Results 141 to 150 of about 266,703 (209)
ChemInform Abstract: Synthesis of 2‐Arylethylamines by the Curtius Rearrangement. [PDF]
AbstractNovel chemical syntheses of amphetamines (V), (VIII) and (XV) as well as wescaline (XI) using the Curtius rearrangement as key reaction are developed.
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Improved Preparation of Tyramine by Curtius Rearrangement
Chinese Journal of Chemistry, 2009AbstractAn improved and facile preparation of tyramine [2‐(p‐hydroxyphenyl)ethylamine] was described, which starts from phenol and acrylonitrile to form β‐(p‐hydroxyphenyl) propionic acid via Friedel‐Craft's alkylation and nitrile hydrolysis. After hydrazinolysis and a subsequent Curtius rearrangement, tyramine was obtained in 30.2% total yield.
Li-Xin Wang+5 more
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, 2020
A practical and highly efficient protocol for the production of Autotaxin (ATX) inhibitor Ziritaxestat (1) was described.
Hongrui Lei+6 more
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A practical and highly efficient protocol for the production of Autotaxin (ATX) inhibitor Ziritaxestat (1) was described.
Hongrui Lei+6 more
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Curtius-type rearrangement of a sulphonyl azide
Journal of the Chemical Society D: Chemical Communications, 1969Six products have been identified from the thermolysis of mesitylene-2-sulphonyl azide in dodecane: two are derived from a Curtius-type rearrangement of the corresponding sulphonyl nitrene.
Rudolph A. Abramovitch, W. D. Holcomb
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ChemInform, 2011
AbstractThe method avoids the isolation of the potentially hazardous azide intermediate and can be scaled up as an industrial process.
Bojan P. Bondzic+3 more
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AbstractThe method avoids the isolation of the potentially hazardous azide intermediate and can be scaled up as an industrial process.
Bojan P. Bondzic+3 more
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ChemInform Abstract: The Use of Curtius Rearrangement in the Synthesis of 4‐Aminothiazolidines.
ChemInform, 1999AbstractChemInform 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 “Full Text” option. The original article is trackable via the “References” option.
Edson R. Costenaro+2 more
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Curtius-Type Rearrangement of Sulfinyl Azides: A Matrix Isolation and Computational Study.
Journal of Physical Chemistry A, 2022The highly unstable methyl sulfinyl azide, CH3S(O)N3, has been synthesized and characterized for the first time. In the gas phase, CH3S(O)N3 decomposes quickly at room temperature (300 K) with an estimated half-life (t1/2) of 7 min.
Zhuang Wu, Xiaoqing Zeng
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Journal of Organic Chemistry, 2019
Herein we report, a single pot multi-step conversion of inactivated carboxylic acids to various N-containing compounds using a common synthetic methodology, involving diphenyl phosphinic chloride as an activator and sodium azide as a source of nitrogen ...
Arun Kumar+4 more
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Herein we report, a single pot multi-step conversion of inactivated carboxylic acids to various N-containing compounds using a common synthetic methodology, involving diphenyl phosphinic chloride as an activator and sodium azide as a source of nitrogen ...
Arun Kumar+4 more
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The curtius rearrangement of isomeric cycloheptatrienecarboxylic and norcaradienecarboxylic acids
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 19571. The Curtius rearrangement in isomeric β- and γ-cycloheptatrienecarboxylic acids and norcaradlenecarboxylic acid was studied. It was shown that rearrangement goes without isomerization of the migrating hydrocarbon radical under the conditions employed. 2.
I. S. Akhrem+3 more
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An Improved Synthesis of Urea Derivatives from N-Acylbenzotriazole via Curtius Rearrangement
Synthesis, 2019The good leaving tendency of the benzotriazole moiety has been exploited for the synthesis of symmetric, unsymmetric, N-acyl, and cyclic ureas in good yields from N-acylbenzotriazoles by treating the latter with various amines in the presence of TMSN3 ...
A. Singh+4 more
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