Examples of 'alcohol of formula' in a sentence
Meaning of "alcohol of formula"
alcohol of formula: This phrase does not have a commonly recognized meaning in English and may be a result of mistranslation or a typo. It is not clear in what context this phrase would be used
How to use "alcohol of formula" in a sentence
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alcohol of formula
Reduction of a compound of formula IVa provides an alcohol of formula IVb.
Oxidation of an alcohol of Formula Ic provides a carboxaldehyde of Formula Id.
Concentration in vacuo gave the alcohol of formula II.
A protected alcohol of Formula XXIV is prepared by the procedure shown in Reaction Schemes 1 or 2.
Alternatively said aldehyd may be prepared by oxidation of alcohol of formula XXVI.
After aqueous workup, the allylic alcohol of formula 9 can be used without further purification.
Reduction of a compound of formula Ib provides an alcohol of formula Ic.
In this approach, an alcohol of formula XXX is treated with iodine.
Step B involves the reduction of an ether of formula 2 to obtain an alcohol of formula 3.
Step E involves the iodination of an alcohol of formula 5 to obtain an iodide of formula 6.
Step D involves the oxidative hydrolysis of an ether of formula 4 to an alcohol of formula 5.
Step B involves the etherification of an alcohol of formula 2 to obtain an ether of formula 3.
Step B involves the reduction of an aldehyde of formula 2 to obtain an alcohol of formula 3.
Step C involves the alkylation of an alcohol of formula 3 to obtain an ether of formula 4.
Step F involves the hydrolysis of a diene of formula 6 to obtain an alcohol of formula 7.
See also
Step D involves the oxidation of an alcohol of formula 4 to obtain an aldehyde of formula 5.
Step B involves the reduction of an imide of formula 1 to obtain an alcohol of formula 3.
Step G involves the mesylation of an alcohol of formula 3 to obtain a mesylate of formula 7.
Step E involves the reduction of a carbamate of formula 5 to obtain an alcohol of formula 6.
Step B involves the alkylation of an alcohol of formula 2 to obtain an alcohol of formula 3.
An intermediate particularly adapted for such a stereospecific synthesis is the alcohol of formula ( V ) above.
The alcohol of formula ( III ) may itself be prepared by the processes described in Scheme I.
Oxidizing a corresponding alcohol of formula III ;.
The allylic alcohol of formula 16 can then be diastereoselectively epoxidized.
Protection of the OH group of the alcohol of formula 3 with a group Y.
At least one alcohol of formula ( I ) that will be defined in detail later and.
For example, the reaction is carried out using an alkoxide of an alcohol of formula ( a ).
For example, the allyl alcohol of formula 5 can be treated with a phosphorus trihalide e . g.
A process for preparing a bisfuran alcohol of Formula 0,.
The chiral amino alcohol of formula ( IV ) is a derivative of norephedrine.
Treating with an oxidizing agent an alcohol of formula STR40.
At least one alcohol of formula ( I ) below or optical isomers thereof,.
Subsequent hydrogenation provides an alcohol of formula ( XX ).
The ethylenically unsaturated alcohol of formula II is selected from hydroxyalkyl ( meth ) acrylates ;.
And then the optically active amino alcohol of formula ( IV ).
The alcohol of Formula ( 36 ) is concentrated and purified by techniques well known in the art.
With a reducing agent to form an alcohol of formula ( III ).
Reacting the alcohol of formula II, with a silyl compound of formula III,.
Mention may be made of EIOH, as an example of a heterocyclic alcohol of formula ( III ).
Step I involves the silylation of an alcohol of formula 10 to obtain a silyl ether of formula 11.
In one embodiment, the carbonyl-forming method comprises the use of a secondary alcohol of formula ( Ia ).
Protecting the OH group of the alcohol of formula 3 with a group Y ;.
The primary alcohol of Formula 10 is the starting material indicated in Reaction Scheme 1.
From the viewpoint of thermal resistance, a hindered alcohol of formula ( I ) is particularly excellent.
Combining the bisfuran alcohol of Formula 0 with disuccinimidyl dicarbonate to form a compound of Formula L1,.
Reduction of the acid of Formula 30 then provides the alcohol of Formula 31a as the phenol.
An alcohol of formula in which the symbols R1 to R4 are as defined in claim 1.
The higher ketone is then hydrogenated to an alcohol of formula ( C1 ).
Independently, a benzyl alcohol of formula ( 5b ) may be prepared as follows.
For a compound of formula I, oxidizing a corresponding alcohol of formula III,.
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