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![Scope and Mechanistic Analysis of the Enantioselective Synthesis of Allenes by Rhodium-Catalyzed Tandem Ylide Formation/[2,3]-Sigmatropic Rearrangement between Donor/Acceptor Carbenoids and Propargylic Alcohols | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/ja3061529/asset/images/ja3061529.social.jpeg_v03 "Scope and Mechanistic Analysis of the Enantioselective Synthesis of Allenes by Rhodium-Catalyzed Tandem Ylide Formation/[2,3]-Sigmatropic Rearrangement between Donor/Acceptor Carbenoids and Propargylic Alcohols | Journal of the American Chemical Society")
Scope and Mechanistic Analysis of the Enantioselective Synthesis of Allenes by Rhodium-Catalyzed Tandem Ylide Formation/[2,3]-Sigmatropic Rearrangement between Donor/Acceptor Carbenoids and Propargylic Alcohols | Journal of the American Chemical Society
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Visible‐Light‐Induced C−H Functionalization and C−C/C−X Bond‐Forming Oxidative Cross‐Coupling Reactions - Zhang - 2018 - Asian Journal of Organic Chemistry - Wiley Online Library
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Advanced Functional Materials: Vol 31, No 30
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Molecules | Free Full-Text | Dihydroxyquingdainone Induces Apoptosis in Leukaemia and Lymphoma Cells via the Mitochondrial Pathway in a Bcl-2- and Caspase-3-Dependent Manner and Overcomes Resistance to Cytostatic Drugs In Vitro
