Examples of 'yield compound' in a sentence

Meaning of "yield compound"

yield compound: This phrase is unclear without additional context. It could potentially relate to a chemical reaction, financial investment, or agricultural term where "yield" and "compound" have specific meanings.

How to use "yield compound" in a sentence

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yield compound
The solvent was evaporated from the collected fractions under a reduced pressure to yield Compound No.
The filtrate was concentrated to yield compound 6 as a yellow solid.
The resultant residue is purified by column chromatography to yield compound 6.
The solvent was evaporated to yield compound 13 as a white solid.
The product is then cleaved of the solid phase support to yield compound 7.
The mixture was concentrated in vacuo to yield Compound 1 ( 4 g ) as a white solid HCl salt.
The obtained yellow solid was dissolved in water and lyophilized to yield compound 11.
The combined filtrates were concentrated to yield compound la as a light yellow residue ( 392 g ).
The alcohol moieties are then protected with benzyl groups to yield compound 1.
The solution was evaporated to yield Compound 3 650 mg as a yellow solid.
This compound was silylated and oxidized to yield compound 4.
To yield Compound 8.
The crude mixture was acetylated to yield compound 8a.
The latter is readily cyclized to yield compound having formula 1.
The residue was co-evaporated four times with toluene and dried in vacuo to yield compound 5.

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The solid was allowed to air dry to yield compound 25 as a white solid.
The reaction is quenched with water and extracted with dichloromethane to yield compound 2.
The residue was purified by RP-HPLC to yield Compound 13i as a white powder.
The resulting indole derivative may further be subjected to process E to yield compound ( I ).
The solid is further dried over vacuum to yield compound clxxxxv ( 95 % ) as white powder.
The amide is subsequently subjected to hydrogenation conditions to yield Compound 2.
The solution was then evaporated to yield Compound 4 as a yellow solid ( 2 g ).
The mixture was evaporated to dryness and further dried by lyophilization to yield Compound 64.
The precipitate was collected by filtration to yield Compound 2 as a white solid HCl salt ( 200 mg ).
In step 3, compound 4 is reacted with dibromoethane under basic conditions to yield compound 5.
The filtrate was concentrated in vacuo to yield Compound 12f as an oil.
The resultant slurry is filtered, washed with aqueous solvent, and dried to yield compound 5.
The residue was purified vía RP-HPLC to yield Compound 12d as an oil.
After the solvent was evaporated, the residue was purified vía RP-HPLC to yield Compound 36a.
Compound 30 is alkylated with the alkyl halide 31 to yield compound 32 under standard conditions.
Compound 22 is then cyclized vía a Diels-Alder reaction, followed by treatment with a base to yield Compound 21.
Conducting a functional group interconversion reaction to yield Compound II above ; wherein,.
The solvent is evaporated under reduced pressure to yield compound 9.
The filtrate was evaporated to yield Compound 17d.
Compound 8 is subsequently reacted with a phosphate ester, such as a dialkyl halophosphate, to yield Compound 7A.
Ester 18 is subsequently cyclized to yield Compound 17 as follows.
Converting the amine group on compound 3 to a methoxy group to yield compound and.
The solution was concentrated and purified using column chromatography conditions to yield compound 31 as a solid.
The resulting solution was lyophilized to yield Compound 2b.
It was dried over magnesium sulfate, filtered and concentrated to yield compound M2D.
A cyanide group displaces the chloride to yield compound 20.
Compound 5 is then deprotected to yield compound 6.
The second step is the debenzylation of compound 7 to yield compound 8.
Collect the solid by filtration and dry in vacuo to yield compound ( 4 ).
The amino group was further protected using Boc2O to yield compound 53.
The crude product is purified using radial chromatography to yield compound 244.
The intermediate trifluroacetate ( not shown ) is hydrolyzed during isolation to yield compound 24 directly.
The resultant crude residue is purified using flash chromatography to yield compound 295.
Compound 2 is subsequently cyclized to yield Compound 1.
The filtrate was concentrated in vacuo to yield Compound 23c.

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