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Leijie Zhou

Researcher at China Agricultural University

Publications -  43
Citations -  1027

Leijie Zhou is an academic researcher from China Agricultural University. The author has contributed to research in topics: Annulation & Catalysis. The author has an hindex of 17, co-authored 40 publications receiving 789 citations.

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Enantioselective Synthesis of Chiral Medium-Sized Cyclic Compounds via Tandem Cycloaddition/Cope Rearrangement Strategy

TL;DR: Under mild conditions, palladium-catalyzed asymmetric tandem reaction of various substituted VECs and coumalates or pyrones proceeds smoothly to produce the corresponding medium-sized heterocyclic compounds in high yields with very high enantioselectivities.
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Formal [5+3] Cycloaddition of Zwitterionic Allylpalladium Intermediates with Azomethine Imines for Construction of N,O-Containing Eight-Membered Heterocycles

TL;DR: In this paper, a formal cycloaddition of zwitterionic allylpalladium intermediates with 1,3-dipoles was developed, providing N,O-containing eight-membered heterocyclic compounds in high yields.
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Phosphine-Catalyzed Enantioselective [4 + 3] Annulation of Allenoates with C,N-Cyclic Azomethine Imines: Synthesis of Quinazoline-Based Tricyclic Heterocycles

TL;DR: The first catalytic enantioselective [4 + 3] annulation of allenoates with C,N-cyclic azomethine imines is developed, which works efficiently under mild reaction conditions to afford seven-membered ring-fused quinazoline-based tricyclic heterocycles in high yields with good to excellent diastereo- and enantiOSElectivities.
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Phosphine-Catalyzed [2 + 4] Annulation of Allenoates with Thiazolone-Derived Alkenes: Synthesis of Functionalized 6,7-Dihydro-5H-pyrano[2,3-d]thiazoles

TL;DR: Phosphine-catalyzed [2 + 4] annulation of allenoates with thiazolone-derived alkenes has been achieved under mild conditions, giving biologically important 6,7-dihydro-5H-pyrano[2,3-d]thiazole derivatives in high to excellent yields.
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Enantioselective Construction of Tetrahydroquinazoline Motifs via Palladium-Catalyzed [4 + 2] Cycloaddition of Vinyl Benzoxazinones with Sulfamate-Derived Cyclic Imines.

TL;DR: This reaction represents the first Pd-catalyzed asymmetric decarboxylative cycloaddition of vinyl benzoxazinones with imines, affording the tetrahydroquinazolines bearing several functional rings in high yields with good to excellent diastereoselectivities and excellent enantioselectivity.