与 «ALTROSE»相关的葡萄牙语书籍
在以下的参考文献中发现
altrose的用法。与
altrose相关的书籍以及同一来源的简短摘要提供其在 葡萄牙语文献中的使用情境。
1
ADVANCES IN CARBOHYDRATE CHEMISTRY
Thus, 2,3-di-O-methyl-D-arabinose and 2,3-di-O-methyl-D-altrose give 65% and
80% of the furanose forms respectively, in methyl sulfoxide. The composition of
the equilibrium solution of several sugars as determined by Angyal and
Pickles66 ...
Melville Lawrence Wolfrom, R. Stuart Tipson, 1968
2
Ethylenimine and other aziridines: Chemistry and Applications
ences D-Altrose OMs NHCSZMe Mixed alcs. NaOMe, 1.1 eq. 60 4—5 65 685 D-
Altrose OMs NHBZ EtOH NaOEt 25 90 29 551 D-Altrose OMs NHBZ EtOH NaOEt,
0.27N B.p. 30 72' 551 D-Altrose OMs NHBZ THF'i LiAlH4 B.p. 180 53” 551 ...
3
Química Orgânica – Vol. 2
CHO HO __H H__ OH H__ OH H__ OH CHZOH D-Altrose 25.36 Estes são os
anômeros mais estáveis das formas piranosídicas da D-glicose, D-manose e D-
galactose: OH Ho HocH2 HocH2 cHzoH Ho O Ho /O O Ho oH Ho Ho oH Ho oH
HO ...
4
ADVANCES IN CARBOHYDRATE CHEMISTRY
3-methyl-, phenylosazone, I, 73 —, 2-methyl-3,6-anhydro-, I, 72 —, 2,3,4,6-
tetramethyl-, I, 73 -—, 2,4,6-trimethyl-, I, 73 —, 3,4,6-trimethyl-, I, 73 a-n-Altrose, 4,
6-dimethyl-, and phenylosazone, I, 73 —, 1,2,3,4,6-pentaacetyl-, I, 53, 72 fl-D-
Altrose, ...
Claude S. Hudson, Sidney M. Cantor, 1951
5
Chemistry of The Carbohydrates
The available evidence78 indicates that the anhydro derivative has the unique
structure of 2,3-anhydro-sedoheptuloheptanose with 2,3 and 2,6 rings. The sugar
has been suggested as a source for D-altrose and D-ribose since it is easily ...
Unknown AEHLERT, William Ward Pigman, 1948
6
High Pressure Bioscience and Biotechnology
Sugars Percent viability (S.D.) with different The mean sugar solution
concentrations number of Concentration equatorial OH (mol/l) 0.5 1.0 2.0 groups
§ Control 100 100 100 — D-Altrose - 86 * - 2.6 D-Fructose 86 (4.4) 75 (1.7) 41 (
2.7) 3.0 ...
Claude Balny, R. Hayashi, 1996
7
Introduction to General, Organic and Biochemistry
Additional Problems 20.61 □ 2,6-Dideoxy-D-altrose, also known as D-digitoxose
, is a monosaccharide obtained from the hydrolysis of digitoxin, a natural product
extracted from purple foxglove (Digitalis purpurea). Digitoxin has found wide ...
Frederick Bettelheim, William Brown, Mary Campbell, 2009
(0 Out of the D-allose and D-altrose obtained from D-ribose, the one that gives an
optically inactive acid (allomucic acid) on oxidation is allose while the other
which gives optically active (talomucic) acid is altrose. Hence 7 is allose and 8 is
...
9
Proceedings of the Ninth International Symposium on ...
The effects on the macrocycle of changing one altrose unit in la along the 4C, —
> °S2 — > 'C4 pathway can be monitored within a reasonable nanosecond time
frame by using constrained MD techniques: two pyranose ring torsion angles ...
Juan José Torres Labandeira, José Luis Vila-Jato, 1999
10
Practical Synthetic Organic Chemistry: Reactions, ...
Q|-| HO OHO OH OH OH HO O \ -O H OH H O HO cH2oH OH 0H OH OH D-
altrose oi oi-D-altrofuranose oi-D-altropyranose oi-D-altroseptanose oi-D-altrose
O OH WI oH oH HOW ' OH Ho 9H oH /\/K/?\ OH ... 4 HO e e CH0 B oH OH OH Ho
O ...
