An article Beckmann rearrangement: Thiamine hydrochloride as a remarkable catalyst for one-pot synthesis of amides from ketones WOS:000530096600002 published article about ONE-STEP SYNTHESIS; CYCLOHEXANONE-OXIME; SOLVENT-FREE; ORGANIC-SYNTHESIS; NONCATALYTIC BECKMANN; SUPERCRITICAL WATER; EPSILON-CAPROLACTAM; EFFICIENT PROMOTER; REUSABLE CATALYST; IONIC LIQUIDS in [Mahajan, Sheena; Slathia, Nancy; Kapoor, Kamal K.] Univ Jammu, Dept Chem, Jammu 180006, India in 2020.0, Cited 74.0. The Name is 4′-Hydroxyacetophenone. Through research, I have a further understanding and discovery of 99-93-4. Computed Properties of C8H8O2
Thiamine hydrochloride catalyzed synthesis of amides from ketones including 3-acetyl coumarin via Beckmann rearrangement has been reported. The reaction is believed to involve oxime formation, cleavage of C-C bond followed by C-N bond formation in one-pot. Thiamine hydrochloride is stable, cheap, easy to handle and environmentally friendly. (C) 2020 Elsevier Ltd. All rights reserved.
About 4′-Hydroxyacetophenone, If you have any questions, you can contact Mahajan, S; Slathia, N; Kapoor, KK or concate me.. Computed Properties of C8H8O2
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Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles