Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Adonose

Bacterial oxidation of ribitol (adonitol XXX) affords L-adonose or L-erythropentulose (XXXI) (c/. the bacterial oxidation of sorbitol to L-sorbose). By the agency of methyl alcoholic hydrogen chloride, XXXI yields methyl L-adonoside (XXXII) and condensation of the... [Pg.103]

The oxidation of a secondary alcoholic group in the presence of primary alcoholic groups by Acetobacter suboxydans converts adonit into adonose [1041]. The treatment of androstenediol and dehydroandrosterone with yeast yields A -androstenedione [1088]. Steroidal hydroxy ketones are dehydrogenated to dicarbonyl compound with CorynebacteriUlh simplex [1056] (see equations 446 and 447). Examples of oxidations of secondary alcohols to ketones are shown in equations 265-268. [Pg.146]

Another example of the preferential oxidation of secondary hydroxyls versus primary hydroxyls is the formation of L-adonose from L-adonit by bakers yeast (Acetobacter suboxydans) (equation 291) [1041]. [Pg.157]

D-Ribulose. D. erythro.2-Pentulosc D-adonose D-erythro-2-ketopentose. C5Hl0O5 mol wt 150.13. C... [Pg.1306]

Ribulose. Riboketose. Adonose. Erythro-pentulose. Arabulose. Arabinulose. Arabo-... [Pg.815]

Adonitol, R-94 Adonose, P-47 eADP, R-110 ADP, A-33 ADPG, A-36 ADPR, A-37 Adriacin, A-58 Adriamycin, A-58 Adriamycinol, A-58 Adriamycinone, A-58 Adriblastin, A-58 AE-cellulose, C-48 Aediirid, E-2 Aerosporin, S-86 AF, A-879... [Pg.995]

Adamantanes, A33, A37, Z9 Adenocarpin, K18 Adianine, T43 Adiantol, T45 Adipedatol, T45 Adonose, C2 Adrenaline, A22 Adrenochrome, A24 Adriamycin, Y28 Aeroplysinins, Y19, YIO Aflatoxins, Y13 Agarofurans, T19 Agatharesinol, Y9 Ageratriol, T5 ... [Pg.157]


See other pages where Adonose is mentioned: [Pg.103]    [Pg.323]    [Pg.86]    [Pg.2591]    [Pg.2747]    [Pg.236]    [Pg.460]    [Pg.460]    [Pg.27]    [Pg.301]    [Pg.2845]    [Pg.2546]   
See also in sourсe #XX -- [ Pg.2 ]




SEARCH



L-Adonose

© 2024 chempedia.info