wang.scbb pkusz.edu.cn

Wang Laboratory

Visible-Light-Promoted Vinylation of Tetra. Gold-Catalyzed Rearrangement of Alkynyl Do. Asymmetric Synthesis of the Tricyclic Core. Asymmetric synthesis of the 5 6 7 tricyclic system common to theCalyciphyllineA-type alkaloids is reported, featuring Overman rearrangement, Heck cyclization, intram. Remarkable Ag-carbenoid-initiated enone cyclopropanation hydrolytic fragmentation. Visible-light photo-catalytic C-C bond cle. Chirality Helicity Conservation of Electronic Helicity.

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Wang Laboratory

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Visible-Light-Promoted Vinylation of Tetra. Gold-Catalyzed Rearrangement of Alkynyl Do. Asymmetric Synthesis of the Tricyclic Core. Asymmetric synthesis of the 5 6 7 tricyclic system common to theCalyciphyllineA-type alkaloids is reported, featuring Overman rearrangement, Heck cyclization, intram. Remarkable Ag-carbenoid-initiated enone cyclopropanation hydrolytic fragmentation. Visible-light photo-catalytic C-C bond cle. Chirality Helicity Conservation of Electronic Helicity.

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The site wang.scbb.pkusz.edu.cn states the following, "Gold-Catalyzed Rearrangement of Alkynyl Do." We noticed that the webpage said " Asymmetric Synthesis of the Tricyclic Core." It also stated " Asymmetric synthesis of the 5 6 7 tricyclic system common to theCalyciphyllineA-type alkaloids is reported, featuring Overman rearrangement, Heck cyclization, intram. Remarkable Ag-carbenoid-initiated enone cyclopropanation hydrolytic fragmentation. Visible-light photo-catalytic C-C bond cle. Chirality Helicity Conservation of Electronic Helicity."

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