26067-99-2Relevant articles and documents
Convenient Preparations of Diethyl phosphonates, 2-Azabutadienes, and Isoquinolines from a 1,2-Monoazabisylide Equivalent
Katritzky, Alan R.,Zhang, Guifen,Jiang, Jinlong
, p. 4556 - 4560 (1994)
Diethyl methyl>phosphonate (4), prepared in situ by treatment of 1-methyl>benzotriazole (betmip 6) with diethyl phosphite anion, is converted by treatment with butyllithium into the corresponding carbanion 5.Carbanion 5, the first example of a 1,2-monoazabisylide equivalent, provides a versatile synthetic method to introduce the C=NC=C structural unit, as illustrated by convenient preparations of 1,4-diaryl-2-azabutadienes, 1,1,4,4-tetraaryl-2-azabutadienes, diethyl phosphonates, and isoquinolines.
NICKEL-CATALYZED REACTIONS OF THIAZOLES, ISOXAZOLES, OXAZOLINES AND THIAZOLINES WITH GRIGNARD REAGENTS
Wenkert, Ernest,Han, Aili
, p. 929 - 937 (2007/10/02)
Grignard reagents convert thiazoles, isoxazoles, oxazolines and thiazolines into N-vinylimines, β-amino-α,β-unsaturated ketones, tetrahydrooxazoles and tetrahydrothiazoles, respectively, under the influence of phosphine-ligated nickel species.The reaction characteristics and the uncatalyzed reactions are described.