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Showing posts with the label Propargyl

Azepine Synthesis from Alkyl Azide and Propargylic Ester

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JOC Azepine Synthesis from Alkyl Azide and Propargylic Ester via Gold Catalysis Heng Liu, Xin Li, Zili Chen, and Wen-Xiang Hu

Cycloaddition/Hydrolytic Michael Addition/Retro-Aldol Reactions of Propargylic Esters

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Angewchem Gold-Catalyzed [3+2] Cycloaddition/Hydrolytic Michael Addition/Retro-Aldol Reactions of Propargylic Esters Tethered to Cyclohexadienones Shunyou Cai, Zheng Liu, Weibin Zhang, Xinyang Zhao and Prof. David Zhigang Wang

Dynamic Kinetic Asymmetric Transformation of Propargyl Esters

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Jacs Chiral (Acyclic Diaminocarbene)Gold(I)-Catalyzed Dynamic Kinetic Asymmetric Transformation of Propargyl Esters Yi-Ming Wang, Christian N. Kuzniewski, Vivek Rauniyar, Christina Hoong, and F. Dean Toste

General Procedure for the Synthesis of Enones via Gold-Catalyzed Meyer−Schuster Rearrangement

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JOC A General Procedure for the Synthesis of Enones via Gold-Catalyzed Meyer−Schuster Rearrangement of Propargylic Alcohols at Room Temperature Matthew N. Pennell, Matthew G. Unthank, Peter Turner, and Tom D. Sheppard