 scopus 로고
    • Steroidal constituents from roots stem of Asclepias fruticosa
    • Abe F., Mori Y., and Yamauchi T. Steroidal constituents from roots stem of Asclepias fruticosa. Chem. Pharm. Bull. 42 (1994) 1777-1783
    • (1994) Chem. Pharm. Bull. , vol.42 , pp. 1777-1783
    • Abe, F.1    Mori, Y.2    Yamauchi, T.3
  • 124
    • 0033943342 scopus 로고    scopus 로고
    • Pregnane glycosides from the roots of Asclepias tuberosa
    • Abe F., and Yamauchi T. Pregnane glycosides from the roots of Asclepias tuberosa. Chem. Pharm. Bull. 48 (2000) 1017-1022
    • (2000) Chem. Pharm. Bull. , vol.48 , pp. 1017-1022
    • Abe, F.1    Yamauchi, T.2
  • 125
    • 37049087771 scopus 로고
    • Toxic constituents of the Asclepiadaceae. Structure elucidation of Sarcovimiside A-C, pregnane glycosides of Sarcostemma viminale
    • Vleggaar R., van Heerden F.R., and Anderson L.A.P. Toxic constituents of the Asclepiadaceae. Structure elucidation of Sarcovimiside A-C, pregnane glycosides of Sarcostemma viminale. J. Chem. Soc. Perkin Trans. I (1983) 483-487
    • (1983) J. Chem. Soc. Perkin Trans. I , pp. 483-487
    • Vleggaar, R.1    van Heerden, F.R.2    Anderson, L.A.P.3
  • 127
    • 1842789152 scopus 로고    scopus 로고
    • The dynamic structure of jadomycin B and the amino acid incorporation step of its biosynthesis
    • Rix U., Zheng J., Remsing Rix L.L., Greenwell L., Yang K., and Rohr J. The dynamic structure of jadomycin B and the amino acid incorporation step of its biosynthesis. J. Am. Chem. Soc. 126 (2004) 4496-4497
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 4496-4497
    • Rix, U.1    Zheng, J.2    Remsing Rix, L.L.3    Greenwell, L.4    Yang, K.5    Rohr, J.6
  • 128
    • 0036224507 scopus 로고    scopus 로고
    • Biosynthesis of the dideoxysugar component of jadomycin B: Genes in the jad cluster of Streptomyces venezuelae ISP5230 for l-digitoxose assembly and transfer to the angucycline aglycone
    • Wang L., White R.L., and Vining L.C. Biosynthesis of the dideoxysugar component of jadomycin B: Genes in the jad cluster of Streptomyces venezuelae ISP5230 for l-digitoxose assembly and transfer to the angucycline aglycone. Microbiology 148 (2002) 1091-1103
    • (2002) Microbiology , vol.148 , pp. 1091-1103
    • Wang, L.1    White, R.L.2    Vining, L.C.3
  • 129
    • 0020536850 scopus 로고
    • Evidence for a chromosomal location of the genes coding for chloramphenicol production in Streptomyces venezuelae
    • Ahmed Z.U., and Vining L.C. Evidence for a chromosomal location of the genes coding for chloramphenicol production in Streptomyces venezuelae. J. Bacteriol. 154 (1983) 239-244
    • (1983) J. Bacteriol. , vol.154 , pp. 239-244
    • Ahmed, Z.U.1    Vining, L.C.2
  • 130
    • 0034162983 scopus 로고    scopus 로고
    • Tetrocarcin A inhibibits mitochondrial function of Bcl-2 and suppresses its anti-apoptotic activity
    • and references therein
    • Nakashima T., Miura M., and Hara M. Tetrocarcin A inhibibits mitochondrial function of Bcl-2 and suppresses its anti-apoptotic activity. Cancer Res. 60 (2000) 1229-1235 and references therein
    • (2000) Cancer Res. , vol.60 , pp. 1229-1235
    • Nakashima, T.1    Miura, M.2    Hara, M.3
  • 131
    • 0020451795 scopus 로고
    • Tetrocarcins E1, E2, F and F-1, new antibiotics. Fermentation, isolation and characterization
    • Tamaoki T., Kasai M., Shirahata K., and Tomita F. Tetrocarcins E1, E2, F and F-1, new antibiotics. Fermentation, isolation and characterization. J. Antibiot. 35 (1982) 979-984
    • (1982) J. Antibiot. , vol.35 , pp. 979-984
    • Tamaoki, T.1    Kasai, M.2    Shirahata, K.3    Tomita, F.4
  • 132
    • 0034114286 scopus 로고    scopus 로고
    • Arisostatins A and B, new members of tetrocarcin class of antibiotics from Micromonospora sp. TP-A0316. II. Structure determination
    • Igarashi Y., Takagi K., Kan Y., Fujii K., Harada K., Furumai T., and Oki T. Arisostatins A and B, new members of tetrocarcin class of antibiotics from Micromonospora sp. TP-A0316. II. Structure determination. J. Antibiot. 53 (2000) 233-440
    • (2000) J. Antibiot. , vol.53 , pp. 233-440
    • Igarashi, Y.1    Takagi, K.2    Kan, Y.3    Fujii, K.4    Harada, K.5    Furumai, T.6    Oki, T.7
  • 133
    • 85008099373 scopus 로고
    • Studies on the constituents of the leaves of Cassia torosa Cav I. The structure of two new C-glycosylflavones
    • Kitanata S., Ogata K., and Takido M. Studies on the constituents of the leaves of Cassia torosa Cav I. The structure of two new C-glycosylflavones. Chem. Pharm. Bull. 37 (1989) 2441-2444
    • (1989) Chem. Pharm. Bull. , vol.37 , pp. 2441-2444
    • Kitanata, S.1    Ogata, K.2    Takido, M.3
  • 134
    • 0344994565 scopus 로고    scopus 로고
    • The biosynthesis of aureolic acid group antibiotic
    • Rohr J., Mendez C., and Salas J.A. The biosynthesis of aureolic acid group antibiotic. Bioorg. Chem. 27 (1998) 41-54
    • (1998) Bioorg. Chem. , vol.27 , pp. 41-54
    • Rohr, J.1    Mendez, C.2    Salas, J.A.3
  • 135
    • 1542319789 scopus 로고    scopus 로고
    • MtmMII-mediated C-methylation during biosynthesis of the antitumor drug mithramycin is essential for biological activity and DNA-drug interaction
    • Rodríguez D., Quirós L.M., and Salas J.A. MtmMII-mediated C-methylation during biosynthesis of the antitumor drug mithramycin is essential for biological activity and DNA-drug interaction. J. Biol. Chem. 279 (2004) 8149-8158
    • (2004) J. Biol. Chem. , vol.279 , pp. 8149-8158
    • Rodríguez, D.1    Quirós, L.M.2    Salas, J.A.3
  • 136
    • 1142290136 scopus 로고    scopus 로고
    • Aureolic acids: Similar antibiotics with different biosynthetic gene clusters
    • O'Connor S. Aureolic acids: Similar antibiotics with different biosynthetic gene clusters. Chem. Biol. 11 (2004) 8-10
    • (2004) Chem. Biol. , vol.11 , pp. 8-10
    • O'Connor, S.1
  • 137
    • 0031922403 scopus 로고    scopus 로고
    • UCH9, a new antitumor antibiotic produced by Streptomyces. II. Structure elucidation of UCH9 by mass and NMR spectroscopy
    • Katahira R., Uosaki Y., Ogawa H., Yamashita Y., Nakano H., and Yoshida M. UCH9, a new antitumor antibiotic produced by Streptomyces. II. Structure elucidation of UCH9 by mass and NMR spectroscopy. J. Antibiot. 51 (1998) 267-274
    • (1998) J. Antibiot. , vol.51 , pp. 267-274
    • Katahira, R.1    Uosaki, Y.2    Ogawa, H.3    Yamashita, Y.4    Nakano, H.5    Yoshida, M.6
  • 139
    • 0031690038 scopus 로고    scopus 로고
    • Identification of two genes from Streptomyces argillaceus encoding glycosyltransferases involved in transfer of a disaccharide during biosynthesis of the antitumor drug mithramycin
    • Fernandez E., Weissbach U., Sanchez Reillo C., Brana A.F., Mendez C., Rohr J., and Salas J.A. Identification of two genes from Streptomyces argillaceus encoding glycosyltransferases involved in transfer of a disaccharide during biosynthesis of the antitumor drug mithramycin. J. Bacteriol. 180 (1998) 4929-4937
    • (1998) J. Bacteriol. , vol.180 , pp. 4929-4937
    • Fernandez, E.1    Weissbach, U.2    Sanchez Reillo, C.3    Brana, A.F.4    Mendez, C.5    Rohr, J.6    Salas, J.A.7
  • 140
    • 0025180955 scopus 로고
    • NMR investigation of mithramycin A binding to d(ATGCAT)2: A comparative study with chromomycin A3
    • Banville D.L., Keniry M.A., and Shafer R.H. NMR investigation of mithramycin A binding to d(ATGCAT)2: A comparative study with chromomycin A3. Biochemistry 29 (1990) 9294-9304
    • (1990) Biochemistry , vol.29 , pp. 9294-9304
    • Banville, D.L.1    Keniry, M.A.2    Shafer, R.H.3
  • 141
    • 0027339380 scopus 로고
    • The sugars in chromomycin A3 stabilize the Mg(2+)-dimer complex
    • Silva D.J., Goodnow Jr R., and Kahne D. The sugars in chromomycin A3 stabilize the Mg(2+)-dimer complex. Biochemistry 32 (1993) 463-471
    • (1993) Biochemistry , vol.32 , pp. 463-471
    • Silva, D.J.1    Goodnow Jr, R.2    Kahne, D.3
  • 142
    • 21044441008 scopus 로고    scopus 로고
    • Elucidation of the glycosylation sequence of mithramycin biosynthesis: Isolation of 3A-deolivosylpremithramycin B and its conversion to premithramycin B by glycosyltransferase MtmGII
    • Nur-e-Alam M., Mendez C., Salas J.A., and Rohr J. Elucidation of the glycosylation sequence of mithramycin biosynthesis: Isolation of 3A-deolivosylpremithramycin B and its conversion to premithramycin B by glycosyltransferase MtmGII. Chembiochem. 6 (2005) 632-636
    • (2005) Chembiochem. , vol.6 , pp. 632-636
    • Nur-e-Alam, M.1    Mendez, C.2    Salas, J.A.3    Rohr, J.4
  • 143
    • 0038701795 scopus 로고    scopus 로고
    • A novel antitumor drug with improved therapeutic index, mithramycin SA, and demycarosyl-mithramycin SK: Three new products generated in the mithramycin producer Streptomyces argillaceus through combinatorial biosynthesis
    • Remsing L.L., Gonzalez A.M., Nur-e-Alam M., Fernandez-Lozano M.J., Brana A.F., Rix U., Oliveira M.A., Mendez C., Salas J.A., Rohr J., and Mithramycin S.K. A novel antitumor drug with improved therapeutic index, mithramycin SA, and demycarosyl-mithramycin SK: Three new products generated in the mithramycin producer Streptomyces argillaceus through combinatorial biosynthesis. J. Am. Chem. Soc. 125 (2003) 5745-5753
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 5745-5753
    • Remsing, L.L.1    Gonzalez, A.M.2    Nur-e-Alam, M.3    Fernandez-Lozano, M.J.4    Brana, A.F.5    Rix, U.6    Oliveira, M.A.7    Mendez, C.8    Salas, J.A.9    Rohr, J.10    Mithramycin, S.K.11
  • 144
    • 17944386473 scopus 로고    scopus 로고
    • Biosynthesis of the antitumor chromomycin A3 in Streptomyces griseus: Analysis of the gene cluster and rational design of novel chromomycin analogs
    • Menendez N., Nur-e-Alam M., Brana A.F., Rohr J., Salas J.A., and Mendez C. Biosynthesis of the antitumor chromomycin A3 in Streptomyces griseus: Analysis of the gene cluster and rational design of novel chromomycin analogs. Chem. Biol. 11 (2004) 21-32
    • (2004) Chem. Biol. , vol.11 , pp. 21-32
    • Menendez, N.1    Nur-e-Alam, M.2    Brana, A.F.3    Rohr, J.4    Salas, J.A.5    Mendez, C.6
  • 145
    • 4444222040 scopus 로고    scopus 로고
    • AknK is an l-2-deoxyfucosyltransferase in the biosynthesis of the anthracycline aclacinomycin A
    • and references therein
    • Lu W., Leimkuhler C., Oberthür M., Kahne D., and Walsh K. AknK is an l-2-deoxyfucosyltransferase in the biosynthesis of the anthracycline aclacinomycin A. Biochemistry 43 (2004) 4548-4558 and references therein
    • (2004) Biochemistry , vol.43 , pp. 4548-4558
    • Lu, W.1    Leimkuhler, C.2    Oberthür, M.3    Kahne, D.4    Walsh, K.5
  • 146
    • 0000388018 scopus 로고    scopus 로고
    • Anthracycline biosynthesis in Streptomyces galilaeus
    • Fujii I., and Ebizuka Y. Anthracycline biosynthesis in Streptomyces galilaeus. Chem. Rev. 97 (1997) 2511-2524
    • (1997) Chem. Rev. , vol.97 , pp. 2511-2524
    • Fujii, I.1    Ebizuka, Y.2
  • 147
    • 0037178274 scopus 로고    scopus 로고
    • Cloning and characterization of Streptomyces galilaeus aclacinomycins polyketide synthase (PKS) cluster
    • Raty K., Kantola J., Hautala A., Hakala J., Ylihonko K., and Mantsala P. Cloning and characterization of Streptomyces galilaeus aclacinomycins polyketide synthase (PKS) cluster. Gene 293 (2002) 115-122
    • (2002) Gene , vol.293 , pp. 115-122
    • Raty, K.1    Kantola, J.2    Hautala, A.3    Hakala, J.4    Ylihonko, K.5    Mantsala, P.6
  • 148
    • 33748904372 scopus 로고    scopus 로고
    • New anthracycline disaccharide. Synthesis of l-daunosaminyl-α(1→4)-2-deoxy-l-rhamnosyl and of l-daunosamyl-α(1→4)-2-deoxy-l-fucosyl daunorubicin analogues
    • Animati F., Arcamone F., Berettoni M., Cipollone A., Franciotti M., and Lombardi P. New anthracycline disaccharide. Synthesis of l-daunosaminyl-α(1→4)-2-deoxy-l-rhamnosyl and of l-daunosamyl-α(1→4)-2-deoxy-l-fucosyl daunorubicin analogues. J. Chem. Soc. Perkin Trans. I (1996) 1327-1329
    • (1996) J. Chem. Soc. Perkin Trans. I , pp. 1327-1329
    • Animati, F.1    Arcamone, F.2    Berettoni, M.3    Cipollone, A.4    Franciotti, M.5    Lombardi, P.6
  • 149
    • 0033532859 scopus 로고    scopus 로고
    • Scavenging byproducts in the sulfoxide glycosylation reaction: Application to the synthesis of ciclamycin 0
    • Gildersleeve J., Smith A., Sakurai K., Raghavan S., and Kahne D. Scavenging byproducts in the sulfoxide glycosylation reaction: Application to the synthesis of ciclamycin 0. J. Am. Chem. Soc. 121 (1999) 6176-6182
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 6176-6182
    • Gildersleeve, J.1    Smith, A.2    Sakurai, K.3    Raghavan, S.4    Kahne, D.5
  • 151
    • 0028060661 scopus 로고
    • Investigations of the biosynthesis and structural revision of landomycin A
    • Weber S., Zolke C., Rohr J., and Beale J.M. Investigations of the biosynthesis and structural revision of landomycin A. J. Org. Chem. 59 (1994) 4211-4214
    • (1994) J. Org. Chem. , vol.59 , pp. 4211-4214
    • Weber, S.1    Zolke, C.2    Rohr, J.3    Beale, J.M.4
  • 152
    • 3543033413 scopus 로고    scopus 로고
    • Studies on the synthesis of landomycin A. Synthesis of the originally assigned structure of the aglycone, landomycinone, and revision of structure
    • Roush W.R., and Neitz R.J. Studies on the synthesis of landomycin A. Synthesis of the originally assigned structure of the aglycone, landomycinone, and revision of structure. J. Org. Chem. 69 (2004) 4906-4912
    • (2004) J. Org. Chem. , vol.69 , pp. 4906-4912
    • Roush, W.R.1    Neitz, R.J.2
  • 153
    • 0033977621 scopus 로고    scopus 로고
    • Two new tailoring enzymes, a glycosyltransferase and oxygenase, involved in biosynthesis of the angucycline antibiotic urdamycin A in Streptomyces fradiae Tü2717
    • Faust B., Hoffmeister D., Weitnauer G., Westrich L., Haag S., Schneider P., Decker H., Kunzel E., Rohr J., and Bechthold A. Two new tailoring enzymes, a glycosyltransferase and oxygenase, involved in biosynthesis of the angucycline antibiotic urdamycin A in Streptomyces fradiae Tü2717. Microbiology 146 (2000) 147-154
    • (2000) Microbiology , vol.146 , pp. 147-154
    • Faust, B.1    Hoffmeister, D.2    Weitnauer, G.3    Westrich, L.4    Haag, S.5    Schneider, P.6    Decker, H.7    Kunzel, E.8    Rohr, J.9    Bechthold, A.10
  • 154
    • 0001636923 scopus 로고    scopus 로고
    • Angucyclines: Total syntheses, new structure and biosynthetic studies of an emerging new class of antibiotics
    • Rohn K., and Rohr J. Angucyclines: Total syntheses, new structure and biosynthetic studies of an emerging new class of antibiotics. Top. Curr. Chem. 188 (1997) 127-195
    • (1997) Top. Curr. Chem. , vol.188 , pp. 127-195
    • Rohn, K.1    Rohr, J.2
  • 156
    • 0025268291 scopus 로고
    • Structural and immunological properties of the phenolic glycolipids from Mycobacterium gastri and Mycobacterium kansasii
    • Gilleron M., Venisse A., Fournie J.J., Riviere M., Dupont M.A., Gas N., and Puzo G. Structural and immunological properties of the phenolic glycolipids from Mycobacterium gastri and Mycobacterium kansasii. Eur. J. Biochem. 189 (1990) 167-173
    • (1990) Eur. J. Biochem. , vol.189 , pp. 167-173
    • Gilleron, M.1    Venisse, A.2    Fournie, J.J.3    Riviere, M.4    Dupont, M.A.5    Gas, N.6    Puzo, G.7
  • 157
    • 0034862868 scopus 로고    scopus 로고
    • Functional analysis of OleY l-oleandrosyl 3-O-methyltransferase of the oleandomycin biosynthetic pathway in Streptomyces antibioticus
    • Rodriguez L., Rodriguez D., Olano C., Brana A.F., Mendez C., and Salas J.A. Functional analysis of OleY l-oleandrosyl 3-O-methyltransferase of the oleandomycin biosynthetic pathway in Streptomyces antibioticus. J. Bacteriol. 183 (2001) 5358-5363
    • (2001) J. Bacteriol. , vol.183 , pp. 5358-5363
    • Rodriguez, L.1    Rodriguez, D.2    Olano, C.3    Brana, A.F.4    Mendez, C.5    Salas, J.A.6
  • 158
    • 0030827941 scopus 로고    scopus 로고
    • Apoptolidin, a new apoptosis inducer in transformed cells from Nocardiopsis sp.
    • Kim J.W., Adachi H., Shin-ya K., Hayakawa Y., and Seto H. Apoptolidin, a new apoptosis inducer in transformed cells from Nocardiopsis sp. J. Antibiot. 50 (1997) 628-630
    • (1997) J. Antibiot. , vol.50 , pp. 628-630
    • Kim, J.W.1    Adachi, H.2    Shin-ya, K.3    Hayakawa, Y.4    Seto, H.5
  • 160
    • 25444462806 scopus 로고    scopus 로고
    • Enantioselective synthesis of apoptolidin sugars
    • Crimmins M.T., and Long A. Enantioselective synthesis of apoptolidin sugars. Org. Lett. 7 (2005) 4157-4160
    • (2005) Org. Lett. , vol.7 , pp. 4157-4160
    • Crimmins, M.T.1    Long, A.2
  • 163
    • 0034007775 scopus 로고    scopus 로고
    • Identification and expression of genes involved in biosynthesis of l-oleandrose and its intermediate l-olivose in the oleandomycin producer Streptomyces antibioticus
    • Aguirrezabalaga I., Olano C., Allende N., Rodriguez L., Braña A.F., Méndez C., and Salas J.A. Identification and expression of genes involved in biosynthesis of l-oleandrose and its intermediate l-olivose in the oleandomycin producer Streptomyces antibioticus. Antimicrob. Agents Chemother. 44 (2000) 1266-1275
    • (2000) Antimicrob. Agents Chemother. , vol.44 , pp. 1266-1275
    • Aguirrezabalaga, I.1    Olano, C.2    Allende, N.3    Rodriguez, L.4    Braña, A.F.5    Méndez, C.6    Salas, J.A.7
  • 164
    • 0036854694 scopus 로고    scopus 로고
    • Digitoxosyltetracenomycin C and glucosyltetracenomycin C, two novel elloramycin analogues obtained by exploring the sugar donor substrate specificity of glycosyltransferase ElmGT
    • Fischer C., Rodriguez L., Patallo E.P., Lipata F., Brana A.F., Mendez C., Salas J.A., and Rohr J. Digitoxosyltetracenomycin C and glucosyltetracenomycin C, two novel elloramycin analogues obtained by exploring the sugar donor substrate specificity of glycosyltransferase ElmGT. J. Nat. Prod. 65 (2002) 1685-1689
    • (2002) J. Nat. Prod. , vol.65 , pp. 1685-1689
    • Fischer, C.1    Rodriguez, L.2    Patallo, E.P.3    Lipata, F.4    Brana, A.F.5    Mendez, C.6    Salas, J.A.7    Rohr, J.8
  • 165
    • 0001017526 scopus 로고
    • Total synthesis of carbohydrates. 3. Efficient enantioselective syntheses of 2,6-dideoxyhexoses
    • Roush W.R., and Brown R.J. Total synthesis of carbohydrates. 3. Efficient enantioselective syntheses of 2,6-dideoxyhexoses. J. Org. Chem. 48 (1983) 5093-5101
    • (1983) J. Org. Chem. , vol.48 , pp. 5093-5101
    • Roush, W.R.1    Brown, R.J.2
  • 166
    • 0001185213 scopus 로고
    • Total synthesis of carbohydrates: Stereoselective syntheses of 2,6-dideoxy-d-arabino-hexose and 2,6-dideoxy-d-ribo-hexose
    • Roush W.R., and Brown R.J. Total synthesis of carbohydrates: Stereoselective syntheses of 2,6-dideoxy-d-arabino-hexose and 2,6-dideoxy-d-ribo-hexose. J. Org. Chem. 47 (1982) 1371-1373
    • (1982) J. Org. Chem. , vol.47 , pp. 1371-1373
    • Roush, W.R.1    Brown, R.J.2
  • 167
    • 0001162725 scopus 로고
    • On the steric course of the addition of diallylzinc onto α,β-dialkoxy chiral carbonyl compounds: Stereospecific synthesis of 2,6-dideoxysugars of the l-series
    • Fronza G., Fuganti C., Grasselli P., Pedrocchi-Fantoni G., and Zirotti C. On the steric course of the addition of diallylzinc onto α,β-dialkoxy chiral carbonyl compounds: Stereospecific synthesis of 2,6-dideoxysugars of the l-series. Tetrahedron Lett. 23 (1982) 4143-4146
    • (1982) Tetrahedron Lett. , vol.23 , pp. 4143-4146
    • Fronza, G.1    Fuganti, C.2    Grasselli, P.3    Pedrocchi-Fantoni, G.4    Zirotti, C.5
  • 168
    • 0034843824 scopus 로고    scopus 로고
    • Synthesis of all diastereomers of the 2-deoxypentoses and the 2,6-dideoxyhexoses from 2-phenyl-1,3-dioxan-5-one hydrate
    • Ulven T., and Carlsen P.H.J. Synthesis of all diastereomers of the 2-deoxypentoses and the 2,6-dideoxyhexoses from 2-phenyl-1,3-dioxan-5-one hydrate. Eur. J. Org. Chem. (2001) 3367-3374
    • (2001) Eur. J. Org. Chem. , pp. 3367-3374
    • Ulven, T.1    Carlsen, P.H.J.2
  • 169
    • 0038680323 scopus 로고    scopus 로고
    • Synthesis of 2,6-dideoxysugars via ring-closing olefinic metathesis
    • Andreana P.R., McLellan J.S., Chen Y., and Wang P.G. Synthesis of 2,6-dideoxysugars via ring-closing olefinic metathesis. Org. Lett. 4 (2002) 3875-3878
    • (2002) Org. Lett. , vol.4 , pp. 3875-3878
    • Andreana, P.R.1    McLellan, J.S.2    Chen, Y.3    Wang, P.G.4
  • 170
    • 0028111955 scopus 로고
    • Application of tellurium chemistry and sharpless asymmetric epoxidation to the synthesis of optically active boivinose
    • Pepito A.S., and Dittmer D.C. Application of tellurium chemistry and sharpless asymmetric epoxidation to the synthesis of optically active boivinose. J. Org. Chem. 59 (1994) 4311-4312
    • (1994) J. Org. Chem. , vol.59 , pp. 4311-4312
    • Pepito, A.S.1    Dittmer, D.C.2
  • 171
    • 0004856925 scopus 로고
    • 2,6-Dideoxy-d-ribo-hexose (digitoxose)
    • and references therein
    • Horton D., Cheung T.-M., and Weckerle W. 2,6-Dideoxy-d-ribo-hexose (digitoxose). Method. Carbohydr. Chem. 8 (1980) 195-199 and references therein
    • (1980) Method. Carbohydr. Chem. , vol.8 , pp. 195-199
    • Horton, D.1    Cheung, T.-M.2    Weckerle, W.3
  • 174
    • 34948838030 scopus 로고
    • Stereocontrolled conversion of allylic alcohols into vicinal cis-diol
    • Pauls H.W., and Fraser-Reid B. Stereocontrolled conversion of allylic alcohols into vicinal cis-diol. J. Carbohydr. Chem. 4 (1985) 1-14
    • (1985) J. Carbohydr. Chem. , vol.4 , pp. 1-14
    • Pauls, H.W.1    Fraser-Reid, B.2
  • 175
    • 0031691318 scopus 로고    scopus 로고
    • Practical synthesis of 2,6-dideoxy-d-lyxo-hexose ("2-deoxyfucose") from d-galactose
    • Schafer C.M., and Molinski T.F. Practical synthesis of 2,6-dideoxy-d-lyxo-hexose ("2-deoxyfucose") from d-galactose. Carbohydr. Res. 310 (1998) 223-228
    • (1998) Carbohydr. Res. , vol.310 , pp. 223-228
    • Schafer, C.M.1    Molinski, T.F.2
  • 176
    • 0029953345 scopus 로고    scopus 로고
    • Bengazoles C-G from the sponge Jaspis sp. Synthesis of the side chain and determination of absolute configuration
    • Searle P.A., Richter R.K., and Molinski T.F. Bengazoles C-G from the sponge Jaspis sp. Synthesis of the side chain and determination of absolute configuration. J. Org. Chem. 61 (1996) 4073-4079
    • (1996) J. Org. Chem. , vol.61 , pp. 4073-4079
    • Searle, P.A.1    Richter, R.K.2    Molinski, T.F.3
  • 177
    • 34948813198 scopus 로고
    • The synthesis and cytotoxic activity of 1,3,4-tri-O-acetyl-2,6-dideoxy-l-arabino- and -l-lyxo-hexopyranose
    • Hadfield A.F., Cunningham L., and Sartorelli A.C. The synthesis and cytotoxic activity of 1,3,4-tri-O-acetyl-2,6-dideoxy-l-arabino- and -l-lyxo-hexopyranose. Carbohydr. Res. 72 (1979) 93-104
    • (1979) Carbohydr. Res. , vol.72 , pp. 93-104
    • Hadfield, A.F.1    Cunningham, L.2    Sartorelli, A.C.3
  • 178
    • 0010415352 scopus 로고
    • The preparation of some bromodeoxy- and deoxy-hexoses from bromodeoxyaldonic acids
    • Bock K., Lundt I., and Pedersen C. The preparation of some bromodeoxy- and deoxy-hexoses from bromodeoxyaldonic acids. Carbohydr. Res. 90 (1981) 7-16
    • (1981) Carbohydr. Res. , vol.90 , pp. 7-16
    • Bock, K.1    Lundt, I.2    Pedersen, C.3
  • 179
    • 0026329440 scopus 로고
    • Preparation of 2-, 3-, and 4-deoxy derivatives of l-rhamnose, and derivatives of 2-azido-2-deoxy-l-rhamnose and 2,6-dideoxy-2-fluoro-l-glucose, for use in glycosylation reactions
    • Bols M., Lundt I., and Ottosen E.R. Preparation of 2-, 3-, and 4-deoxy derivatives of l-rhamnose, and derivatives of 2-azido-2-deoxy-l-rhamnose and 2,6-dideoxy-2-fluoro-l-glucose, for use in glycosylation reactions. Carbohydr. Res. 222 (1991) 141-149
    • (1991) Carbohydr. Res. , vol.222 , pp. 141-149
    • Bols, M.1    Lundt, I.2    Ottosen, E.R.3
  • 181
    • 0034856716 scopus 로고    scopus 로고
    • (Chemo)enzymatic synthesis of dTDP-activated 2,6-dideoxysugars as building blocks of polyketide antibiotics
    • Amann S., Dräger G., Rupprath C., Kirschning A., and Elling L. (Chemo)enzymatic synthesis of dTDP-activated 2,6-dideoxysugars as building blocks of polyketide antibiotics. Carbohydr. Res. 335 (2001) 23-32
    • (2001) Carbohydr. Res. , vol.335 , pp. 23-32
    • Amann, S.1    Dräger, G.2    Rupprath, C.3    Kirschning, A.4    Elling, L.5
  • 182
    • 34948840590 scopus 로고    scopus 로고
    • J. Thiem, in D. Horton, L.D. Hawkins, and G.J. McGarvey (Eds.), Approaches to deoxyoligosaccharides of antibiotics and cytostatics by stereoselective glycosylations, Trends in Synthetic Carbohydrate Chemistry, ACS Symp. Ser., American Chemical Society, Washington, 1989, pp. 131-149.
  • 183
    • 0025174915 scopus 로고
    • Syntheses of kijanimicin oligosaccharides
    • Thiem J., and Köpper S. Syntheses of kijanimicin oligosaccharides. Tetrahedron 46 (1990) 113-138
    • (1990) Tetrahedron , vol.46 , pp. 113-138
    • Thiem, J.1    Köpper, S.2
  • 184
    • 0028472772 scopus 로고
    • One-pot-synthesis of α-linked deoxy sugar trisaccharides
    • Köpper S., and Thiem J. One-pot-synthesis of α-linked deoxy sugar trisaccharides. Carbohydr. Res. 260 (1994) 219-232
    • (1994) Carbohydr. Res. , vol.260 , pp. 219-232
    • Köpper, S.1    Thiem, J.2
  • 185
    • 0025666662 scopus 로고
    • Application of substituent-controlled oxidative coupling of glycals in a synthesis and structural corroboration of ciclamycin 0: New possibilities for the construction of hybrid anthracyclines
    • Suzuki K., Sulikowski G.A., Friesen R.W., and Danishefsky S.J. Application of substituent-controlled oxidative coupling of glycals in a synthesis and structural corroboration of ciclamycin 0: New possibilities for the construction of hybrid anthracyclines. J. Am. Chem. Soc. 112 (1990) 8895-8902
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 8895-8902
    • Suzuki, K.1    Sulikowski, G.A.2    Friesen, R.W.3    Danishefsky, S.J.4
  • 186
    • 0027538622 scopus 로고
    • A one step synthesis of the ciclamycin trisaccharide
    • Raghavan S., and Kahne D. A one step synthesis of the ciclamycin trisaccharide. J. Am. Chem. Soc. 115 (1993) 1580-1581
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 1580-1581
    • Raghavan, S.1    Kahne, D.2
  • 187
    • 0033532859 scopus 로고    scopus 로고
    • Scavenging byproducts in the sulfoxide glycosylation reaction: Application to the synthesis of ciclamycin 0
    • Gildersleeve J., Smith A., Sakurai K., Raghavan S., and Kahne D. Scavenging byproducts in the sulfoxide glycosylation reaction: Application to the synthesis of ciclamycin 0. J. Am. Chem. Soc. 121 (1999) 6176-6182
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 6176-6182
    • Gildersleeve, J.1    Smith, A.2    Sakurai, K.3    Raghavan, S.4    Kahne, D.5
  • 188
    • 0038341685 scopus 로고    scopus 로고
    • Stereoselective synthesis of l-oliose trisaccharide via iterative alkynol cycloisomerization and acid-catalyzed glycosylation
    • McDonald F.E., and Wu M. Stereoselective synthesis of l-oliose trisaccharide via iterative alkynol cycloisomerization and acid-catalyzed glycosylation. Org. Lett. 4 (2002) 3979-3981
    • (2002) Org. Lett. , vol.4 , pp. 3979-3981
    • McDonald, F.E.1    Wu, M.2
  • 189
    • 0042853258 scopus 로고    scopus 로고
    • Stereoselective synthesis of functionalized precursors of the CDEF and CDE 2,6-dideoxy-tetra- and trisaccharide units of durhamycins A and B
    • Durham T.B., and Roush W.R. Stereoselective synthesis of functionalized precursors of the CDEF and CDE 2,6-dideoxy-tetra- and trisaccharide units of durhamycins A and B. Org. Lett. 5 (2003) 1875-1878
    • (2003) Org. Lett. , vol.5 , pp. 1875-1878
    • Durham, T.B.1    Roush, W.R.2
  • 190
    • 0025649761 scopus 로고
    • Components of bacterial polysaccharides
    • Lindberg B. Components of bacterial polysaccharides. Adv. Carbohydr. Chem. 48 (1990) 279-318
    • (1990) Adv. Carbohydr. Chem. , vol.48 , pp. 279-318
    • Lindberg, B.1
  • 191
    • 0001864188 scopus 로고
    • Bacterial polysaccharides
    • Aspinall G.O. (Ed), Academic Press, Inc., New York
    • Kenne L., and Lindberg B. Bacterial polysaccharides. In: Aspinall G.O. (Ed). The Polysaccharides Vol. 2 (1983), Academic Press, Inc., New York 287-363
    • (1983) The Polysaccharides , vol.2 , pp. 287-363
    • Kenne, L.1    Lindberg, B.2
  • 192
    • 0018289827 scopus 로고
    • Artificial Salmonella vaccines: O-Antigenic oligosaccharide-protein conjugates induce protection against infection with Salmonella typhimurium
    • Svenson S.B., Nurminen M., and Lindberg A.A. Artificial Salmonella vaccines: O-Antigenic oligosaccharide-protein conjugates induce protection against infection with Salmonella typhimurium. Infect Immun. 25 (1979) 863-872
    • (1979) Infect Immun. , vol.25 , pp. 863-872
    • Svenson, S.B.1    Nurminen, M.2    Lindberg, A.A.3
  • 193
    • 0019430771 scopus 로고
    • Artificial Salmonella vaccines: Salmonella typhimurium O-antigen-specific oligosaccharide-protein conjugates elicit protective antibodies in rabbits and mice
    • Svenson S.B., and Lindberg A.A. Artificial Salmonella vaccines: Salmonella typhimurium O-antigen-specific oligosaccharide-protein conjugates elicit protective antibodies in rabbits and mice. Infect Immun. 32 (1981) 490-496
    • (1981) Infect Immun. , vol.32 , pp. 490-496
    • Svenson, S.B.1    Lindberg, A.A.2
  • 194
    • 0019432642 scopus 로고
    • Artificial Salmonella vaccines: Salmonella typhimurium O-antigen-specific oligosaccharide-protein conjugates elicit opsonizing antibodies that enhance phagocytosis
    • Jorbeck H.J., Svenson S.B., and A Lindberg A. Artificial Salmonella vaccines: Salmonella typhimurium O-antigen-specific oligosaccharide-protein conjugates elicit opsonizing antibodies that enhance phagocytosis. Infect Immun. 32 (1981) 497-502
    • (1981) Infect Immun. , vol.32 , pp. 497-502
    • Jorbeck, H.J.1    Svenson, S.B.2    A Lindberg, A.3
  • 195
    • 0026484311 scopus 로고
    • Protection of mice against Salmonella typhimurium with an O-specific polysaccharide-protein conjugate vaccine
    • Watson D.C., Robbins J.B., and Szu S.C. Protection of mice against Salmonella typhimurium with an O-specific polysaccharide-protein conjugate vaccine. Infect Immun. 60 (1992) 4679-4686
    • (1992) Infect Immun. , vol.60 , pp. 4679-4686
    • Watson, D.C.1    Robbins, J.B.2    Szu, S.C.3
  • 196
    • 14844313692 scopus 로고    scopus 로고
    • Nitrogen-fixing bacterium Burkholderia brasiliensis produces a novel yersiniose A-containing O-polysaccharide
    • Mattos K.A., Todeschini A.R., Heise N., Jones C., Previato J.O., and Mendonça-Previato L. Nitrogen-fixing bacterium Burkholderia brasiliensis produces a novel yersiniose A-containing O-polysaccharide. Glycobiology 15 (2005) 313-321
    • (2005) Glycobiology , vol.15 , pp. 313-321
    • Mattos, K.A.1    Todeschini, A.R.2    Heise, N.3    Jones, C.4    Previato, J.O.5    Mendonça-Previato, L.6
  • 197
    • 0028223297 scopus 로고
    • Lipo-oligosaccharidic antigen from Mycobacterium gastri, complete structure of a novel C4-branched 3,6-dideoxy-alpha-xylo-hexopyranose
    • Gilleron M., Vercauteren J., and Puzo G. Lipo-oligosaccharidic antigen from Mycobacterium gastri, complete structure of a novel C4-branched 3,6-dideoxy-alpha-xylo-hexopyranose. Biochemistry 22 (1994) 1930-1937
    • (1994) Biochemistry , vol.22 , pp. 1930-1937
    • Gilleron, M.1    Vercauteren, J.2    Puzo, G.3
  • 198
    • 11144320397 scopus 로고    scopus 로고
    • Biosynthesis of colitose: Expression, purification, and mechanistic characterization of GDP-4-keto-6-deoxy-d-mannose-3-dehydrase (ColD) and GDP-l-colitose synthase (ColC)
    • Alam J., Beyer N., and Liu H..w. Biosynthesis of colitose: Expression, purification, and mechanistic characterization of GDP-4-keto-6-deoxy-d-mannose-3-dehydrase (ColD) and GDP-l-colitose synthase (ColC). Biochemistry 43 (2004) 16450-16460
    • (2004) Biochemistry , vol.43 , pp. 16450-16460
    • Alam, J.1    Beyer, N.2    Liu, H..w.3
  • 199
    • 0034500195 scopus 로고    scopus 로고
    • Novel enzymatic mechanisms in carbohydrate metabolism
    • He X., Agnihotri G., and Liu H.-w. Novel enzymatic mechanisms in carbohydrate metabolism. Chem. Rev. 100 (2000) 4615-4662
    • (2000) Chem. Rev. , vol.100 , pp. 4615-4662
    • He, X.1    Agnihotri, G.2    Liu, H.-w.3
  • 200
    • 0014171367 scopus 로고
    • Ascarosides and ascaroside esters in Ascaris lumbricoides (Nematoda)
    • Jezyk P.F., and Fairbairn D. Ascarosides and ascaroside esters in Ascaris lumbricoides (Nematoda). Comp. Biochem. Physiol. 23 (1967) 691-705
    • (1967) Comp. Biochem. Physiol. , vol.23 , pp. 691-705
    • Jezyk, P.F.1    Fairbairn, D.2
  • 201
    • 0027490492 scopus 로고
    • Characterization of novel fucosyl- and tyvelosyl-containing glycoconjugates from Trinchinela spiralis muscle stage larvae
    • Wisnewski N., McNeil M., Grieve R.B., and Wassom D.L. Characterization of novel fucosyl- and tyvelosyl-containing glycoconjugates from Trinchinela spiralis muscle stage larvae. Mol. Biochem. Parasitol. 61 (1993) 25-35
    • (1993) Mol. Biochem. Parasitol. , vol.61 , pp. 25-35
    • Wisnewski, N.1    McNeil, M.2    Grieve, R.B.3    Wassom, D.L.4
  • 204
    • 0025707962 scopus 로고
    • Synthesis of stereospecifically labelled 3,6-dideoxyhexoses
    • Russell R.N., Weigel T.M., Han O., and Liu H.-w. Synthesis of stereospecifically labelled 3,6-dideoxyhexoses. Carbohydr. Res. 201 (1990) 95-114
    • (1990) Carbohydr. Res. , vol.201 , pp. 95-114
    • Russell, R.N.1    Weigel, T.M.2    Han, O.3    Liu, H.-w.4
  • 205
    • 0036434883 scopus 로고    scopus 로고
    • Synthesis of three Salmonella epitopes for biosensor studies of carbohydrates-antibody interactions
    • Yu H.N., Ling Ch.-Ch., and Bundle D.R. Synthesis of three Salmonella epitopes for biosensor studies of carbohydrates-antibody interactions. Can. J. Chem. 80 (2002) 1131-1140
    • (2002) Can. J. Chem. , vol.80 , pp. 1131-1140
    • Yu, H.N.1    Ling, Ch.-Ch.2    Bundle, D.R.3
  • 208
    • 0000455282 scopus 로고
    • A facile synthesis of methyl 3,6-dideoxy-l-xylo-hexopyranoside (colitose)
    • Bundle D.R., and Josephson S. A facile synthesis of methyl 3,6-dideoxy-l-xylo-hexopyranoside (colitose). Can. J. Chem. 56 (1978) 2686-2690
    • (1978) Can. J. Chem. , vol.56 , pp. 2686-2690
    • Bundle, D.R.1    Josephson, S.2
  • 209
    • 0002142105 scopus 로고
    • β-Elimination in aldonolactones. Synthesis of 3,6-dideoxy-l-arabino-hexose (Ascarylose)
    • Varela O., Fernández Cirrelli A., and de Lederkremer R.M. β-Elimination in aldonolactones. Synthesis of 3,6-dideoxy-l-arabino-hexose (Ascarylose). Carbohydr. Res. 70 (1979) 27-35
    • (1979) Carbohydr. Res. , vol.70 , pp. 27-35
    • Varela, O.1    Fernández Cirrelli, A.2    de Lederkremer, R.M.3
  • 210
    • 85013511130 scopus 로고
    • A crystalline furanose derivative of ascarylose. Synthesis of 2,5-di-O-benzoyl-3,6-dideoxy-α-l-arabino-hexofuranose
    • Varela O., Fernandez Cirelli A., and de Lederkremer R.M. A crystalline furanose derivative of ascarylose. Synthesis of 2,5-di-O-benzoyl-3,6-dideoxy-α-l-arabino-hexofuranose. Carbohydr. Res. 83 (1980) 130-135
    • (1980) Carbohydr. Res. , vol.83 , pp. 130-135
    • Varela, O.1    Fernandez Cirelli, A.2    de Lederkremer, R.M.3
  • 211
    • 1542696546 scopus 로고
    • Synthèse et réactivite du méthyl-2-O-benzoyl-3-bromo-3,6-didésoxy-α-l-altropyr anoside et du méthyl-2-O-benzoyl-3-bromo-3,6-didésoxy-4-O-méthyl- α-l-altropyranoside
    • Florent J.C., Monneret C., and Khuong-Huu Q. Synthèse et réactivite du méthyl-2-O-benzoyl-3-bromo-3,6-didésoxy-α-l-altropyr anoside et du méthyl-2-O-benzoyl-3-bromo-3,6-didésoxy-4-O-méthyl- α-l-altropyranoside. Carbohydr. Res. 56 (1977) 301-314
    • (1977) Carbohydr. Res. , vol.56 , pp. 301-314
    • Florent, J.C.1    Monneret, C.2    Khuong-Huu, Q.3
  • 212
    • 0025167325 scopus 로고
    • A simple preparation of methyl 3,6-dideoxy-α-l-arabino-hexopyranoside via a photodeoxygenation
    • Jütten P., and Scharf H.-D. A simple preparation of methyl 3,6-dideoxy-α-l-arabino-hexopyranoside via a photodeoxygenation. J. Carbohydr. Chem. 9 (1990) 675-681
    • (1990) J. Carbohydr. Chem. , vol.9 , pp. 675-681
    • Jütten, P.1    Scharf, H.-D.2
  • 213
    • 0029884008 scopus 로고    scopus 로고
    • Structure of the O-specific polysaccharide of an Aeromonas trota strain cross-reactive with Vibrio cholerae O139 Bengal
    • Knirel Y.A., Senchenkova S.N., Jansson P.E., Weintraub A., Ansaruzzaman M., and Albert M.J. Structure of the O-specific polysaccharide of an Aeromonas trota strain cross-reactive with Vibrio cholerae O139 Bengal. Eur. J. Biochem. 238 (1996) 160-165
    • (1996) Eur. J. Biochem. , vol.238 , pp. 160-165
    • Knirel, Y.A.1    Senchenkova, S.N.2    Jansson, P.E.3    Weintraub, A.4    Ansaruzzaman, M.5    Albert, M.J.6
  • 215
    • 0029155854 scopus 로고
    • Structure of the capsular polysaccharide of Vibrio cholerae O139 synonym Bengal containing d-galactose 4,6-cyclophosphate
    • Knirel Y.A., Paredes L., Jansson P.-E., Weintraub A., Widmalm G., and Albert M.J. Structure of the capsular polysaccharide of Vibrio cholerae O139 synonym Bengal containing d-galactose 4,6-cyclophosphate. Eur. J. Biochem. 232 (1995) 391-396
    • (1995) Eur. J. Biochem. , vol.232 , pp. 391-396
    • Knirel, Y.A.1    Paredes, L.2    Jansson, P.-E.3    Weintraub, A.4    Widmalm, G.5    Albert, M.J.6
  • 216
    • 0033554437 scopus 로고    scopus 로고
    • The conformation of a rigid tetrasaccharide epitope in the capsular polysaccharide of Vibrio cholerae O139
    • Gunawardena S., Fiore C.R., Johnson J.A., and Bush C.A. The conformation of a rigid tetrasaccharide epitope in the capsular polysaccharide of Vibrio cholerae O139. Biochemistry 38 (1999) 12062-12071
    • (1999) Biochemistry , vol.38 , pp. 12062-12071
    • Gunawardena, S.1    Fiore, C.R.2    Johnson, J.A.3    Bush, C.A.4
  • 217
    • 0029609631 scopus 로고
    • Capsular polysaccharide-protein conjugate vaccines against Vibrio cholerae O139 Bengal
    • Johnson J.A., Joseph A., and Morris J.G. Capsular polysaccharide-protein conjugate vaccines against Vibrio cholerae O139 Bengal. Bull. Inst. Pasteur 93 (1995) 285-290
    • (1995) Bull. Inst. Pasteur , vol.93 , pp. 285-290
    • Johnson, J.A.1    Joseph, A.2    Morris, J.G.3
  • 218
    • 0030956942 scopus 로고    scopus 로고
    • Structure of the O-specific polysaccharide of Salmonella enterica ssp. Arizonae O50 (Arizona 9a,9b)
    • Senchenkova S.N., Shashkov A.S., Knirel Y.A., Schwarzmüller E., and Mayer H. Structure of the O-specific polysaccharide of Salmonella enterica ssp. Arizonae O50 (Arizona 9a,9b). Carbohydr. Res. 301 (1997) 61-67
    • (1997) Carbohydr. Res. , vol.301 , pp. 61-67
    • Senchenkova, S.N.1    Shashkov, A.S.2    Knirel, Y.A.3    Schwarzmüller, E.4    Mayer, H.5
  • 219
    • 0020667133 scopus 로고
    • Structural studies of the O-antigens from Salmonella greenside and Salmonella adelaide
    • Kenne L., Lindberg B., Söderholm E., Bundle D.R., and Griffith D.W. Structural studies of the O-antigens from Salmonella greenside and Salmonella adelaide. Carbohydr. Res. 111 (1983) 289-296
    • (1983) Carbohydr. Res. , vol.111 , pp. 289-296
    • Kenne, L.1    Lindberg, B.2    Söderholm, E.3    Bundle, D.R.4    Griffith, D.W.5
  • 220
    • 0019871652 scopus 로고
    • Structural studies of the O-specific side-chain of the lipopolysaccharide from Escherichia coli O55
    • Lindberg B., Lindh F., Lindberg J.L.A., and Svenson S.B. Structural studies of the O-specific side-chain of the lipopolysaccharide from Escherichia coli O55. Carbohydr. Res. 97 (1981) 105-112
    • (1981) Carbohydr. Res. , vol.97 , pp. 105-112
    • Lindberg, B.1    Lindh, F.2    Lindberg, J.L.A.3    Svenson, S.B.4
  • 221
    • 0141584110 scopus 로고
    • Synthesis of the colitose determinant of Escherichia coli 0111 and 3,6-di-O-(α-d-galactopyranosyl)-α-d-glucopyranoside
    • Iversen T., and Bundle D.R. Synthesis of the colitose determinant of Escherichia coli 0111 and 3,6-di-O-(α-d-galactopyranosyl)-α-d-glucopyranoside. Can. J. Chem. 60 (1982) 299-303
    • (1982) Can. J. Chem. , vol.60 , pp. 299-303
    • Iversen, T.1    Bundle, D.R.2
  • 222
    • 0030896629 scopus 로고    scopus 로고
    • Synthesis of colitose-containing oligosaccharide structures found in polysaccharides from Vibrio cholerae O139 synonym Bengal using thioglycoside donors
    • Oscarson S., Tedebark U., and Turek D. Synthesis of colitose-containing oligosaccharide structures found in polysaccharides from Vibrio cholerae O139 synonym Bengal using thioglycoside donors. Carbohydr. Res. 299 (1997) 159-164
    • (1997) Carbohydr. Res. , vol.299 , pp. 159-164
    • Oscarson, S.1    Tedebark, U.2    Turek, D.3
  • 223
    • 0028036962 scopus 로고
    • Novel tyvelose-containing tri- and tetra-antennary N-glycans in the immunodominant antigens of the intracellular parasite Trichinella spiralis
    • Reason A.J., Ellis L.A., Appleton J.A., Wisnewski N., Grieve R.B., McNeil M., Wassom D.L., Morris H.R., and Dell A. Novel tyvelose-containing tri- and tetra-antennary N-glycans in the immunodominant antigens of the intracellular parasite Trichinella spiralis. Glycobiology 4 (1994) 593-603
    • (1994) Glycobiology , vol.4 , pp. 593-603
    • Reason, A.J.1    Ellis, L.A.2    Appleton, J.A.3    Wisnewski, N.4    Grieve, R.B.5    McNeil, M.6    Wassom, D.L.7    Morris, H.R.8    Dell, A.9
  • 224
    • 0031002985 scopus 로고    scopus 로고
    • Terminal beta-linked tyvelose creates unique epitopes in Trichinella spiralis glycan antigens
    • Ellis L.A., McVay C.S., Probert M.A., Zhang J., Bundle D.R., and Appleton J.A. Terminal beta-linked tyvelose creates unique epitopes in Trichinella spiralis glycan antigens. Glycobiology 7 (1997) 383-390
    • (1997) Glycobiology , vol.7 , pp. 383-390
    • Ellis, L.A.1    McVay, C.S.2    Probert, M.A.3    Zhang, J.4    Bundle, D.R.5    Appleton, J.A.6
  • 226
    • 0020137156 scopus 로고
    • 1. Synthesis of trisaccharide glycosides for use as artificial antigens
    • 1. Synthesis of trisaccharide glycosides for use as artificial antigens. Carbohydr. Res. 103 (1982) 29-40
    • (1982) Carbohydr. Res. , vol.103 , pp. 29-40
    • Iversen, T.1    Bundle, D.R.2
  • 227
    • 0001177535 scopus 로고
    • 1H nmr analysis, and semi-empirical calculations
    • 1H nmr analysis, and semi-empirical calculations. Can. J. Chem. 63 (1985) 739-744
    • (1985) Can. J. Chem. , vol.63 , pp. 739-744
    • Birnbaum, G.I.1    Bundle, D.R.2
  • 228
    • 0030448590 scopus 로고    scopus 로고
    • Synthesis of α and β-linked tyvelose epitopes of the Trichinella spiralis glycan: 2-Acetamido-2-deoxy-3-O-(3,6-dideoxy-d-arabino-hexopyranosyl)-β-d-g alactopyranosides
    • Probert M.A., Zhang J., and Bundle D.R. Synthesis of α and β-linked tyvelose epitopes of the Trichinella spiralis glycan: 2-Acetamido-2-deoxy-3-O-(3,6-dideoxy-d-arabino-hexopyranosyl)-β-d-g alactopyranosides. Carbohydr. Res. 296 (1996) 149-170
    • (1996) Carbohydr. Res. , vol.296 , pp. 149-170
    • Probert, M.A.1    Zhang, J.2    Bundle, D.R.3
  • 229
    • 0034685716 scopus 로고    scopus 로고
    • Efficient synthesis of 3,6-dideoxy-β-d-arabino-hexopyranosyl-terminated LacdiNac glycan chains of the Trichinella spiralis parasite
    • Nitz M., and Bundle D.R. Efficient synthesis of 3,6-dideoxy-β-d-arabino-hexopyranosyl-terminated LacdiNac glycan chains of the Trichinella spiralis parasite. J. Org. Chem. 65 (2000) 3064-3073
    • (2000) J. Org. Chem. , vol.65 , pp. 3064-3073
    • Nitz, M.1    Bundle, D.R.2
  • 230
    • 0001111673 scopus 로고
    • Conversion of hydroxyl groups into bromo groups in carbohydrates with inversion of configuration
    • Classon B., Garegg P.J., and Samuelson B. Conversion of hydroxyl groups into bromo groups in carbohydrates with inversion of configuration. Can. J. Chem. 59 (1981) 339-343
    • (1981) Can. J. Chem. , vol.59 , pp. 339-343
    • Classon, B.1    Garegg, P.J.2    Samuelson, B.3
  • 232
    • 0028539224 scopus 로고
    • Structure of O-specific polysaccharide chain of the Yersinia bercoviery O:10 lipopolysaccharide
    • Gorshkova R.P., Zubkov V.V., and Ovodov Yu.S. Structure of O-specific polysaccharide chain of the Yersinia bercoviery O:10 lipopolysaccharide. Bioorg. Khim. 20 (1994) 1231-1235
    • (1994) Bioorg. Khim. , vol.20 , pp. 1231-1235
    • Gorshkova, R.P.1    Zubkov, V.V.2    Ovodov, Yu.S.3
  • 233
    • 0026600185 scopus 로고
    • The branched-chain octose yersiniose A is a lipopolysaccharide constituent of Legionella micdadei and Legionella maceachernii
    • Sonesson A., and Jantzen E. The branched-chain octose yersiniose A is a lipopolysaccharide constituent of Legionella micdadei and Legionella maceachernii. J. Microbiol. Methods 15 (1992) 241-248
    • (1992) J. Microbiol. Methods , vol.15 , pp. 241-248
    • Sonesson, A.1    Jantzen, E.2
  • 235
    • 0032545041 scopus 로고    scopus 로고
    • Biosynthesis of yersiniose: Attachment of the two-carbon branched-chain is catalyzed by a thiamine pyrophosphate-dependent flavoprotein
    • Chen H., Guo Z., and Liu H.-w. Biosynthesis of yersiniose: Attachment of the two-carbon branched-chain is catalyzed by a thiamine pyrophosphate-dependent flavoprotein. J. Am. Chem. Soc. 120 (1998) 11796-11797
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 11796-11797
    • Chen, H.1    Guo, Z.2    Liu, H.-w.3
  • 236
    • 0035812679 scopus 로고    scopus 로고
    • Synthesis of a deoxysugar dinucleotide containing an exo-difluoromethylene moiety as a mechanistic probe for studying enzymes involved in unusual sugar biosynthesis
    • Zhao Z., and Liu H.-w. Synthesis of a deoxysugar dinucleotide containing an exo-difluoromethylene moiety as a mechanistic probe for studying enzymes involved in unusual sugar biosynthesis. J. Org. Chem. 66 (2001) 6810-6815
    • (2001) J. Org. Chem. , vol.66 , pp. 6810-6815
    • Zhao, Z.1    Liu, H.-w.2
  • 237
    • 5444249226 scopus 로고    scopus 로고
    • Chalcomycin biosynthesis gene cluster from Streptomyces bikiniensis: Novel features of an unusual ketolide produced through expression of the chm polyketide synthase in Streptomyces fradiae
    • and references therein
    • Ward S.L., Hu Z., Schirmer A., Reid R., Revill W.P., Reeves C.D., Petrakovsky O.V., Dong S.D., and Katz L. Chalcomycin biosynthesis gene cluster from Streptomyces bikiniensis: Novel features of an unusual ketolide produced through expression of the chm polyketide synthase in Streptomyces fradiae. Antimicrob. Agents Chemother. 48 (2004) 4703-4712 and references therein
    • (2004) Antimicrob. Agents Chemother. , vol.48 , pp. 4703-4712
    • Ward, S.L.1    Hu, Z.2    Schirmer, A.3    Reid, R.4    Revill, W.P.5    Reeves, C.D.6    Petrakovsky, O.V.7    Dong, S.D.8    Katz, L.9
  • 238
    • 0014582958 scopus 로고
    • Studies on the antibiotics from Streptomyces spinichromogenes var. kujimyceticus. II. Isolation and characterization of kujimycins A and B
    • Omura S., Namiki S., Shibata M., Muro T., and Nakayoshi H. Studies on the antibiotics from Streptomyces spinichromogenes var. kujimyceticus. II. Isolation and characterization of kujimycins A and B. J. Antibiot. 22 (1969) 500-505
    • (1969) J. Antibiot. , vol.22 , pp. 500-505
    • Omura, S.1    Namiki, S.2    Shibata, M.3    Muro, T.4    Nakayoshi, H.5
  • 239
    • 0141454893 scopus 로고    scopus 로고
    • Purification, structure determination, and antimicrobial activity of neutramycins B-G
    • Graziani E..I., Overk C.R., and Carter G.T. Purification, structure determination, and antimicrobial activity of neutramycins B-G. J. Nat. Prod. 66 (2003) 1149-1153
    • (2003) J. Nat. Prod. , vol.66 , pp. 1149-1153
    • Graziani, E..I.1    Overk, C.R.2    Carter, G.T.3
  • 240
    • 0026629738 scopus 로고
    • Biosynthesis of the erythromycin macrolactone and a rational approach for producing hybrid macrolides
    • Donadio S., Staver M.J., McAlpine J.B., Swanson S.J., and Katz L. Biosynthesis of the erythromycin macrolactone and a rational approach for producing hybrid macrolides. Gene 115 (1992) 97-103
    • (1992) Gene , vol.115 , pp. 97-103
    • Donadio, S.1    Staver, M.J.2    McAlpine, J.B.3    Swanson, S.J.4    Katz, L.5
  • 241
    • 0001749819 scopus 로고
    • Synthesis and carbon-13 n.m.r.-spectral study of methyl 2,6- and 3,6-dideoxy-α-l-arabino- and methyl 4,6-dideoxy-α-l-lyxo-hexopyranoside
    • Pozsgay V., and Neszmélyi A. Synthesis and carbon-13 n.m.r.-spectral study of methyl 2,6- and 3,6-dideoxy-α-l-arabino- and methyl 4,6-dideoxy-α-l-lyxo-hexopyranoside. Carbohydr. Res. 85 (1980) 143-150
    • (1980) Carbohydr. Res. , vol.85 , pp. 143-150
    • Pozsgay, V.1    Neszmélyi, A.2
  • 242
    • 0032735216 scopus 로고    scopus 로고
    • Syntheses of methyl (4,6-dideoxy-α-l-lyxo-hexopyranosyl)-(1→3)- and (4-deoxy-4-fluoro-α-l-rhamnopyranosyl)-(1→3)-2-acetamido-2-de oxy-α-d-glucopyranosides, analogs of the mycobacterial arabinogalactan linkage disaccharide
    • Hultin P.G., and Buffie R.M. Syntheses of methyl (4,6-dideoxy-α-l-lyxo-hexopyranosyl)-(1→3)- and (4-deoxy-4-fluoro-α-l-rhamnopyranosyl)-(1→3)-2-acetamido-2-de oxy-α-d-glucopyranosides, analogs of the mycobacterial arabinogalactan linkage disaccharide. Carbohydr. Res. 322 (1999) 14-25
    • (1999) Carbohydr. Res. , vol.322 , pp. 14-25
    • Hultin, P.G.1    Buffie, R.M.2
  • 244
    • 0014464176 scopus 로고
    • Substitution sekundärer Tosylestergruppen durch Jod Synthese von 4-Desoxy- und 4,6-Didesoxy-d-xylo-hexose
    • Siewert G., and Wastphal O. Substitution sekundärer Tosylestergruppen durch Jod Synthese von 4-Desoxy- und 4,6-Didesoxy-d-xylo-hexose. Liebigs Ann. Chem. 720 (1968) 161-170
    • (1968) Liebigs Ann. Chem. , vol.720 , pp. 161-170
    • Siewert, G.1    Wastphal, O.2
  • 245
    • 0005200721 scopus 로고
    • A facile synthesis of 4,6-dideoxy-d-xylo-hexose
    • Lawton B.T., Szarek W.A., and Jones J.K.N. A facile synthesis of 4,6-dideoxy-d-xylo-hexose. Carbohydr. Res. 14 (1970) 255-258
    • (1970) Carbohydr. Res. , vol.14 , pp. 255-258
    • Lawton, B.T.1    Szarek, W.A.2    Jones, J.K.N.3
  • 246
    • 38249033952 scopus 로고
    • Synthesis of 4,6-diedoxy-d- and -l-hexoses from racemic and meso-dipropenylglycol
    • Küfner U., and Schmidt R.R. Synthesis of 4,6-diedoxy-d- and -l-hexoses from racemic and meso-dipropenylglycol. Carbohydr. Res. 161 (1987) 211-223
    • (1987) Carbohydr. Res. , vol.161 , pp. 211-223
    • Küfner, U.1    Schmidt, R.R.2
  • 247
    • 0038647045 scopus 로고
    • Synthese von β-Glycosiden und β-Glycosidisch Verknüpften Disacchariden der d-Chalcose. Anwendung der Entchlorierung mit Tributylzinnhydrid
    • Redlich H., and Roy W. Synthese von β-Glycosiden und β-Glycosidisch Verknüpften Disacchariden der d-Chalcose. Anwendung der Entchlorierung mit Tributylzinnhydrid. Carbohydr. Res. 68 (1979) 275-285
    • (1979) Carbohydr. Res. , vol.68 , pp. 275-285
    • Redlich, H.1    Roy, W.2
  • 248
    • 0000974644 scopus 로고
    • A simple synthesis of dl-chalcose
    • Danishefsky S., and Kerwin Jr. J.F. A simple synthesis of dl-chalcose. J. Org. Chem. 47 (1982) 1597-1598
    • (1982) J. Org. Chem. , vol.47 , pp. 1597-1598
    • Danishefsky, S.1    Kerwin Jr., J.F.2
  • 249
    • 0022605744 scopus 로고
    • Synthesis of deoxyhexoses from divinylglycols. The synthesis of d- and l-chalcose
    • Küfner U., and Smidt R.R. Synthesis of deoxyhexoses from divinylglycols. The synthesis of d- and l-chalcose. Angew. Chem. Int. Ed. 25 (1986) 89
    • (1986) Angew. Chem. Int. Ed. , vol.25 , pp. 89
    • Küfner, U.1    Smidt, R.R.2
  • 250
    • 0343658306 scopus 로고
    • Synthesis of d,l-chalcose and d,l-chalcosamine
    • Torsell K., and Tyagi M.P. Synthesis of d,l-chalcose and d,l-chalcosamine. Acta Chem. Scand. B 31 (1977) 7-10
    • (1977) Acta Chem. Scand. B , vol.31 , pp. 7-10
    • Torsell, K.1    Tyagi, M.P.2
  • 251
    • 0016608564 scopus 로고
    • Synthesis of 4,6-dideoxy-d-arabino-hexose, 3,4,6-trideoxy-d-erythro- and threo-hexoses, 2,4,6-trideoxy-d-erythro-hexose, and their derivatives
    • Kefurt K., Kefurtová Z., and Jarỳ J. Synthesis of 4,6-dideoxy-d-arabino-hexose, 3,4,6-trideoxy-d-erythro- and threo-hexoses, 2,4,6-trideoxy-d-erythro-hexose, and their derivatives. Collect. Czechoslov. Chem. Commun. 40 (1975) 164-173
    • (1975) Collect. Czechoslov. Chem. Commun. , vol.40 , pp. 164-173
    • Kefurt, K.1    Kefurtová, Z.2    Jarỳ, J.3
  • 252
    • 0035798211 scopus 로고    scopus 로고
    • Synthesis of 4,6-dideoxyfuranoses through the regioselective and diastereoselective oxyfunctionalization of a dimethylphenylsilyl-substituted chiral homoallylic alcohol
    • Adam W., Saha-Moller C.R., and Schmid K.S. Synthesis of 4,6-dideoxyfuranoses through the regioselective and diastereoselective oxyfunctionalization of a dimethylphenylsilyl-substituted chiral homoallylic alcohol. J. Org. Chem. 66 (2001) 7365-7371
    • (2001) J. Org. Chem. , vol.66 , pp. 7365-7371
    • Adam, W.1    Saha-Moller, C.R.2    Schmid, K.S.3
  • 253
    • 27144456831 scopus 로고    scopus 로고
    • Electrooxidative glycosylation through C-S bond cleavage of 1-arylthio-2,3-dideoxyglycosides. Synthesis of 2′,3′-dideoxynucleosides
    • Mitsudo K., Kawaguchi T., Miyahara S., Matsuda W., Kuroboshi M., and Tanaka H. Electrooxidative glycosylation through C-S bond cleavage of 1-arylthio-2,3-dideoxyglycosides. Synthesis of 2′,3′-dideoxynucleosides. Org. Lett. 7 (2005) 4649-4652
    • (2005) Org. Lett. , vol.7 , pp. 4649-4652
    • Mitsudo, K.1    Kawaguchi, T.2    Miyahara, S.3    Matsuda, W.4    Kuroboshi, M.5    Tanaka, H.6
  • 254
    • 0037118313 scopus 로고    scopus 로고
    • Enantioselective synthesis of 2-deoxy- and 2,3-dideoxyhexoses
    • Haukaas M.H., and O'Doherty G.A. Enantioselective synthesis of 2-deoxy- and 2,3-dideoxyhexoses. Org. Lett. 4 (2002) 1771-1774
    • (2002) Org. Lett. , vol.4 , pp. 1771-1774
    • Haukaas, M.H.1    O'Doherty, G.A.2
  • 255
    • 0021762866 scopus 로고
    • Synthesis of 2,4-dideoxy-d-erythro-hexopyranose. An intermediate for synthesis of the lactone moiety of inhibitors of hydroxymethylglutaryl-coenzyme A reductase
    • Ho P.-T., and Chung S. Synthesis of 2,4-dideoxy-d-erythro-hexopyranose. An intermediate for synthesis of the lactone moiety of inhibitors of hydroxymethylglutaryl-coenzyme A reductase. Carbohydr. Res. 125 (1984) 318-322
    • (1984) Carbohydr. Res. , vol.125 , pp. 318-322
    • Ho, P.-T.1    Chung, S.2
  • 257
    • 0026479041 scopus 로고
    • Synthesis of 1-(2,4-dideoxy-β-d-erythro-hexopyranosyl)thymine and its incorporation into oligonucleotides
    • Augustyns K., Van Aerschot A., and Herdwijn P. Synthesis of 1-(2,4-dideoxy-β-d-erythro-hexopyranosyl)thymine and its incorporation into oligonucleotides. Bioorg. Med. Chem. Lett. 2 (1992) 945-948
    • (1992) Bioorg. Med. Chem. Lett. , vol.2 , pp. 945-948
    • Augustyns, K.1    Van Aerschot, A.2    Herdwijn, P.3
  • 258
    • 0034784153 scopus 로고    scopus 로고
    • Modeling of deoxy- and dideoxyaldohexopyranosyl ring puckering with MM3(92)
    • Rockey W.M., Dowd M.K., Reilly P.J., and French A.D. Modeling of deoxy- and dideoxyaldohexopyranosyl ring puckering with MM3(92). Carbohydr. Res. 335 (2001) 261-273
    • (2001) Carbohydr. Res. , vol.335 , pp. 261-273
    • Rockey, W.M.1    Dowd, M.K.2    Reilly, P.J.3    French, A.D.4
  • 262
    • 0027057232 scopus 로고
    • Dutomycin, a new anthracycline antibiotic from Streptomyces
    • Xuan L., Xu S., Zhang H., Xu Y., and Chen M. Dutomycin, a new anthracycline antibiotic from Streptomyces. J. Antibiot. 45 (1992) 1974-1976
    • (1992) J. Antibiot. , vol.45 , pp. 1974-1976
    • Xuan, L.1    Xu, S.2    Zhang, H.3    Xu, Y.4    Chen, M.5
  • 263
    • 0031913370 scopus 로고    scopus 로고
    • Polyketomycin, a new antibiotic from Streptomyces sp. MK277-AF1. II. Structure determination
    • Momose I., Chen W., Nakamura H., Naganawa H., Inuma H., and Takeuchi T. Polyketomycin, a new antibiotic from Streptomyces sp. MK277-AF1. II. Structure determination. J. Antibiot. 51 (1998) 26-32
    • (1998) J. Antibiot. , vol.51 , pp. 26-32
    • Momose, I.1    Chen, W.2    Nakamura, H.3    Naganawa, H.4    Inuma, H.5    Takeuchi, T.6
  • 266
    • 0031888991 scopus 로고    scopus 로고
    • Polyketomycin, a new antibiotic from Streptomyces sp. MK277-AF1. I. Taxonomy, production, isolation, physico-chemical properties and biological activities
    • Momose I., Chen W., Kinoshita N., Iinuma H., Hamada M., and Takeuchi T. Polyketomycin, a new antibiotic from Streptomyces sp. MK277-AF1. I. Taxonomy, production, isolation, physico-chemical properties and biological activities. J. Antibiot. 51 (1998) 21-25
    • (1998) J. Antibiot. , vol.51 , pp. 21-25
    • Momose, I.1    Chen, W.2    Kinoshita, N.3    Iinuma, H.4    Hamada, M.5    Takeuchi, T.6
  • 268
    • 7844247172 scopus 로고
    • Zur Kenntnis der β-Rhodomycine
    • Brockman H., and Greve H. Zur Kenntnis der β-Rhodomycine. Tetrahedron Lett. 16 (1975) 831-834
    • (1975) Tetrahedron Lett. , vol.16 , pp. 831-834
    • Brockman, H.1    Greve, H.2
  • 269
    • 0041848591 scopus 로고    scopus 로고
    • Characterization of mutations in aclacinomycin A-non-producing Stretomyces galilaeus strains with altered glycosylation patterns
    • and references therein
    • Räty K., Hautala A., Torkkell S., Kantola J., Mäntsälä P., Hakala J., and Ylihonko K. Characterization of mutations in aclacinomycin A-non-producing Stretomyces galilaeus strains with altered glycosylation patterns. Microbiology 148 (2002) 3375-3384 and references therein
    • (2002) Microbiology , vol.148 , pp. 3375-3384
    • Räty, K.1    Hautala, A.2    Torkkell, S.3    Kantola, J.4    Mäntsälä, P.5    Hakala, J.6    Ylihonko, K.7
  • 270
    • 0345543876 scopus 로고
    • Stereochemical identification and synthesis of amicetose and the stereochemical identification of rhodinose and the sugar from Streptolydigin
    • Stevens C.L., Blumbergs P., and Wood D.L. Stereochemical identification and synthesis of amicetose and the stereochemical identification of rhodinose and the sugar from Streptolydigin. J. Am. Chem. Soc. 86 (1964) 3592
    • (1964) J. Am. Chem. Soc. , vol.86 , pp. 3592
    • Stevens, C.L.1    Blumbergs, P.2    Wood, D.L.3
  • 271
    • 0000616941 scopus 로고
    • Synthesis of methyl 2,3,6-trideoxy-α-d-erythro-hexopyranoside (methyl α-amicetoside)
    • Albano E.L., and Horton D. Synthesis of methyl 2,3,6-trideoxy-α-d-erythro-hexopyranoside (methyl α-amicetoside). J. Org. Chem. 34 (1969) 3519-3522
    • (1969) J. Org. Chem. , vol.34 , pp. 3519-3522
    • Albano, E.L.1    Horton, D.2
  • 272
    • 0015537211 scopus 로고
    • The relayed introduction of alkylthio-groups into carbohydrates derivatives: A novel synthesis of amicetose
    • Bethell G.S., and Ferrier R.J. The relayed introduction of alkylthio-groups into carbohydrates derivatives: A novel synthesis of amicetose. J. Chem. Soc. Perkin I (1993) 1400-1405
    • (1993) J. Chem. Soc. Perkin I , pp. 1400-1405
    • Bethell, G.S.1    Ferrier, R.J.2
  • 273
    • 0015449611 scopus 로고
    • Syntheses of methyl 2,3,6-trideoxy-α-l-erythro-hexopyranoside (methyl α-l-hexopyranoside) and methyl 2,3,4,6-tetradeoxy-4-(dimethylamino)-α-l-threo-hexopyranoside
    • Brimacombe J.S., Doner L.W., and Rollins A.J. Syntheses of methyl 2,3,6-trideoxy-α-l-erythro-hexopyranoside (methyl α-l-hexopyranoside) and methyl 2,3,4,6-tetradeoxy-4-(dimethylamino)-α-l-threo-hexopyranoside. J. Chem. Soc. Perkin I (1972) 2977-2979
    • (1972) J. Chem. Soc. Perkin I , pp. 2977-2979
    • Brimacombe, J.S.1    Doner, L.W.2    Rollins, A.J.3
  • 274
    • 0000033757 scopus 로고
    • Synthesis of d-amicetose and l-rhodinose from l-glutamic acid
    • Berti G., Caroti P., Catelani G., and Monti L. Synthesis of d-amicetose and l-rhodinose from l-glutamic acid. Carbohydr. Res. 124 (1983) 35-42
    • (1983) Carbohydr. Res. , vol.124 , pp. 35-42
    • Berti, G.1    Caroti, P.2    Catelani, G.3    Monti, L.4
  • 277
    • 0002867379 scopus 로고
    • The synthesis of trideoxy sugars. A preparation of rhodinose (2,3,6-trideoxy-α-l-threo-hexose) and methyl 2,3,6-trideoxy-α-l-erythro-hexopyranoside
    • Haines A.H. The synthesis of trideoxy sugars. A preparation of rhodinose (2,3,6-trideoxy-α-l-threo-hexose) and methyl 2,3,6-trideoxy-α-l-erythro-hexopyranoside. Carbohydr. Res. 21 (1972) 99-109
    • (1972) Carbohydr. Res. , vol.21 , pp. 99-109
    • Haines, A.H.1
  • 278
    • 33947483562 scopus 로고
    • A new, stereospecific olefin synthesis from 1,2-diols
    • Corey E.J., and Winter R.A.E. A new, stereospecific olefin synthesis from 1,2-diols. J. Am. Chem. Soc. 85 (1963) 2677-2678
    • (1963) J. Am. Chem. Soc. , vol.85 , pp. 2677-2678
    • Corey, E.J.1    Winter, R.A.E.2
  • 279
    • 0001466383 scopus 로고
    • Rhodinose derivatives suitable for the synthesis of anthracycline analogs
    • El Khadem H.E., and Cermak R.C. Rhodinose derivatives suitable for the synthesis of anthracycline analogs. Carbohydr. Res. 75 (1979) 335-339
    • (1979) Carbohydr. Res. , vol.75 , pp. 335-339
    • El Khadem, H.E.1    Cermak, R.C.2
  • 280
    • 0001006163 scopus 로고
    • A simple synthesis of rhodinose from (S)-ethyl lactate
    • Ross Kelly T., and Kaul P.N. A simple synthesis of rhodinose from (S)-ethyl lactate. J. Org. Chem. 48 (1983) 2775-2777
    • (1983) J. Org. Chem. , vol.48 , pp. 2775-2777
    • Ross Kelly, T.1    Kaul, P.N.2
  • 281
    • 0000845355 scopus 로고
    • 2,2,5-Trimethyl-1,3-dioxolane-4-carboxaldehyde as a chiral synthon: Synthesis of the two enantiomers of methyl 2,3,6-trideoxy-α-l-threo-hex-2-enopyranoside, key intermediate in the synthesis of daunosamine and of (+)- and (-)-rhodinose
    • Servi S. 2,2,5-Trimethyl-1,3-dioxolane-4-carboxaldehyde as a chiral synthon: Synthesis of the two enantiomers of methyl 2,3,6-trideoxy-α-l-threo-hex-2-enopyranoside, key intermediate in the synthesis of daunosamine and of (+)- and (-)-rhodinose. J. Org. Chem. 50 (1985) 5865-5867
    • (1985) J. Org. Chem. , vol.50 , pp. 5865-5867
    • Servi, S.1
  • 282
    • 0028893527 scopus 로고
    • Synthesis of specifically labelled 2,3,6-trideoxyhexoses
    • Kirschning A., Hary U., and Ries M. Synthesis of specifically labelled 2,3,6-trideoxyhexoses. Tetrahedron 51 (1995) 2297-2304
    • (1995) Tetrahedron , vol.51 , pp. 2297-2304
    • Kirschning, A.1    Hary, U.2    Ries, M.3
  • 283
    • 0016608564 scopus 로고
    • Synthesis of 4,6-dideoxy-d-arabino-hexose, 3,4,6-trideoxy-d-erythro- and threo-hexoses, 2,4,6-trideoxy-d-erythro-hexose, and their derivatives
    • Kefurt K., Kefurtová Z., and Jarý J. Synthesis of 4,6-dideoxy-d-arabino-hexose, 3,4,6-trideoxy-d-erythro- and threo-hexoses, 2,4,6-trideoxy-d-erythro-hexose, and their derivatives. Collect. Czechoslov. Chem. Commun. 40 (1975) 164-173
    • (1975) Collect. Czechoslov. Chem. Commun. , vol.40 , pp. 164-173
    • Kefurt, K.1    Kefurtová, Z.2    Jarý, J.3
  • 284
    • 0006107725 scopus 로고
    • β-Elimination in aldonolactones: Synthesis of 2-O-benzoyl-3,5,6-trideoxy-α-dl-threo-hexofuranose
    • Varela O.J., Fernández Cirelli A., and de Lederkremer R.M. β-Elimination in aldonolactones: Synthesis of 2-O-benzoyl-3,5,6-trideoxy-α-dl-threo-hexofuranose. Carbohydr. Res. 100 (1982) 424-430
    • (1982) Carbohydr. Res. , vol.100 , pp. 424-430
    • Varela, O.J.1    Fernández Cirelli, A.2    de Lederkremer, R.M.3
  • 285
    • 34948839593 scopus 로고
    • Síntesis de 2-O-benzoil-3,4,6-tridesoxi-dl-treo-hexopiranosa, un nuevo ejemplo de síntesis de desoxiazúcares via reacciónes de eliminación-β en aldonolactonas
    • Sznaidman M., Fernández Cirelli A., and de Lederkremer R.M. Síntesis de 2-O-benzoil-3,4,6-tridesoxi-dl-treo-hexopiranosa, un nuevo ejemplo de síntesis de desoxiazúcares via reacciónes de eliminación-β en aldonolactonas. Anales Asoc. Quím. Argentina 70 (1982) 341-348
    • (1982) Anales Asoc. Quím. Argentina , vol.70 , pp. 341-348
    • Sznaidman, M.1    Fernández Cirelli, A.2    de Lederkremer, R.M.3


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