95730-58-8Relevant articles and documents
Synthesis of β-prolinols via [3+2] cycloaddition and one-pot programmed reduction: Valuable building blocks for polyheterocycles
Li, Jundong,Lin, Na,Yu, Lei,Zhang, Yandong
supporting information, p. 5777 - 5780 (2016/12/06)
A novel two-step synthesis of multisubstituted β-prolinols has been developed, featuring a [3+2] cycloaddition of azomethine ylides and a programmed reduction triggered by the combination of borane and lithium aluminum hydride (LAH). β-Prolinols are shown to be valuable building blocks for polyheterocycles.
2-Aryl-1,9-dihydrochromeno[3,2-d]imidazoles: A facile synthesis from salicylaldehydes and arylideneaminoacetonitrile
Costa, Marta,Proena, Fernanda
experimental part, p. 1799 - 1804 (2011/04/16)
2-Aryl-1,9-dihydrochromeno[3,2-d]imidazoles were prepared by a one-pot cascade reaction involving salicylaldehydes and arylideneaminoacetonitriles. These novel compounds were isolated in 11-95% yield after reflux in ethanol and triethylamine. A dimeric st