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1 y rearrange to products 4 in the presence of aqueous ammonia.
2 y TFA was reversed by postcolumn addition of aqueous ammonia.
4 l and heteroaryl chlorides and bromides with aqueous ammonia and a hydroxide base to form the primary
5 -acylbenzotriazoles 2a-q efficiently acylate aqueous ammonia and primary and secondary amines to give
8 (TMG) 8 in aceto-nitrile, (ii) concentrated aqueous ammonia at 50 degreesC and (iii) 0.5 mol/dm3sodi
10 bility and energy performance of an advanced aqueous-ammonia-based postcombustion capture process int
11 logues of oligonucleotides with concentrated aqueous ammonia can be completely suppressed by the addi
14 te the advantages, the direct application of aqueous ammonia in the field of transition-metal catalys
15 cobalt(II) solutions were prepared by adding aqueous ammonia into a cobalt(II) nitrate solution in th
23 he resulting sulfinyl chloride solution with aqueous ammonia then provides analytically pure tert-but
26 nce liquid chromatography, were treated with aqueous ammonia, which cleaved the peptide chain on the