INDIUM MEDIATED REDUCTIVE ACYLATIONS OF NITROARENES TOWARDS N,O -DIACYLATED N -ARYLHYDROXYLAMINES *
β Scribed by Kim, Byeong Hyo; Cheong, Jae Wook; Han, Rongbi; Jun, Young Moo; Baik, Woonphil; Lee, Byung Min
- Book ID
- 120290240
- Publisher
- Taylor and Francis Group
- Year
- 2001
- Tongue
- English
- Weight
- 160 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0039-7911
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π SIMILAR VOLUMES
Anilides are synthesized from nitroarenes via sequential reductive N-acylation, catalyzed by ruthenium compounds in the presence of a carboxylic acid and methyl formate or formic acid. In the reduction step, hydrogen is supplied by the formic compound.
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Nitro-and nitrosoarenescanbe reducedusingbaker'syeast(Saccharomyces cerevkiae) under two distinctsets of conditions,one of whichis in fact a well establishednon-enzymicprocess. In orderto clarify reportsin the literaturea comparisonof the two methedshas beenmade.@ 1997Elsevier ScienceLtd. Recently