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• W2012113025 endingPage "2922" @default.
• W2012113025 startingPage "2916" @default.
• W2012113025 abstract "Abstract We report a full account of our work towards the development of Mo‐catalyzed asymmetric allylic alkylation reactions with 3‐alkyloxindoles as nucleophiles. The reaction is complementary to the Pd‐catalyzed reaction with regard to the scope of oxindole nucleophiles. A number of 3‐alkyloxindoles were alkylated successfully under mild conditions to give products with excellent yields and good‐to‐excellent enantioselectivities. Applications of this method to the preparation of indoline alkaloids such as (−)‐physostigmine, ent‐ (−)‐debromoflustramine B, and the indolinoquinoline rings of communesin B are reported." @default.
• W2012113025 created "2016-06-24" @default.
• W2012113025 creator A5032412691 @default.
• W2012113025 creator A5075500520 @default.
• W2012113025 date "2011-02-02" @default.
• W2012113025 modified "2023-10-18" @default.
• W2012113025 title "Molybdenum-Catalyzed Asymmetric Allylic Alkylation of 3-Alkyloxindoles: Reaction Development and Applications" @default.
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• W2012113025 doi "https://doi.org/10.1002/chem.201002569" @default.
• W2012113025 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3714863" @default.
• W2012113025 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/21290436" @default.
• W2012113025 hasPublicationYear "2011" @default.
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