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An expeditious FeCl<sub>3</sub>-catalyzed cascade 1,4-conjugate addition/annulation/1,5-H shift sequence for modular access of all-pyrano-moiety-substituted chromenes

Xinwei He, Ruxue Li, Pui Ying Choy, Jiahui Duan, Zhenzhen Yin, Keke Xu, Qiang Tang, Rong‐Lin Zhong, Yongjia Shang, Fuk Yee Kwong

2022Chemical Science24 citationsDOIOpen Access PDF

Abstract

, and particularly under undried acetonitrile and air atmosphere conditions. This method exhibits a broad substrate scope and displays nice functional group compatibility, thus providing an efficient access of 3,4-disubstituted iminochromenes.

Topics & Concepts

SynthonAnnulationAromatizationChemistryMoietyRegioselectivityCombinatorial chemistryCatalysisCycloadditionConjugateAcetonitrileArylMedicinal chemistryStereochemistryOrganic chemistryMathematicsAlkylMathematical analysisSynthesis of Indole DerivativesCatalytic C–H Functionalization MethodsSulfur-Based Synthesis Techniques
An expeditious FeCl<sub>3</sub>-catalyzed cascade 1,4-conjugate addition/annulation/1,5-H shift sequence for modular access of all-pyrano-moiety-substituted chromenes | Litcius