Enantioselective one-pot synthesis of 2-amino-4H-chromenes via C−H oxidation and Michael addition/ring closure sequences

Chemoselective oxidative generation of ortho-quinone methides and tandem transformations

(2020) Muhammet Uyanik et al.   Nature Chemistry

Enantioselective Organocatalytic Michael Addition and Ring Closure Cascade Reaction of o ‐Quinone Methides with Nitriles

(2020) Jin Wha Park et al.   BULLETIN OF THE KOREAN CHEMICAL SOCIETY

Highly Efficient One‐Pot Three‐Component Synthesis and Antimicrobial Activity of 2‐Amino‐4 H ‐chromene Derivatives

(2019) Ali Aminkhani et al.   JOURNAL OF HETEROCYCLIC CHEMISTRY

Programmable one-pot synthesis of heparin pentasaccharides enabling access to regiodefined sulfate derivatives

(2018) Supriya Dey et al.   Chemical Science

Highly Diastereo- and Enantioselective Organocatalyzed Michael/Oxa-Michael Sequence: Asymmetric Synthesis of Pyranonaphthoquinone Derivatives

(2018) Yong Hwan Kim et al.   BULLETIN OF THE KOREAN CHEMICAL SOCIETY

Catalytic asymmetric substitution of ortho-hydroxybenzyl alcohols with tetronic acid-derived enamines: enantioselective synthesis of tetronic acid-derived diarylmethanes

(2017) Meng-Meng Xu et al.   Organic Chemistry Frontiers

ChiralN,N′-Dioxide-Scandium(III) Complex-Catalyzed Asymmetric Friedel-Crafts Alkylation Reaction ofortho-Hydroxybenzyl Alcohols with C3-Substituted N-Protected Indoles

(2016) Jianfeng Zheng et al.   CHEMISTRY-A EUROPEAN JOURNAL

Discovery of 4-Aryl-4H-Chromenes as Potent Apoptosis Inducers Using a Cell- and Caspase-Based Anti-Cancer Screening Apoptosis Program (ASAP): SAR Studies and the Identification of Novel Vascular Disrupting Agents

(2012) Sui Cai et al.   Anti-Cancer Agents in Medicinal Chemistry