Nitrile Oxide Cycloaddition

Nitrile Oxide Cycloaddition is a bioorthogonal reaction that belongs to the class of 1,3-dipolar cycloadditions, distinguished by the selective and catalyst-free formation of isoxazoline adducts through the interaction of a nitrile oxide dipole with a dipolarophilic alkene or alkyne under physiological conditions.

837

Publications

28.4K

Citations

2.3K

Authors

605

Institutions

Publications per year

2017–2026

87

Authors

2.3K

  1. SK
    Shuji Kanemasa

    Kyushu University, Japan

    22 publications · 1K citations

    18

    h-index

  2. PC
    Pierluigi Caramella

    University of Pavia, Italy

    15 publications · 518 citations

    14

    h-index

  3. KN
    K. N. Houk

    University of California, Los Angeles, United States

    14 publications · 968 citations

    14

    h-index

  4. MJ
    Mark J. Kurth

    University of California, Davis, United States

    14 publications · 326 citations

    13

    h-index

  5. EM
    Erick M. Carreira

    ETH Zurich, Switzerland

    13 publications · 766 citations

    12

    h-index

1–5 of 2.3K

Venues

  1. The Journal of Organic Chemistry

    JOC · 90 publications · 4K citations

    37

    h-index

  2. Tetrahedron Letters

    96 publications · 2.6K citations

    30

    h-index

  3. Organic Letters

    OL · 44 publications · 2.3K citations

    29

    h-index

  4. Tetrahedron

    69 publications · 1.9K citations

    28

    h-index

  5. Journal of the American Chemical Society

    JACS · 21 publications · 3.7K citations

    20

    h-index

1–5