Alexander S. Bobkov, Nikita V. Teplyashin, Svetlana V. Martynovskaya, Andrey V. Ivanov, Nadezhda M. Vitkovskaya
{"title":"n -烯基- 1h -吡咯-2-酰基-乙醛与羟胺的反应:机理和取代基影响的量子化学见解","authors":"Alexander S. Bobkov, Nikita V. Teplyashin, Svetlana V. Martynovskaya, Andrey V. Ivanov, Nadezhda M. Vitkovskaya","doi":"10.1002/poc.70023","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>We report on a quantum chemical study (B2PLYP-D3BJ/6-311+G**//B3LYP/6-31+G*) of the mechanism of the reaction of <i>N</i>-allenyl-1<i>H</i>-pyrrole-2-yl-carbaldehydes with hydroxylamine in ethanol leading to pyrrolopyrazine oxides. The main focus is placed on unraveling the influence of the nature of the substituent in the fourth and fifth positions of the pyrrole ring on the kinetic characteristics of the key stages of the reaction, which are oximation and intramolecular cyclization. The aryl substituents are found to favor the reaction, in contrast to the alkyl substituents.</p>\n </div>","PeriodicalId":16829,"journal":{"name":"Journal of Physical Organic Chemistry","volume":"38 7","pages":""},"PeriodicalIF":1.9000,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Reaction of N-Allenyl-1H-Pyrrole-2-Yl-Carbaldehydes With Hydroxylamine: A Quantum Chemical Insight Into the Mechanism and Substituent Influence\",\"authors\":\"Alexander S. Bobkov, Nikita V. Teplyashin, Svetlana V. Martynovskaya, Andrey V. Ivanov, Nadezhda M. Vitkovskaya\",\"doi\":\"10.1002/poc.70023\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n <p>We report on a quantum chemical study (B2PLYP-D3BJ/6-311+G**//B3LYP/6-31+G*) of the mechanism of the reaction of <i>N</i>-allenyl-1<i>H</i>-pyrrole-2-yl-carbaldehydes with hydroxylamine in ethanol leading to pyrrolopyrazine oxides. The main focus is placed on unraveling the influence of the nature of the substituent in the fourth and fifth positions of the pyrrole ring on the kinetic characteristics of the key stages of the reaction, which are oximation and intramolecular cyclization. The aryl substituents are found to favor the reaction, in contrast to the alkyl substituents.</p>\\n </div>\",\"PeriodicalId\":16829,\"journal\":{\"name\":\"Journal of Physical Organic Chemistry\",\"volume\":\"38 7\",\"pages\":\"\"},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2025-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Physical Organic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/poc.70023\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Physical Organic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/poc.70023","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Reaction of N-Allenyl-1H-Pyrrole-2-Yl-Carbaldehydes With Hydroxylamine: A Quantum Chemical Insight Into the Mechanism and Substituent Influence
We report on a quantum chemical study (B2PLYP-D3BJ/6-311+G**//B3LYP/6-31+G*) of the mechanism of the reaction of N-allenyl-1H-pyrrole-2-yl-carbaldehydes with hydroxylamine in ethanol leading to pyrrolopyrazine oxides. The main focus is placed on unraveling the influence of the nature of the substituent in the fourth and fifth positions of the pyrrole ring on the kinetic characteristics of the key stages of the reaction, which are oximation and intramolecular cyclization. The aryl substituents are found to favor the reaction, in contrast to the alkyl substituents.
期刊介绍:
The Journal of Physical Organic Chemistry is the foremost international journal devoted to the relationship between molecular structure and chemical reactivity in organic systems. It publishes Research Articles, Reviews and Mini Reviews based on research striving to understand the principles governing chemical structures in relation to activity and transformation with physical and mathematical rigor, using results derived from experimental and computational methods. Physical Organic Chemistry is a central and fundamental field with multiple applications in fields such as molecular recognition, supramolecular chemistry, catalysis, photochemistry, biological and material sciences, nanotechnology and surface science.