The reaction of 2-irimcihylsilyi-1,2,3-triazole with acid chlorides readily forms iriazuie amides. The wiazole amides, when heated 10 15oOC in suifolane. rearrange wirh rhe elimination of niwngen to give 2-subslituied nxazoles in high yields. The nxazoie synlhesis is general. and can be carried 01~1
One-pot chemoselective reductive alkylation of nitroarenes: A new general method of synthesis of alkylanilines
β Scribed by Giuseppe Bartoli; Marcella Bosco; Renato Dal Pozzo; Marino Petrini
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- French
- Weight
- 391 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0040-4020
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## Abstract For Abstract see ChemInform Abstract in Full Text.
A new, high-yielding methodology for reducing hydrazones to hydrazines is described, which allows the synthesis of different mono-, di-and trisubstituted hydrazines. Moreover, the reduction step can be followed by an in situ reaction with a carboxylic acid making possible a 'one-pot' synthesis of tr
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v