Solvent-Free Microwave Promoted [3+2] Cycloaddition of Alkyne-Azide in Uniform CuO Hollow Nanospheres

被引:21
|
作者
Kang, Hyuntae [1 ,3 ]
Lee, Hyun Ju [1 ,3 ]
Park, Ji Chan [2 ]
Song, Hyunjoon [2 ]
Park, Kang Hyun [1 ,3 ]
机构
[1] Pusan Natl Univ, Dept Chem, Pusan 609735, South Korea
[2] Korea Adv Inst Sci & Technol, Dept Chem, Taejon 305701, South Korea
[3] Pusan Natl Univ, Chem Inst Funct Mat, Pusan 609735, South Korea
关键词
Microwave; Copper oxide; Acetylene black; Heterogeneous; Catalyst; Click reaction; NANOSTRUCTURES; CHEMISTRY; CU2O;
D O I
10.1007/s11244-010-9481-0
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
CuO hollow nanospheres on acetylene black (CuO/AB) have been used for the catalytic [3 + 2] cycloaddition of azides with terminal alkynes without solvent, and within 1 min under microwave irradiation. The CuO/AB was readily separated by centrifugation, and could be reused five times under the present reaction conditions without any loss of catalytic activity.
引用
收藏
页码:523 / 528
页数:6
相关论文
共 50 条
  • [1] Solvent-Free Microwave Promoted [3 + 2] Cycloaddition of Alkyne-Azide in Uniform CuO Hollow Nanospheres
    Hyuntae Kang
    Hyun Ju Lee
    Ji Chan Park
    Hyunjoon Song
    Kang Hyun Park
    Topics in Catalysis, 2010, 53 : 523 - 528
  • [2] Immobilized CuO Hollow Nanospheres Catalyzed Alkyne-Azide Cycloadditions
    Kang, Hyuntae
    Jung, Hyun Seok
    Kim, Jee Young
    Park, Ji Chan
    Kim, Mijong
    Song, Hyunjoon
    Park, Kang Hyun
    JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY, 2010, 10 (10) : 6504 - 6509
  • [3] Azide-Alkyne Huisgen [3+2] Cycloaddition Using CuO Nanoparticles
    Woo, Hyunje
    Kang, Hyuntae
    Kim, Aram
    Jang, Seongwan
    Park, Ji Chan
    Park, Sungkyun
    Kim, Byeong-Su
    Song, Hyunjoon
    Park, Kang Hyun
    MOLECULES, 2012, 17 (11): : 13235 - 13252
  • [4] Injectable biocompatible poly(2-oxazoline) hydrogels by strain promoted alkyne-azide cycloaddition
    Park, Jong-Ryul
    Bolle, Eleonore C. L.
    Cavalcanti, Amanda Dos Santos
    Podevyn, Annelore
    Van Guyse, Joachim F. R.
    Forget, Aurelien
    Hoogenboom, Richard
    Dargaville, Tim R.
    BIOINTERPHASES, 2021, 16 (01)
  • [5] Achievements in the synthesis of cyclooctynes for ring strain-promoted [3+2] azide-alkyne cycloaddition
    Chupakhin, Evgeny G.
    Krasavin, Mikhail Yu.
    CHEMISTRY OF HETEROCYCLIC COMPOUNDS, 2018, 54 (05) : 483 - 501
  • [6] Achievements in the synthesis of cyclooctynes for ring strain-promoted [3+2] azide-alkyne cycloaddition
    Evgeny G. Chupakhin
    Mikhail Yu. Krasavin
    Chemistry of Heterocyclic Compounds, 2018, 54 : 483 - 501
  • [7] A strain-promoted [3+2] azide-alkyne cycloaddition for covalent modification of blomolecules in living systems
    Agard, NJ
    Prescher, JA
    Bertozzi, CR
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (46) : 15046 - 15047
  • [8] Solvent-Free Copper-Catalyzed Azide-Alkyne Cycloaddition under Mechanochemical Activation
    Rinaldi, Laura
    Martina, Katia
    Baricco, Francesca
    Rotolo, Laura
    Cravotto, Giancarlo
    MOLECULES, 2015, 20 (02) : 2837 - 2849
  • [9] Fast copper-free click DNA ligation by the ring-strain promoted alkyne-azide cycloaddition reaction
    Shelbourne, Montserrat
    Chen, Xiong
    Brown, Tom
    El-Sagheer, Afaf H.
    CHEMICAL COMMUNICATIONS, 2011, 47 (22) : 6257 - 6259
  • [10] Metal-Free 1,5-Regioselective Azide-Alkyne [3+2]-Cycloaddition
    Kloss, Florian
    Koehn, Uwe
    Jahn, Burkhard O.
    Hager, Martin D.
    Goerls, Helmar
    Schubert, Ulrich S.
    CHEMISTRY-AN ASIAN JOURNAL, 2011, 6 (10) : 2816 - 2824