Examples of 'sodium methoxide in methanol' in a sentence
Meaning of "sodium methoxide in methanol"
sodium methoxide in methanol - This phrase refers to a chemical compound composed of sodium methoxide dissolved in methanol. It is a substance used in various chemical processes and reactions
How to use "sodium methoxide in methanol" in a sentence
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sodium methoxide in methanol
Deacetylation was effected using sodium methoxide in methanol.
Sodium methoxide in methanol.
Preferred reaction conditions are the use of sodium methoxide in methanol at reflux.
Sodium methoxide in methanol is an example of one such alkoxide and solvent.
The resulting orthoester is then debenzoylated with sodium methoxide in methanol.
Sodium methoxide in methanol was charged and the mixture was stirred until reaction completion.
The trimethylsilyl group can be removed using a base such as sodium methoxide in methanol.
Preferably, sodium methoxide in methanol is used.
The catholyte solution in the catholyte compartment 20 included sodium methoxide in methanol.
Preferably, solutions of sodium methoxide in methanol at reflux.
Sodium methoxide in methanol is added to the reaction vessel, which is then heated.
Preferably, solutions of sodium methoxide in methanol under reflux are used.
The base may be added as a solution, for example sodium methoxide in methanol.
Preference is given to using sodium methoxide in methanol or potassium tert-butoxide in tert-butanol.
R1a fluoro may be converted to methoxy by treatment with sodium methoxide in methanol.
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Deprotection using methanolic ammonia or sodium methoxide in methanol yields the corresponding compound of formula 27.
The buffer solution in the buffer compartment 24 included sodium iodide and sodium methoxide in methanol.
Deprotection using methanolic ammonia or sodium methoxide in methanol yields the desired products of formula 1.
Deprotection of the C29 acetoxy group is then accomplished using sodium methoxide in methanol.
Treatment with sodium methoxide in methanol was carried out as in Example 1.
Most preferred is a solution of about 25 % sodium methoxide in methanol.
A 25 wt % solution of sodium methoxide in methanol was added dropwise to pH 11.
Preference is also given to 30 % strength sodium methoxide in methanol.
Treatment of JJ-1 with sodium methoxide in methanol yields the final product JJ-2.
Most preferably, the ring closure is carried out using a 30 % solution of sodium methoxide in methanol.
Prior art syntheses of d4T generally use sodium methoxide in methanol to achieve the 5 ' - deprotection.
Heat the reaction mixture at 85°C with the slow addition of sodium methoxide in methanol.
To this solution 42 g of sodium methoxide in methanol is added over a period of 15 min.
Treat the dry solution at about 85°C with the slow addition of sodium methoxide in methanol.
Treatment of PP-1 with sodium methoxide in methanol yields the final product PP-2.
This mixture was added to a freshly prepared solution of 60 ml ( 2M ) of sodium methoxide in methanol.
Another equivalent of 25 % sodium methoxide in methanol was added.
The product of this step was refluxed with sodium methoxide in methanol for 20 h.
An additional 26 mL of 25 percent sodium methoxide in methanol was then added.
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