New calcium antagonists: synthesis, X-ray analysis, and smooth muscle relaxing effect of 3-[ O -(Benzyl-substituted)-oximino-ethers]-hexahydroazepin-2,3-diones. Hydroxylamine- Journal of Synthetic Organic Chemistry, Japan. In this reaction the carboxylic acid adds to the DCC molecule to form a good leaving group which can then be displaced by an amine during nucleophilic substitution. Citations are the number of other articles citing this article, calculated by Crossref and updated daily. You’ve supercharged your research process with ACS and Mendeley! ITS USE IN ORGANIC SYNTHESIS. The direct conversion of a carboxylic acid to an amide is difficult because amines are basic and tend to convert carboxylic acids to their highly unreactive carboxylates. A base-mediated self-propagative Lossen rearrangement of hydroxamic acids for the efficient and facile synthesis of aromatic and aliphatic primary amines. You’ve supercharged your research process with ACS and Mendeley! Oliver Kreye, Hatice Mutlu, Michael A. R. Meier. Recognition of Hg2+ Ion through Restricted Imine Isomerization: Crystallographic Evidence and Imaging in Live Cells ITS USE IN ORGANIC SYNTHESIS. A. V. Velikorodov, E. N. Kutlalieva, N. N. Stepkina, E. A. Shustova, O. Yu. Lossen Rearrangements under Heck Reaction Conditions. Yujiro Hoshino, Naoya Ohtsuka, Kiyoshi Honda. These metrics are regularly updated to reflect usage leading up to the last few days. Rearrangement de tiemann des amidoximes synthese de carbodiimides. In lieu of an abstract, this is the article's first page. New calcium antagonists: synthesis, X-ray analysis, and smooth muscle relaxing effect of 3-[ O -(Benzyl-substituted)-oximino-ethers]-hexahydroazepin-2,3-diones. A convenient method for the preparation of hydroxamic acids.
One-pot synthesis of primary amines from carboxylic acids through rearrangement of in situ generated hydroxamic acid derivatives. https://doi.org/10.1134/S1070428020090110, https://doi.org/10.5059/yukigoseikyokaishi.75.746, https://doi.org/10.1016/j.tetlet.2016.10.037, https://doi.org/10.1002/047084289X.rh058.pub2, https://doi.org/10.1002/9780471264194.fos05731, https://doi.org/10.1002/9780470125946.ch7, https://doi.org/10.1007/978-3-322-96805-0_12, https://doi.org/10.1016/S0040-4039(00)01058-3, https://doi.org/10.1016/S0968-0896(99)00090-5, https://doi.org/10.1080/00304949609356535, https://doi.org/10.1007/978-3-322-94726-0_66, https://doi.org/10.1016/S0040-4039(00)61187-5, https://doi.org/10.1016/B978-0-08-092553-0.50044-3, https://doi.org/10.1016/B978-0-08-052349-1.00172-4, https://doi.org/10.1016/B978-0-08-092558-5.50018-6, https://doi.org/10.1080/00397918308082718, https://doi.org/10.1016/B978-0-08-092556-1.50017-8, https://doi.org/10.1080/00304948209354920, https://doi.org/10.1016/0301-0104(76)87039-5, https://doi.org/10.1016/B978-0-12-618553-9.50018-3, https://doi.org/10.1016/S0040-4039(00)99740-5.
Yujiro Hoshino, Naoya Ohtsuka, Takuya Okada, Kiyoshi Honda.
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