Journalartikel
Autorenliste: Kessler, SN; Wegner, HA
Jahr der Veröffentlichung: 2012
Seiten: 3268-3271
Zeitschrift: Organic Letters
Bandnummer: 14
Heftnummer: 13
ISSN: 1523-7060
DOI Link: https://doi.org/10.1021/ol301167q
Verlag: American Chemical Society
Abstract:
A new one-pot strategy for the synthesis of phthalazines and pyridazino-aromatics starting from aromatic aldehydes has been developed. A variety of substituents ranging from electron withdrawing to donating is tolerated furnishing the desired 1,2-diazine in good to excellent yields. The products have been applied to the bidentate Lewis acid catalyzed inverse electron-demand Diels-Alder (IEDDA) reaction opening a novel two-step entry into substituted naphthalenes, such as Naproxen.
Zitierstile
Harvard-Zitierstil: Kessler, S. and Wegner, H. (2012) One-Pot Synthesis of Phthalazines and Pyridazino-aromatics: A Novel Strategy for Substituted Naphthalenes, Organic Letters, 14(13), pp. 3268-3271. https://doi.org/10.1021/ol301167q
APA-Zitierstil: Kessler, S., & Wegner, H. (2012). One-Pot Synthesis of Phthalazines and Pyridazino-aromatics: A Novel Strategy for Substituted Naphthalenes. Organic Letters. 14(13), 3268-3271. https://doi.org/10.1021/ol301167q