Chemistry of nitrosoimines. XV. Reactions of 3-substituted 2-nitrosoimino-2,3-dihydrobenzothiazoles with lithium aluminum hydride and diazo compounds.
スポンサーリンク
概要
- 論文の詳細を見る
3-Substituted 2-nitrosoimino-2,3-dihydrobenzothiazoles (<B>1</B>) were reduced with lithium aluminum hydride to give the corresponding thiazolone azines and bis[<I>o</I>-(<I>N</I>-substituted <I>N</I>-formylamino)phenyl] disulfides as major products. Reactions of <B>1</B> with some substituted diazomethanes gave the corresponding unsymmetrical azine <I>N</I>-monoxides (<B>16</B>) or azines (<B>17</B>) depending on the structure of the diazomethane.
- 公益社団法人 日本化学会の論文
著者
-
Ochiumi Masahide
Department of Chemistry, Faculty of Science, The University of Tokyo
-
Kawamura Takayuki
Department of Chemistry, Faculty of Science, The University of Tokyo
関連論文
- VORTEX BEHAVIOR OF PULSATING JETS FROM A RECTANGULAR NOZZLE(Flow Control 2)
- Regulation of Skeletal Muscle Peroxisome Proliferator-Activated Receptor γ Expression by Exercise and Angiotensin-Converting Enzyme Inhibition in Fructose-Fed Hypertensive Rats
- Impact of Exercise and Angiotensin Converting Enzyme Inhibition on Tumor Necrosis Factor-α and Leptin in Fructose-Fed Hypertensive Rats
- Effects of Exercise Training on Glomerular Structure in Fructose-Fed Spontaneously Hypertensive Rats
- Changes in the Responsiveness of Melanophores to Electrical Nervous Stimulation after Prolonged Background Adaptation in the Medaka, Oryzias latipes
- A mechanistic study on the reaction of iminothiadiazolines with activated acetylenes: Competitive pathway through hypervalent sulfurane and zwitterion.
- Chemistry of Nitrosoimines. X. Reactions of 3-Substituted 2-Nitrosoimino-2,3,-dihydrobenzothiazoles with Aryl and t-Butyl Grignard Reagents
- Chemistry of Nitrosoimines. XII. Reactions of 3-Substituted 2-Nitrosoimino-2,3-dihydrobenzothiazoles with Alkyl Grignard Reagents
- Chemistry of nitrosoimines. XV. Reactions of 3-substituted 2-nitrosoimino-2,3-dihydrobenzothiazoles with lithium aluminum hydride and diazo compounds.