Striving to exploit alkyl electrophiles: challenge and choice in transition metal-catalyzed cross-coupling reactions of sulfones

被引:8
|
作者
Liu, Mengli [1 ]
Zheng, Yannan [1 ]
Qiu, Guanyinsheng [1 ,2 ]
Wu, Jie [2 ,3 ]
机构
[1] Jiaxing Univ, Coll Biol Chem Sci & Engn, 118 Jiahang Rd, Jiaxing 314001, Peoples R China
[2] Fudan Univ, Dept Chem, 220 Handan Rd, Shanghai 200433, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, 345 Lingling Rd, Shanghai 200032, Peoples R China
来源
ORGANIC CHEMISTRY FRONTIERS | 2018年 / 5卷 / 17期
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
ALLYLIC GRIGNARD-REAGENTS; QUATERNARY CARBONS; HALIDES; TERTIARY; DERIVATIVES; STEREOCENTERS; ALLYLATION; CENTERS;
D O I
10.1039/c8qo00632f
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
For cross-coupling reactions of alkyl electrophiles, alkyl halides, alkyl tosylates, alkyl acetates and alkyl sulfones exhibit high reaction efficiency when various transition metal catalysts and reaction partners are employed. As crystalline and readily available alkyl electrophiles, alkyl sulfones in radical cross-coupling reactions open a new avenue for modularly generating diverse alkyl compounds. It is believed that more transformations using sulfones as electrophiles will be developed in the near future.
引用
收藏
页码:2615 / 2617
页数:3
相关论文
共 50 条
  • [21] Transition metal-catalyzed alkyl-alkyl bond formation: Another dimension in cross-coupling chemistry
    Choi, Junwon
    Fu, Gregory C.
    SCIENCE, 2017, 356 (6334)
  • [22] Secondary Alkyl Halides in Transition-Metal-Catalyzed Cross-Coupling Reactions
    Rudolph, Alena
    Lautens, Mark
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2009, 48 (15) : 2656 - 2670
  • [23] Secondary alkyl halides in transition-metal-catalyzed cross-coupling reactions
    Davenport Chemistry Laboratories, Department of Chemistry, University of Toronto, 80 St. George Street, Toronto, ON M5S 3H6, Canada
    不详
    Angew. Chem. Int. Ed., 2009, 15 (2656-2670):
  • [24] Transition metal-catalyzed cross-coupling reactions of N-aryl-2-aminopyridines
    Doraghi, Fatemeh
    Rezainia, Lina
    Morshedsolouk, Mohammad Hossein
    Navid, Hamed
    Larijani, Bagher
    Mahdavi, Mohammad
    RSC ADVANCES, 2025, 15 (02) : 1134 - 1151
  • [25] Stereocontrolled synthesis of lissoclinolide by sequential transition metal-catalyzed lactonization/cross-coupling reactions
    Rossi, R
    Bellina, F
    Biagetti, M
    Mannina, L
    TETRAHEDRON LETTERS, 1998, 39 (42) : 7799 - 7802
  • [26] Secondary phosphine oxides: Versatile ligands in transition metal-catalyzed cross-coupling reactions
    Shaikh, Tanveer Mahamadali
    Weng, Chia-Ming
    Hong, Fung-E
    COORDINATION CHEMISTRY REVIEWS, 2012, 256 (9-10) : 771 - 803
  • [27] Progress on the Transition Metal-catalyzed Cross-coupling Reaction of Thioesters
    Han Mingliang
    Xu Lihua
    ACTA CHIMICA SINICA, 2023, 81 (04) : 381 - 392
  • [28] Metal-Catalyzed Cross-Coupling Reactions on Azaindole Synthesis and Functionalization
    Sofia Santos, A.
    Mortinho, Ana C.
    Marques, M. Manuel B.
    MOLECULES, 2018, 23 (10):
  • [29] Progress of transition metal-catalyzed cross-coupling mediated by PyBroP
    Chen, Guojun
    Du, Jianshi
    CHINESE SCIENCE BULLETIN, 2014, 59 (17): : 1942 - 1949
  • [30] Progress of transition metal-catalyzed cross-coupling mediated by PyBroP
    Guojun Chen
    Jianshi Du
    Chinese Science Bulletin, 2014, 59 (17) : 1942 - 1949