Examples of 'addition product' in a sentence

Meaning of "addition product"

addition product - the result of adding two or more numbers or quantities together

How to use "addition product" in a sentence

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Advanced
addition product
The syn addition product usually predominates.
Deprotecting the addition product.
The present invention relates generally to a process for the preparation of a mercaptan addition product.
An iodinated addition product is thus obtained.
In this case a slight increase in the amount of six addition product was observed.
Deprotecting the addition product occurs under acidic condition.
Too low a degree of quaternization does not permit dispersing the addition product correctly.
This separation agent is an addition product modified with ethylene oxide.
Chlorosulfonic acid may be substituted for sulfur trioxide in preparing the addition product reactant.
Deprotecting the addition product may occur under acidic condition.
The process further comprises hydrolyzing the mercaptan addition product to produce HMBA.
The addition product can be reduced to provide a compound of Formula I.
Attaching the Michael addition product to a polymer matrix.
NMR analysis revealed that the isolated crude was the double sulfonyl chloride addition product.
A small amount of Markovnikov addition product was also observed by NMR.

See also

An addition product of a diolefinic alkylated or alkenylated cyclic hydrocarbon, or.
An iodine-containing addition product is thus obtained.
An addition product consisting of a mixture of mono, di and tri derivatives is obtained.
In a number of studies, a dehydration of the initial addition product has been observed.
Iv The Michael addition product of a dialkylaminoalkyl acrylate with an amino alcohol.
Extraction with an organic solvent, in order to recover said electrophilic addition product.
The coating of the addition product will in general be effective for,.
The term " paroxetine salt " is used to describe an acid addition product of paroxetine.
An addition product of a phenol and a diolefinic alkylated or alkenylated cyclic hydrocarbon ; or.
In some embodiments, deprotecting the addition product occurs under acidic condition.
Thus, the addition product may be retained within the cavity of the host.
The addition of a p-toluenesulfonamide ethylene oxide addition product is effective against the bronze phenomenon.
Accordingly, various reactions can favorably be carried out by using the alkylene oxide addition product.
It will be appreciated that the addition product and the host may separate ( dissociate ).
Furthermore, more desirable are acid catalysts which rarely cleave the raw alkylene oxide addition product.
The simplest such Michael addition product is beta-acryloxypropionic acid.
Reacting with R8SH in the presence of a suitable catalyst, to yield the desired addition product.
Process ( f ) The solid addition product obtained as described above is heated and melted.
Conditions for the O-methylation of the aldol addition product were also identified.
An addition product is thus obtained, of formula,.
Without the DNA, the catalyst gave rise to formation of the aza-Michael addition product.
A small amount of Markovnikov addition product was also observed by NMR . EXAMPLE 8.
Isolated both unreacted starting material, the mono ( desired ) and the bis addition product.
The process of item 20, wherein deprotecting the addition product occurs under acidic condition.
The required five addition products 3 and 4 were isolated along with the six addition product 5.
A formulation of claim 1, wherein the compound is a Michael addition product of the compound of formula I.
An addition product of phenol and a-pinene ;.
In other embodiments, the compound is Michael addition product of Withaferin A.
The 1,4-conjugate addition product is then isolated by art recognized techniques.
Sodium methoxide in methanol / THF for 10 days afforded the second Michael addition product.
The reference discloses that the addition product may be thermolyzed at temperatures up to 150°C.
Addition product of ethylene diamine and propylene oxide OH 770.
The yield of the addition product was about 55 %.
This latter system was, however, remarkably Selective for the 1:1 addition product.
More preferably, the addition product should be about 98 % pure.

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Examples of using Product
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