Examples of 'grignard' in a sentence
Meaning of "grignard"
Grignard is a noun that likely refers to a chemical compound or reaction, commonly used in organic chemistry processes or experiments
Show more definitions
- A French surname.
How to use "grignard" in a sentence
Basic
Advanced
grignard
Grignard reagents add to the carbonyl center.
Preferred methylating agents include methyl grignard and methyllithium.
Grignard reagents are very useful in organic synthesis.
To this solution was added the above freshly prepared grignard reagent.
Grignard salt of lactam may be useful as a catalyst.
The mixture was heated to reflux to prepare the grignard reagent by a literature method.
Grignard reagents and alkyllithium reagents are preferred.
Three equivalents of the vinyl grignard reagent are also necessary for good yields.
Grignard was the son of a sail maker.
The solution of Grignard reagent was then obtained.
Grignard reagents are notorious for having induction periods.
The preparation of Grignard reagents is well known.
Grignard reagents may be similarly titrated.
The most preferred Grignard reagent is methylmagnesiumchloride.
Grignard addition generates ketone iii.
See also
Methylmagnesium chloride is a commercially available Grignard reagent.
Grignard reagents are very reactive.
The conversion is similar to the Grignard reaction.
Grignard reagents add to propylene oxide to give secondary alcohols.
Preferably the organometallic reagent is a Grignard reagent.
Grignard type reactions are very important reactions in preparative chemistry.
The basic reagent may be a Grignard reagent.
Grignard reaction in addition to other reactions involving organometallic reagents.
This reagent was assayed for Grignard content.
Grignard agents react.
Such reagents are also known as Grignard reagents.
Grignard reactions in microreactors.
Examples of nucleophiles are Grignard reagents and organolithium reagents.
Grignard reagents and their formation are well known in the art.
Formation of the Grignard reagent is complete.
Grignard reagents react with carbonyl groups to secondary and tertiary alcohols.
In such solvents the Grignard reagent is relatively soluble.
Grignard reactions on the aldehyde provides a route to a variety of substituted hydroxymethyl analogs.
By reacting a Grignard reagent with dioxane.
Grignard reagents would yield magnesium derivatives which would be another alternative.
A solution of carbonyl compound is added to the Grignard reagent.
Grignard reagents and organolithium compounds react with MeCHO to give hydroxyethyl derivatives.
They are commonly found as Grignard reagents.
The reaction is a double grignard synthesis and introduces the spiro ring onto the bicyclic nucleus.
Magnesium similarly metalates organohalides to give Grignard reagents.
It forms a Grignard reagent and organolithiuim compound.
A temperature rise was observed when Grignard reaction initiated.
Grignard is located directly adjacent to the Southwest.
The mixture was heated to start the Grignard formation.
The Grignard reaction is preferably conducted in tetrahydrofuran.
This can be accomplished by using different Grignard reagents.
The Grignard reagent of thiazole is commercially available.
Alternatively the magnesium Grignard reagent can be used.
A Grignard reagent is an organometallic compound containing magnesium.
Under suitable conditions Grignard compounds can be stored as such.
