Inside Back Cover: Visible-Light-Induced Click Chemistry (Angew. Chem. Int. Ed. 35/2015)
An ultrarapid visible-light-driven method for catalyst-free ligation is reported. In their Communication on page10284ff., C. Barner-Kowollik and co-workers describe a highly efficient conjugation between an azirine moiety (white) and diverse dipolarophiles (red) under irradiation from blue LEDs. Fol...
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Published in | Angewandte Chemie International Edition Vol. 54; no. 35; p. 10375 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Weinheim
WILEY-VCH Verlag
24.08.2015
Wiley Subscription Services, Inc |
Edition | International ed. in English |
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Abstract | An ultrarapid visible-light-driven method for catalyst-free ligation is reported. In their Communication on page10284ff., C. Barner-Kowollik and co-workers describe a highly efficient conjugation between an azirine moiety (white) and diverse dipolarophiles (red) under irradiation from blue LEDs. Following the photogeneration of a nitrile ylide (cyan structure), complete conversion into the cycloadduct takes place through a click-type reaction. |
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AbstractList | An ultrarapid visible-light-driven method for catalyst-free ligation is reported. In their Communication on page10284ff., C. Barner-Kowollik and co-workers describe a highly efficient conjugation between an azirine moiety (white) and diverse dipolarophiles (red) under irradiation from blue LEDs. Following the photogeneration of a nitrile ylide (cyan structure), complete conversion into the cycloadduct takes place through a click-type reaction. |
Author | Blinco, James P. Schmidt, Friedrich G. Barner-Kowollik, Christopher Mueller, Jan O. |
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Title | Inside Back Cover: Visible-Light-Induced Click Chemistry (Angew. Chem. Int. Ed. 35/2015) |
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