Recent Advances in Transition-Metal-Catalyzed Sonogashira Cross-Coupling Reactions of Alkyl Electrophiles
出版年份 2023 全文链接
标题
Recent Advances in Transition-Metal-Catalyzed Sonogashira Cross-Coupling Reactions of Alkyl Electrophiles
作者
关键词
-
出版物
SYNTHESIS-STUTTGART
Volume -, Issue -, Pages -
出版商
Georg Thieme Verlag KG
发表日期
2023-11-03
DOI
10.1055/s-0042-1751506
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Photoinduced Copper-Catalyzed Monofluoroalkylation of Terminal Alkynes to Propargylic Fluorides
- (2023) Duo-Duo Hu et al. Organic Letters
- Diversified Synthesis of All-Carbon Quaternary gem-Difluorinated Cyclopropanes via Copper-Catalyzed Cross-Coupling
- (2023) Bin Li et al. Organic Letters
- Aryl Radical Enabled, Copper-Catalyzed Sonogashira-Type Cross-Coupling of Alkynes with Alkyl Iodides
- (2023) Xiaojun Zeng et al. ACS Catalysis
- Cu(I)/N,N-Imine Ligand Catalyzed C(sp3)–C(sp) Coupling of Alkyl Bromides with Alkynes: Scope and Mechanistic Investigation
- (2023) Swati Jain et al. ORGANIC LETTERS
- Development of Novel Phosphino‐Oxazoline Ligands and Their Application in Asymmetric Alkynlylation of Benzylic Halides
- (2022) Rui Guo et al. CHINESE JOURNAL OF CHEMISTRY
- Mechanism-based ligand design for copper-catalysed enantioconvergent C(sp3)–C(sp) cross-coupling of tertiary electrophiles with alkynes
- (2022) Fu-Li Wang et al. Nature Chemistry
- Tetrasubstituted Carbon Stereocenters via Copper-Catalyzed Asymmetric Sonogashira Coupling Reactions with Cyclic gem-Dihaloketones and Tertiary α-Carbonyl Bromides
- (2022) Xueling Mo et al. ACS Catalysis
- Carboxamide-Directed Stereospecific Couplings of Chiral Tertiary Alkyl Halides with Terminal Alkynes
- (2022) Hiroki Akagawa et al. ACS Catalysis
- Nickel-Catalyzed Sonogashira Coupling Reactions of Nonactivated Alkyl Chlorides under Mild Conditions
- (2021) Qingqing Fan et al. ORGANOMETALLICS
- Copper-Catalyzed Asymmetric Deconstructive Alkynylation of Cyclic Oximes
- (2021) Hang-Dong Zuo et al. ACS Catalysis
- Nickel-catalyzed deaminative Sonogashira coupling of alkylpyridinium salts enabled by NN2 pincer ligand
- (2021) Xingjie Zhang et al. Nature Communications
- Mechanisms of Nickel-Catalyzed Coupling Reactions and Applications in Alkene Functionalization
- (2020) Justin Diccianni et al. ACCOUNTS OF CHEMICAL RESEARCH
- A Copper‐Catalyzed Sonogashira Coupling Reaction of Diverse Activated Alkyl Halides with Terminal Alkynes Under Ambient Conditions
- (2020) Yu‐Xi Cao et al. ADVANCED SYNTHESIS & CATALYSIS
- Copper‐Catalyzed Enantioselective Sonogashira Type Coupling of Alkynes with α‐Bromoamides
- (2020) Xueling Mo et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- A general asymmetric copper-catalysed Sonogashira C(sp3)–C(sp) coupling
- (2019) Xiao-Yang Dong et al. Nature Chemistry
- Photoinduced Copper-Catalyzed Coupling of Terminal Alkynes and Alkyl Iodides
- (2018) Avijit Hazra et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Sonogashira reactions of alkyl halides catalyzed by NHC [CNN] pincer nickel(ii) complexes
- (2018) Zijing Wang et al. NEW JOURNAL OF CHEMISTRY
- Copper-Catalyzed Functionalized Tertiary-Alkylative Sonogashira Type Couplings via Copper Acetylide at Room Temperature
- (2017) Yu Yamane et al. ACS Catalysis
- Cu-Catalyzed Alkynylation of Unactivated C(sp3)–X Bonds with Terminal Alkynes through Directing Strategy
- (2016) Fei-Xian Luo et al. ORGANIC LETTERS
- Nickel-Catalyzed Direct Alkylation of Terminal Alkynes at Room Temperature: A Hemilabile Pincer Ligand Enhances Catalytic Activity
- (2015) Pablo M. Pérez García et al. ACS Catalysis
- Nickel-Catalyzed Sonogashira Reactions of Non-activated Secondary Alkyl Bromides and Iodides
- (2013) Jun Yi et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Ni-Catalyzed Sonogashira Coupling of Nonactivated Alkyl Halides: Orthogonal Functionalization of Alkyl Iodides, Bromides, and Chlorides
- (2009) Oleg Vechorkin et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Create your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create NowAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started