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Synthesis 1993; 1993(1): 121-125
DOI: 10.1055/s-1993-25813
DOI: 10.1055/s-1993-25813
paper
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved.
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data processing and storage.Reductive N-Monoalkylation of Primary Aromatic Amines
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Publikationsdatum:
17. September 2002 (online)
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Primary aromatic amines 1 with a variety of ring substituents are easily converted to their N-monoalkyl derivatives 3 by a simple variation of the sodium borohydride/sulfuric acid/carbonyl compound procedure previously described for their N-permethylations. The procedure is suitable for the α-monodeuterium labelling of the new N-substituent.