The esterification of tertiary alcohols using benzotriazole esters typically requires milder conditions compared to other acylation methods. Reactions often proceed at room temperature or slightly elevated temperatures, avoiding the need for harsh reagents and conditions that can lead to side reactions.
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L-Aspartic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 1-(1,1-dimethylethyl) 4-(phenylmethyl) ester
amino-(1-methyl-1h-indol-3-yl)-acetic acid
(2-carboxyethyl) triphenylphosphoniumbromide
1-bromo-4-phenethoxybenzene
1,1'-THIOCARBONYLDI-2(1H)-PYRIDONE
thiophene-2-(N-diphenylphosphino)methylamine
1-Propen-1-amine, N,N-diethyl-3-phenyl-
2-(di(1H-indol-3-yl)methyl)-5-(diethylamino)phenol
{3-[4-(3a,4,5,9b-tetrahydro-3H-cyclopenta[c]quinolin-4-yl)benzoyloxy]propyl}trimethylammonium chloride
Ac-LYRAL-SCH2CH2COOCH3
1-(3-(benzylamino)propyl)pyrrolidin-2-one
1-(furan-2-yl)-2-(thiophen-2-yl)ethane-1,2-dione
