-
2
-
-
0002334440
-
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
-
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
-
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
-
6
-
-
11144296792
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
51
-
-
0030598022
-
Reactivity of glucosyl radical in the presence of phenols
-
Alberti A., Della Bona M.A., Macciantelli D., Pelizzoni F., Sello G., Torri G., and Vismara E. Reactivity of glucosyl radical in the presence of phenols. Tetrahedron 52 (1996) 10241-10248
-
(1996)
Tetrahedron
, vol.52
, pp. 10241-10248
-
-
Alberti, A.1
Della Bona, M.A.2
Macciantelli, D.3
Pelizzoni, F.4
Sello, G.5
Torri, G.6
Vismara, E.7
-
52
-
-
0034703343
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
69
-
-
0033571254
-
Total synthesis of everninomicin 13,384-1-Part 1: Synthesis of the A(1)B(A)C fragment
-
Nicolaou K.C., Mitchell H.J., Suzuki H., Rodriguez R.H., Bauoin O., and Fylaktakidou K.C. Total synthesis of everninomicin 13,384-1-Part 1: Synthesis of the A(1)B(A)C fragment. Angew. Chem. Int. Ed. Engl. 38 (1999) 3334-3339
-
(1999)
Angew. Chem. Int. Ed. Engl.
, vol.38
, pp. 3334-3339
-
-
Nicolaou, K.C.1
Mitchell, H.J.2
Suzuki, H.3
Rodriguez, R.H.4
Bauoin, O.5
Fylaktakidou, K.C.6
-
71
-
-
0025814857
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
93
-
-
0032192090
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
112
-
-
0032380009
-
Cardenolide glycosides from seeds of Corchorus olitorius
-
Nakamura T., Goda Y., Sakai S., Kondo K., Akiyama H., and Toyoda M. Cardenolide glycosides from seeds of Corchorus olitorius. Phytochemistry 49 (1998) 2097-2102
-
(1998)
Phytochemistry
, vol.49
, pp. 2097-2102
-
-
Nakamura, T.1
Goda, Y.2
Sakai, S.3
Kondo, K.4
Akiyama, H.5
Toyoda, M.6
-
113
-
-
0842306098
-
C,O-bisglycosylapigenins from the leaves of Rhamnella inaequilatera
-
Takeda Y., Okada Y., Masuda T., Hirata E., Shinzato T., and Otsuka H. C,O-bisglycosylapigenins from the leaves of Rhamnella inaequilatera. Phytochemistry 65 (2004) 463-468
-
(2004)
Phytochemistry
, vol.65
, pp. 463-468
-
-
Takeda, Y.1
Okada, Y.2
Masuda, T.3
Hirata, E.4
Shinzato, T.5
Otsuka, H.6
-
114
-
-
0038336048
-
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
-
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
-
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
-
117
-
-
0026710498
-
The confomational behaviour of the cardiac glycoside digoxin as indicated by NMR spectroscopy and molecular dynamics calculations
-
Aulabaugh A.E., Crouch R.C., Martin G.E., Ragouezeos A., Shockcor J.P., Spitzer T.D., Duncan Farrant R., Hudson B.D., and Lindon J.C. The confomational behaviour of the cardiac glycoside digoxin as indicated by NMR spectroscopy and molecular dynamics calculations. Carbohydr. Res. 230 (1992) 201-213
-
(1992)
Carbohydr. Res.
, vol.230
, pp. 201-213
-
-
Aulabaugh, A.E.1
Crouch, R.C.2
Martin, G.E.3
Ragouezeos, A.4
Shockcor, J.P.5
Spitzer, T.D.6
Duncan Farrant, R.7
Hudson, B.D.8
Lindon, J.C.9
-
118
-
-
0025895057
-
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
-
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
-
120
-
-
0035056172
-
Sweet pregnane glycosides from Telosma procumbens
-
Huan V.D., Ohtani K., Kasai R., Yamasaki K., and Tuu N.V. Sweet pregnane glycosides from Telosma procumbens. Chem. Pharm. Bull. 49 (2001) 453-460
-
(2001)
Chem. Pharm. Bull.
, vol.49
, pp. 453-460
-
-
Huan, V.D.1
Ohtani, K.2
Kasai, R.3
Yamasaki, K.4
Tuu, N.V.5
-
121
-
-
0034624465
-
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
-
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
-
123
-
-
0036692099
-
Pregnane and pregnane glycosides from the malagasy plant, Cynanchum aphyllum
-
Kanchanapoom T., Kasai R., Ohtani K., Andriantsiferana M., and Yamasaki K. Pregnane and pregnane glycosides from the malagasy plant, Cynanchum aphyllum. Chem. Pharm. Bull. 50 (2002) 1031-1034
-
(2002)
Chem. Pharm. Bull.
, vol.50
, pp. 1031-1034
-
-
Kanchanapoom, T.1
Kasai, R.2
Ohtani, K.3
Andriantsiferana, M.4
Yamasaki, K.5
-
124
-
-
0033943342
-
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
-
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
-
126
-
-
0033541151
-
Functional characterization of the jadI gene as a cyclase forming angucyclinones
-
Kulowski K., Wendt-Pienkowski E., Han L., Yang K., Vining L.C., and Hutchinson C.R. Functional characterization of the jadI gene as a cyclase forming angucyclinones. J. Am. Chem. Soc. 121 (1999) 1786-1794
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 1786-1794
-
-
Kulowski, K.1
Wendt-Pienkowski, E.2
Han, L.3
Yang, K.4
Vining, L.C.5
Hutchinson, C.R.6
-
127
-
-
1842789152
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
138
-
-
18544372619
-
Durhamycin A a potent inhibitor of HIV Tat transactivation
-
Jayasuriya H., Lingham R.B., Graham P., Quamina D., Herranz L., Genilloud O., Gagliardi M., Danzeisen R., Tomassini J.E., Zink D.L., Guan Z., and Singh S.B. Durhamycin A a potent inhibitor of HIV Tat transactivation. J. Nat. Prod. 65 (2002) 1091-1095
-
(2002)
J. Nat. Prod.
, vol.65
, pp. 1091-1095
-
-
Jayasuriya, H.1
Lingham, R.B.2
Graham, P.3
Quamina, D.4
Herranz, L.5
Genilloud, O.6
Gagliardi, M.7
Danzeisen, R.8
Tomassini, J.E.9
Zink, D.L.10
Guan, Z.11
Singh, S.B.12
-
139
-
-
0031690038
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
150
-
-
0031754801
-
Improved efficacy and enlarged spectrum of activity of a novel anthracycline disaccharide analogue of doxorubicin against human tumor xenografts
-
Pratesi G., Cesare M.E., Caserini C., Perego P., Bo L.D., Polizzi D., Supino R., Bigioni M., Manzini S., Iafrate E., Salvatore C., Casazza A., Arcamone F., and Zunino F. Improved efficacy and enlarged spectrum of activity of a novel anthracycline disaccharide analogue of doxorubicin against human tumor xenografts. Clin. Cancer Res. 4 (1998) 2833-2839
-
(1998)
Clin. Cancer Res.
, vol.4
, pp. 2833-2839
-
-
Pratesi, G.1
Cesare, M.E.2
Caserini, C.3
Perego, P.4
Bo, L.D.5
Polizzi, D.6
Supino, R.7
Bigioni, M.8
Manzini, S.9
Iafrate, E.10
Salvatore, C.11
Casazza, A.12
Arcamone, F.13
Zunino, F.14
-
151
-
-
0028060661
-
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
-
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
-
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
-
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
-
155
-
-
3142663153
-
Carbohydrates from Cynanchum otophyllum
-
Zhao Y.-B., Shen Y.-M., He H.-P., Li Y.-M., Mu Q.-Z., and Hao X.-J. Carbohydrates from Cynanchum otophyllum. Carbohydr. Res. 339 (2004) 1967-1972
-
(2004)
Carbohydr. Res.
, vol.339
, pp. 1967-1972
-
-
Zhao, Y.-B.1
Shen, Y.-M.2
He, H.-P.3
Li, Y.-M.4
Mu, Q.-Z.5
Hao, X.-J.6
-
156
-
-
0025268291
-
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
-
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
-
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
-
159
-
-
0032522214
-
Structure of apoptolidin, a specific apoptosis inducer in transformed cells
-
Hayakawa Y., Kim J.W., Adachi H., Shin-ya K., Fujita K.-i., and Seto H. Structure of apoptolidin, a specific apoptosis inducer in transformed cells. J. Am. Chem. Soc. 120 (1998) 3524-3525
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 3524-3525
-
-
Hayakawa, Y.1
Kim, J.W.2
Adachi, H.3
Shin-ya, K.4
Fujita, K.-i.5
Seto, H.6
-
160
-
-
25444462806
-
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
-
161
-
-
5344244764
-
Total synthesis of apoptolidin
-
Wehlan H., Dauber M., Mujica Fernaud M.T., Schuppan J., Mahrwald R., Ziemer B., Juarez Garciz M.E., and Koert U. Total synthesis of apoptolidin. Angew. Chem. Int. Ed. 43 (2004) 4597-4601
-
(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 4597-4601
-
-
Wehlan, H.1
Dauber, M.2
Mujica Fernaud, M.T.3
Schuppan, J.4
Mahrwald, R.5
Ziemer, B.6
Juarez Garciz, M.E.7
Koert, U.8
-
162
-
-
10744222793
-
Total synthesis of apoptolidin: Completion of the synthesis and analogue synthesis and evaluation
-
Nicolaou K.C., Li Y., Sugita K., Monenschein H., Guntupalli P., Mitchell H.J., Fylaktakidou K.C., Vourloumis D., Giannakakou P., and O'Brate A. Total synthesis of apoptolidin: Completion of the synthesis and analogue synthesis and evaluation. J. Am. Chem. Soc. 125 (2003) 15443-15454
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 15443-15454
-
-
Nicolaou, K.C.1
Li, Y.2
Sugita, K.3
Monenschein, H.4
Guntupalli, P.5
Mitchell, H.J.6
Fylaktakidou, K.C.7
Vourloumis, D.8
Giannakakou, P.9
O'Brate, A.10
-
163
-
-
0034007775
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
173
-
-
37049108468
-
Convenient synthesis of l-digitoxose, l-cymarose, and l-ristosamine
-
Brimacombe J.S., Hann R., Saeed M.S., and Tucker L.C.N. Convenient synthesis of l-digitoxose, l-cymarose, and l-ristosamine. J. Chem. Soc. Perkin I 1 (1982) 2583-2587
-
(1982)
J. Chem. Soc. Perkin I
, vol.1
, pp. 2583-2587
-
-
Brimacombe, J.S.1
Hann, R.2
Saeed, M.S.3
Tucker, L.C.N.4
-
174
-
-
34948838030
-
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
-
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
-
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
-
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
-
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
-
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
-
180
-
-
19944426975
-
Synthesis, surface active and antimicrobial properties of new alkyl 2,6-dideoxy-l-arabino-hexopyranosides
-
Rauter A.P., Lucas S., Almeida T., Sacoto D., Ribeiro V., Justino J., Neves A., Silva F.V., Oliveira M.C., Ferreira M.J., Santos M.S., and Barbosa E. Synthesis, surface active and antimicrobial properties of new alkyl 2,6-dideoxy-l-arabino-hexopyranosides. Carbohydr. Res. 340 (2005) 191-201
-
(2005)
Carbohydr. Res.
, vol.340
, pp. 191-201
-
-
Rauter, A.P.1
Lucas, S.2
Almeida, T.3
Sacoto, D.4
Ribeiro, V.5
Justino, J.6
Neves, A.7
Silva, F.V.8
Oliveira, M.C.9
Ferreira, M.J.10
Santos, M.S.11
Barbosa, E.12
-
181
-
-
0034856716
-
(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
-
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
202
-
-
0028279360
-
Molecular recognition of a Salmonella trisaccharide epitope by monoclonal antibody Se155-4
-
Bundle D.R., Eichler E., Gidney M.A., Meldal M., Ragauskas A., Sigurskjold B.W., Sinnott B., Watson D.C., Yaguchi M., and Young N.M. Molecular recognition of a Salmonella trisaccharide epitope by monoclonal antibody Se155-4. Biochemistry 33 (1994) 5172-5182
-
(1994)
Biochemistry
, vol.33
, pp. 5172-5182
-
-
Bundle, D.R.1
Eichler, E.2
Gidney, M.A.3
Meldal, M.4
Ragauskas, A.5
Sigurskjold, B.W.6
Sinnott, B.7
Watson, D.C.8
Yaguchi, M.9
Young, N.M.10
-
204
-
-
0025707962
-
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
-
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
-
206
-
-
0034635621
-
A practical route to 3,6-dideoxyhexoses
-
Yu H.N., Zhang P., Ling C.-C., and Bundle D.R. A practical route to 3,6-dideoxyhexoses. Tetrahedron Asymmetry 11 (2000) 465-479
-
(2000)
Tetrahedron Asymmetry
, vol.11
, pp. 465-479
-
-
Yu, H.N.1
Zhang, P.2
Ling, C.-C.3
Bundle, D.R.4
-
208
-
-
0000455282
-
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
-
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
-
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
-
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
-
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
-
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
-
214
-
-
0035933552
-
T
-
T. Carbohydr. Res. 333 (2001) 41-46
-
(2001)
Carbohydr. Res.
, vol.333
, pp. 41-46
-
-
Muldoon, J.1
Perepelov, A.V.2
Shashkov, A.S.3
Gorshkova, R.P.4
Nazarenko, E.L.5
Zubkov, V.A.6
Ivanova, E.P.7
Knirel, Y.A.8
Savage, A.V.9
-
215
-
-
0029155854
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
225
-
-
4644257767
-
Evaluation of Trichinella spiralis larva group 1 antigens for serodiagnosis of human trichinellosis
-
Escalante M., Romaris F., Rodriguez M., Rodriguez E., Leiro J., Garate M.T., and Ubeira F.M. Evaluation of Trichinella spiralis larva group 1 antigens for serodiagnosis of human trichinellosis. J. Clin. Microbiol. 42 (2004) 4060-4066
-
(2004)
J. Clin. Microbiol.
, vol.42
, pp. 4060-4066
-
-
Escalante, M.1
Romaris, F.2
Rodriguez, M.3
Rodriguez, E.4
Leiro, J.5
Garate, M.T.6
Ubeira, F.M.7
-
226
-
-
0020137156
-
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
-
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
-
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
-
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
-
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
-
231
-
-
0021763042
-
Yersiniose, a new branched-chain sugar
-
Gorshkova R.P., Zubkov V.A., V: Isakov V., and Ovodov Y.S. Yersiniose, a new branched-chain sugar. Carbohydr. Res. 126 (1984) 308-312
-
(1984)
Carbohydr. Res.
, vol.126
, pp. 308-312
-
-
Gorshkova, R.P.1
Zubkov, V.A.2
Isakov, V.3
Ovodov, Y.S.4
-
232
-
-
0028539224
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
243
-
-
0030053683
-
Synthesis of the 4-, 6-deoxy, and 4,6-dideoxy derivatives of d-mannose
-
Nishio T., Miyake Y., Kubota K., Yamai M., Miki S., Ito T., and Oku T. Synthesis of the 4-, 6-deoxy, and 4,6-dideoxy derivatives of d-mannose. Carbohydr. Res. 280 (1996) 357-363
-
(1996)
Carbohydr. Res.
, vol.280
, pp. 357-363
-
-
Nishio, T.1
Miyake, Y.2
Kubota, K.3
Yamai, M.4
Miki, S.5
Ito, T.6
Oku, T.7
-
244
-
-
0014464176
-
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
-
246
-
-
38249033952
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
256
-
-
0015505875
-
Total syntheses of negamycin and the antipode
-
Shibahara S., Kondo S., Maeda K., Umezawa H., and Ohno M. Total syntheses of negamycin and the antipode. J. Am. Chem. Soc. 94 (1972) 4353-4354
-
(1972)
J. Am. Chem. Soc.
, vol.94
, pp. 4353-4354
-
-
Shibahara, S.1
Kondo, S.2
Maeda, K.3
Umezawa, H.4
Ohno, M.5
-
257
-
-
0026479041
-
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
-
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
-
260
-
-
0015931628
-
Axenomycin. I. The structure of chromophore and sugar moieties
-
Arcamone F., Barbieri W., Franceschi G., Penco S., and Vigevani A. Axenomycin. I. The structure of chromophore and sugar moieties. J. Am. Chem. Soc. 95 (1973) 2008-2009
-
(1973)
J. Am. Chem. Soc.
, vol.95
, pp. 2008-2009
-
-
Arcamone, F.1
Barbieri, W.2
Franceschi, G.3
Penco, S.4
Vigevani, A.5
-
261
-
-
0015931648
-
Axenomycins. II. The structure of axenolide
-
Arcamone F., Franceschi G., Gioia B., Penco S., and Vigevani A. Axenomycins. II. The structure of axenolide. J. Am. Chem. Soc. 95 (1973) 2009-2011
-
(1973)
J. Am. Chem. Soc.
, vol.95
, pp. 2009-2011
-
-
Arcamone, F.1
Franceschi, G.2
Gioia, B.3
Penco, S.4
Vigevani, A.5
-
262
-
-
0027057232
-
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
-
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
-
265
-
-
1642359191
-
Synthesis of the polyketomycin disaccharide
-
Micalizzi D.S., Dougherty J.P., Noecker L.A., Smith G.R., and Giuliano R.M. Synthesis of the polyketomycin disaccharide. Tetrahedron Asymmetry 14 (2003) 3183-3188
-
(2003)
Tetrahedron Asymmetry
, vol.14
, pp. 3183-3188
-
-
Micalizzi, D.S.1
Dougherty, J.P.2
Noecker, L.A.3
Smith, G.R.4
Giuliano, R.M.5
-
266
-
-
0031888991
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
276
-
-
0032579307
-
Synthesis of amicetose by three enentioselective methods
-
and references therein
-
Noecker L.A., Martino J.A., Foley P.J., Rush D.M., Giuliano R.M., and Villani Jr. F.J. Synthesis of amicetose by three enentioselective methods. Tetrahedron Asymmetry 9 (1998) 203-212 and references therein
-
(1998)
Tetrahedron Asymmetry
, vol.9
, pp. 203-212
-
-
Noecker, L.A.1
Martino, J.A.2
Foley, P.J.3
Rush, D.M.4
Giuliano, R.M.5
Villani Jr., F.J.6
-
277
-
-
0002867379
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
|