Well-defined cobalt(II)-catalyzed synthesis of perimidine derivatives via acceptorless dehydrogenative annulation.

IF 2.9 3区 化学 Q1 CHEMISTRY, ORGANIC Organic & Biomolecular Chemistry Pub Date : 2024-10-08 DOI:10.1039/d4ob01306a
Debjyoti Pal, Rajashri Sarmah, Avijit Mondal, Itu Mallick, Dipankar Srimani
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Abstract

The versatility of the perimidine moiety offers a rich playground for researchers in fields ranging from medical science to industrial chemistry. Herein, we describe the first Co-catalyzed synthesis of 2,3-dihydro-1H-perimidine via acceptorless dehydrogenative annulation (ADA). Apart from featuring benzyl alcohol having different functionalities, heteroaryl and aliphatic alcohols also provide good yields. Our catalytic protocol is also suitable for different fatty alcohols for furnishing perimidine derivatives, keeping distal unsaturation intact. Several kinetic and control tests were carried out in order to understand the reaction sequence.

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在钴(II)催化下,通过无受体脱氢环化合成明确的包嘧啶衍生物。
从医学科学到工业化学领域,包嘧啶分子的多功能性为研究人员提供了一个丰富的舞台。在此,我们首次介绍了通过无受体脱氢环化(ADA)共同催化合成 2,3-二氢-1H-哌啶的过程。除了具有不同官能度的苄醇外,杂芳基和脂肪醇也能提供良好的产率。我们的催化方案也适用于不同的脂肪醇,在保持远端不饱和度不变的情况下生成包嘧啶衍生物。为了了解反应顺序,我们进行了一些动力学和控制测试。
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来源期刊
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry 化学-有机化学
CiteScore
5.50
自引率
9.40%
发文量
1056
审稿时长
1.3 months
期刊介绍: The international home of synthetic, physical and biomolecular organic chemistry.
期刊最新文献
Back cover P-Stereodefined morpholino dinucleoside 3',5'-phosphorothioates. Synthesis of N-heterocyclic amides from imidazoheterocycles through convergent paired electrolysis. Synthesis of ω-functionalized ketones from strained cyclic alcohols by ring-opening and cross-recombination between alkyl and N-oxyl radicals. Back cover
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