27185-57-5Relevant articles and documents
Pd(II)-Catalyzed Aerobic Intermolecular 1,2-Diamination of Conjugated Dienes: A Regio- and Chemoselective [4 + 2] Annulation for the Synthesis of Tetrahydroquinoxalines
Wu, Zhengxing,Wen, Ke,Zhang, Jingang,Zhang, Wanbin
supporting information, p. 2813 - 2816 (2017/06/07)
A Pd(II)-catalyzed aerobic intermolecular 1,2-diamination of conjugated dienes was developed for the regio- and chemoselective preparation of a variety of functionalized tetrahydroquinoxalines, using simple sulfonyl protected o-phenylendiamines as a nitrogen source. This methodology provides a direct and efficient synthesis of tetrahydroquinoxalines. O2 was used as the stoichiometric oxidant, and reaction conditions were applied to a series of o-phenylendiamines and conjugated dienes. 35 examples are described, and good yields and selectivities are obtained for the majority of the products.
THE MENKE REACTION WITH DISULFONYL DERIVATIVES OF PHENYLENEDIAMINES
Zakatov, V. V.,Dubina, V. L.,Bezverkhii, N. P.,Cheremisinov, I. V.,Nevidomskaya, G. S.
, p. 1808 - 1809 (2007/10/02)
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