Triethyl Phosphite Mediated Domino Reaction: Direct Conversion of ω‐Nitroalkenes Into N‐Heterocycles | Zendy

Merişor Elena | Zendy; Conrad Jürgen | Zendy; Klaiber Iris | Zendy; Mika Sabine | Zendy; Beifuss Uwe | Zendy

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Triethyl Phosphite Mediated Domino Reaction: Direct Conversion of ω‐Nitroalkenes Into N‐Heterocycles

Author(s) -

Merişor Elena,

Conrad Jürgen,

Klaiber Iris,

Mika Sabine,

Beifuss Uwe

Publication year - 2007

Publication title -

angewandte chemie international edition

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 5.831

H-Index - 550

eISSN - 1521-3773

pISSN - 1433-7851

DOI - 10.1002/anie.200605260

Subject(s) - domino , microwave irradiation , chemistry , domino effect , reaction conditions , combinatorial chemistry , organic chemistry , catalysis , physics , nuclear physics

Dominos on cycles : Several N‐heterocycles, such as 3,4‐dihydro‐2 H ‐1,4‐benzoxazines, 1,2,3,4‐tetrahydroquinoxalines, and 1,2,3,4‐tetrahydroquinolines, can be obtained through a novel domino reaction mediated by triethyl phosphite under the influence of microwave irradiation (MW) in a single step from nitroaromatic compounds (see scheme).

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