Examples of 'free hydroxy' in a sentence
Meaning of "free hydroxy"
free hydroxy: In chemistry, this term refers to hydroxyl groups that are not involved in chemical bonds and are therefore available for reactions. These unbound hydroxyl groups play a crucial role in various chemical processes and reactions
How to use "free hydroxy" in a sentence
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free hydroxy
Stands primarily for a free hydroxy group.
The free hydroxy groups at the phosphorous atoms are acidic.
Optional hemisuccinylation or sulphation of the free hydroxy groups.
Free hydroxy groups or hydroxy groups esterified with a organic or inorganic acid ;.
The infrared spectrum no longer shows free hydroxy groups.
The free hydroxy group can be protected ( reaction step i ) by a suitable ester or ether function.
The ester may have one or more free hydroxy groups.
The remaining free hydroxy groups in compound ( 14 ) are converted with sodium hydride to the alkoxides.
The hydroxy protecting group is then removed to provide the free hydroxy group.
Esterases would liberate the active, free hydroxy compounds once inside the cell.
The two regioisomers were obtained along with mixtures of the free hydroxy analogs.
It is generally desirable to convert the free hydroxy groups to protected hydroxy groups ( X ).
The hydroxy protecting group is readily removed to provide the free hydroxy group.
The free hydroxy optionally contained in R3 may also be transformed into -- SH.
The hydroxy protecting group is subsequently removed to provide the free hydroxy group.
See also
A blend of polymers containing free hydroxy groups comprised of ( A ) and ( B ) as defined in claim 6 ;.
Known depot derivatives of neuroleptics are carboxylic acid esters of neuroleptics comprising a free hydroxy group.
A blend of polymers containing free hydroxy groups comprised of,.
Also described are crystalline forms of Raltegravir free hydroxy.
A cyclodextrin is composed of several glucose units which have three free hydroxy groups per glucose.
The present invention also describes crystalline forms of Raltegravir free hydroxy.
Figure 2 shows in vivo iron mobilisation using the metabolite free hydroxy compounds of the invention.
Step H is a step for forming a mevalonolactone by the dehydration reaction of the free hydroxy acid I-2.
The product was then dried under vacuum at 40°C overnight to obtain Raltegravir free hydroxy Form A3.
Herein a substitution degree of 1 equals a 100 % of substitution of one of the three free hydroxy groups.
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