Journal article

Authors list: Ahles, S; Ruhl, J; Strauss, MA; Wegner, HA

Publication year: 2019

Pages: 3927-3930

Journal: Organic Letters

Volume number: 21

Issue number: 11

ISSN: 1523-7060

eISSN: 1523-7052

Open access status: Bronze

DOI Link: https://doi.org/10.1021/acs.orglett.9b01020

Publisher: American Chemical Society

Abstract: 
A bidentate Lewis acid catalyzed domino inverse-electron-demand Diels-Alder reaction combined with a photoinduced ring opening formally inserts o-xylene moieties into enamine double bonds. After reduction, phenethylamines were obtained in good yields. The scope of the reaction was determined by variation of all three starting compounds: phthalazines, aldehydes, and amines.

Harvard Citation style: Ahles, S., Ruhl, J., Strauss, M. and Wegner, H. (2019) Combining Bidentate Lewis Acid Catalysis and Photochemistry: Formal Insertion of o-Xylene into an Enamine Double Bond, Organic Letters, 21(11), pp. 3927-3930. https://doi.org/10.1021/acs.orglett.9b01020

APA Citation style: Ahles, S., Ruhl, J., Strauss, M., & Wegner, H. (2019). Combining Bidentate Lewis Acid Catalysis and Photochemistry: Formal Insertion of o-Xylene into an Enamine Double Bond. Organic Letters. 21(11), 3927-3930. https://doi.org/10.1021/acs.orglett.9b01020