An easy-to-use reference resource for all scientists operating with carbohydrates, the Dictionary of Carbohydrates with CD-ROM, moment version builds at the good fortune of its past version through offering a considerably elevated variety of compounds. The presentation is sharpened via a cautious overview of latest entries. With 24,000 compounds, it represents a far enlarged and revised new version of the dictionary first released in 1998. every one access includes a wealth of data together with: names and synonyms, molecular formulae, chemical buildings, exact mass, UV spectra, large resource facts, actual houses, makes use of and key literature citations.
The re-creation of this authoritative reference contains a structure-searchable CD-ROM that gives fast, handy entry to crucial info. the mix of 33 searchable textual content fields and whole substructure looking out power offers the carbohydrate chemist with the instruments to immediately seek the total database for the proper details. seek effects could be seen on monitor, published or kept. this mixture of publication and CD can provide much more entry to the data you wish each day.
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Et al. , J. O. C. , 1970, 35, 464 (synth, D-form) Israel, M. et al. , J. Het. Chem. , 1973, 10, 209 (synth, L-form) Tronchet, J. M. J. et al. , Carbohydr. Res. , 1975, forty two, 347 (diisopropylidene, pmr, ms) Bognar, R. et al. , Org. Prep. Proced. Int. , 1975, 7, 111 (N-Ph N-Me) Blanc-Muesser, M. et al. , Carbohydr. Res. , 1979, sixty eight, one hundred seventy five (synth, D-form, pmr) Andrews, M. A. et al. , J. O. C. , 1989, fifty four, 5257 (N-Ac) 4-Amino-4-deoxyarabinitol 2-Amino-2-deoxyarabinitol NH 2 A-176 A-175 CH 2OH HO OH NH 2 CH 2OH C5H13NO4 151. 162 The identify 4-amino-4-deoxyarabinitol has priority acc.
A]20 D -23. 1 (c, 1 in CHCl3). 3-Benzyl: 1,5-Anhydro-3-O-benzyl-b-Dxylofuranose, 9CI. 1,4-Anhydro-3-Obenzyl-a-D-xylopyranose [213963-76-9] C12H14O4 222. 24 Yellow syrup. [a]25 D -7. sixty four (c, 1 in CHCl3). D-form 3-Benzyl, 2-Ac: 2-O-Acetyl-1,5-anhydro-3O-benzyl-b-D-xylofuranose, 9CI. 2-OAcetyl-1,4-anhydro-3-O-benzyl-a-Dxylopyranose [213963-73-6] C14H16O5 264. 277 Yellow oil. [a]21 D -43. nine (c, 1 in CHCl3). 3-Benzyl, 2-pivaloyl: 1,5-Anhydro-3-Obenzyl-2-O-pivaloyl-b-D-xylofuranose. 1,4-Anhydro-3-O-benzyl-2-O-pivaloyl-aD-xylopyranose [213963-72-5] C17H22O5 306.
A. et al. , Carbohydr. Res. , 1984, 132, fifty one (synth, deriv) A-460 3-Amino-2,3,6-trideoxy-lyxo hexose A-461 Daunosamine CH three O HO NH 2 α−D−Pyranose−form OH C6H13NO3 147. 174 D-form Hydrolysis prod. of Daunomycin. N-Ac: 3-Acetamido-2,3,6-trideoxy-D-lyxohexose [23089-62-5] C8H15NO4 189. 211 Cryst. (EtOAc). Mp 145-1468. [a]23 D +101 zero/ +94. 2 (c, zero. five in H2O). N-Benzoyl: 3-Benzamido-2,3,6-trideoxy-Dlyxo-hexose C13H17NO4 251. 282 Mp 1518. [a]D +110. five (EtOH). a-D-Pyranose-form Me glycoside, 3,4-di-Ac: Methyl 3-acetamido-4-O-acetyl-2,3,6-trideoxy-a-Dlyxo-hexopyranoside [6605-26-1] C11H19NO5 245.
A]D 20 (c, zero. 33 in MeOH). 2,3,4,6-Tetrabenzyl: 2,3,4,6-Tetra-O-benzyl-L-altrose [222416-57-1] C34H36O6 540. 655 [a]24 D +8. sixty four (c, 1. 1 in CHCl3). L-form HOH2C HO HO a-D-Pyranose-form [7282-80-6] Penta-Ac: 1,2,3,4,6-Penta-O-acetyl-a-D-altropyranose [4257-96-9] C16H22O11 390. 343 Mp 118-1198. [a]20 D +63 (CHCl3). Me glycoside: See Methyl altroside, M-149 b-D-Furanose-form [40461-79-8] 1,2-O-Isopropylidene: See 1,2-O -Isopropylidenealtrose, I-59 O HO A-112 a-L-Furanose-form Me glycoside, 2,3-dibenzyl: Methyl 2,3-diO-benzyl-a-L-altrofuranoside [16895-96-8] C21H26O6 374.
M. et al. , Carbohydr. Res. , 1986, 146, C1-C5 (synth, cmr, N-Ac) Likhosherstov, L. M. et al. , Izv. Akad. Nauk SSSR, Ser. Khim. , 1986, 1663-1669; Bull. Acad. Sci. USSR, Div. Chem. Sci. (Engl. Transl. ) , 1986, 1512-1517 (synth, 4-Laspartyl) U. S. Pat. , 1993, five 212 298; CA , 122, 188026 (synth) 4-O -(6-Amino-6-deoxyglucoA-242 pyranosyl)-2,5-dideoxystreptamine [61403-83-6] NH2 CH2 NH2 O OH HO NH2 O OH OH C12H25N3O6 307. 346 Aminoglycoside antibiotic. Isol. from Streptomyces kanamyceticus with 2,5Dideoxystreptamine.