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Reduction of aromatic nitro compound to amines with BER in catalyzing with transition metal compounds

✍ Scribed by Jia Wei Chen; Zhanghuang Xu; Jilong Jiang; Cai Qin Qin

Publisher
Elsevier Science
Year
1991
Weight
50 KB
Volume
15
Category
Article
ISSN
0923-1137

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πŸ“œ SIMILAR VOLUMES

Simple and chemoselective reduction of a
Simple and chemoselective reduction of aromatic nitro compounds to aromatic amines: reduction with hydriodic acid revisited
✍ J.S.Dileep Kumar; ManKit M Ho; Tatsushi Toyokuni πŸ“‚ Article πŸ“… 2001 πŸ› Elsevier Science 🌐 French βš– 82 KB

Reduction of aromatic nitro compounds to amines with hydriodic acid was reinvestigated. Under a milder non-refluxing condition (at 90Β°C for 2-4 h), the reduction proceeded efficiently with excellent chemoselectivity without affecting other functional groups including nitrile, ester, halide, carbonyl

Reduction of organic compounds with sodi
Reduction of organic compounds with sodium borohydride-transition metal salt systems : Reduction of organic nitrile, nitro and amide compounds to primary amines
✍ Toshio Satoh; Shuichi Suzuki; Yoshio Suzuki; Yutaro Miyaji; Zenjiro Imai πŸ“‚ Article πŸ“… 1969 πŸ› Elsevier Science 🌐 French βš– 180 KB

Sodium borohydride is well known as one of the most excellent reducing agents for ketones, acid halogenides and some kinds of esters (1). The reagent, however, has no ability to reduce nitriles, amides and nitro compounds to corresponding