دورية أكاديمية

Ru (II) -catalyzed P (III) -assisted C8-alkylation of naphthphosphines.

التفاصيل البيبلوغرافية
العنوان: Ru (II) -catalyzed P (III) -assisted C8-alkylation of naphthphosphines.
المؤلفون: Ma WT; Collaborative Innovation Center for Advanced Organic Chemical Materials Co-constructed by the Province and Ministry, Ministry of Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules, and College of Chemistry and Chemical Engineering, Hubei University, Wuhan, 430062, China. liuyuejin@hubu.edu.cn., Huang MG; Collaborative Innovation Center for Advanced Organic Chemical Materials Co-constructed by the Province and Ministry, Ministry of Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules, and College of Chemistry and Chemical Engineering, Hubei University, Wuhan, 430062, China. liuyuejin@hubu.edu.cn., Fu Y; Collaborative Innovation Center for Advanced Organic Chemical Materials Co-constructed by the Province and Ministry, Ministry of Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules, and College of Chemistry and Chemical Engineering, Hubei University, Wuhan, 430062, China. liuyuejin@hubu.edu.cn., Wang ZH; Collaborative Innovation Center for Advanced Organic Chemical Materials Co-constructed by the Province and Ministry, Ministry of Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules, and College of Chemistry and Chemical Engineering, Hubei University, Wuhan, 430062, China. liuyuejin@hubu.edu.cn., Tao JY; Collaborative Innovation Center for Advanced Organic Chemical Materials Co-constructed by the Province and Ministry, Ministry of Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules, and College of Chemistry and Chemical Engineering, Hubei University, Wuhan, 430062, China. liuyuejin@hubu.edu.cn., Li JW; Collaborative Innovation Center for Advanced Organic Chemical Materials Co-constructed by the Province and Ministry, Ministry of Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules, and College of Chemistry and Chemical Engineering, Hubei University, Wuhan, 430062, China. liuyuejin@hubu.edu.cn., Liu YJ; Collaborative Innovation Center for Advanced Organic Chemical Materials Co-constructed by the Province and Ministry, Ministry of Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules, and College of Chemistry and Chemical Engineering, Hubei University, Wuhan, 430062, China. liuyuejin@hubu.edu.cn., Zeng MH; Collaborative Innovation Center for Advanced Organic Chemical Materials Co-constructed by the Province and Ministry, Ministry of Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules, and College of Chemistry and Chemical Engineering, Hubei University, Wuhan, 430062, China. liuyuejin@hubu.edu.cn.; State Key Laboratory for the Chemistry and Molecular Engineering of Medicinal Resources, School of Chemistry and Pharmaceutical Sciences, Guangxi Normal University, Guilin, 541004, China. zmh@mailbox.gxnu.edu.cn.
المصدر: Chemical communications (Cambridge, England) [Chem Commun (Camb)] 2022 Jun 23; Vol. 58 (51), pp. 7152-7155. Date of Electronic Publication: 2022 Jun 23.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Royal Society of Chemistry Country of Publication: England NLM ID: 9610838 Publication Model: Electronic Cited Medium: Internet ISSN: 1364-548X (Electronic) Linking ISSN: 13597345 NLM ISO Abbreviation: Chem Commun (Camb) Subsets: PubMed not MEDLINE; MEDLINE
أسماء مطبوعة: Original Publication: Cambridge : Royal Society of Chemistry
مستخلص: We report a phosphine-directed ruthenium-catalyzed C8-selective alkylation of naphthalenes with alkenes. This protocol provides straightforward access to a large library of electron-rich C8-alkyl substituent 1-naphthphosphines, which outperformed common commercial phosphines and their precursors in the Pd-catalyzed Suzuki-Miyaura coupling of aryl bromides with alkylboronic acid.
تواريخ الأحداث: Date Created: 20220606 Latest Revision: 20220623
رمز التحديث: 20240628
DOI: 10.1039/d2cc02161g
PMID: 35667557
قاعدة البيانات: MEDLINE
الوصف
تدمد:1364-548X
DOI:10.1039/d2cc02161g