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The last step of the syntheses involved a strong acidic condition, leading to an unstable product upon storage.
At least some of these amino acid syntheses involved hydrogen cyanide and aldehydes (e.g., formaldehyde) as gaseous intermediates formed from the initial gases.
A primary contributor to the high cost is that the complex, multistep syntheses involved in producing commercial TMT and iTRAQ reagents lead to moderate to low yields.
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Moreover, almost all of the syntheses involving a given solvent fall into the same cluster.
Polymer syntheses involve metal-mediated polymerizations of alkene, alkyne, silane, and/or stannane monomers.
Key steps of the syntheses involve selective N-alkylation of quinolinone derivatives and guanylation of aryl amines.
This new synthesis involved hydroxyethylmethacrylate, a hydroxytelechelic polybutadiene, and 4,4′-methylene-bis cyclohexylisocyanate).
This synthesis involved 1,6-hexanediylbis[oxy 2-hydroxy-3,1-propanediyl)]bisacrylate, a hydroxytelechelic polybutadiene, and 4,4′-methylene-bis (cyclohexylisocyanate).
The key steps in the synthesis involved enzymatic transesterification of 1,3-propanediol derivatives and two consecutive cis-selective Wittig olefinations.
This catalyst-free, low-temperature synthesis involved introducing CO2 and CH4 as reactants at a specified ratio of 2 3.
The synthesis involved the covalent modification of PEI with 4-butylamino-N-carboxymethyl-1,8-naphthalimide BACMN) for getting amphiphilic polymer.
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