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- W2089849862 endingPage "12320" @default.
- W2089849862 startingPage "12314" @default.
- W2089849862 abstract "Pyrroloindoline alkaloids constitute a large family of natural products that has inspired the development of an impressive array of new reactions to prepare the key heterocyclic motif. This synopsis will address catalytic, asymmetric reactions developed to synthesize pyrroloindolines bearing C3a all-carbon quaternary stereocenters. The methods described herein include both transition-metal-catalyzed and organocatalyzed reactions that have been demonstrated to be suitable for the synthesis of the pyrroloindoline framework." @default.
- W2089849862 created "2016-06-24" @default.
- W2089849862 creator A5035537769 @default.
- W2089849862 creator A5038661637 @default.
- W2089849862 date "2013-12-02" @default.
- W2089849862 modified "2023-09-27" @default.
- W2089849862 title "Recent Developments in the Catalytic, Asymmetric Construction of Pyrroloindolines Bearing All-Carbon Quaternary Stereocenters" @default.
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- W2089849862 doi "https://doi.org/10.1021/jo4017953" @default.
- W2089849862 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3905788" @default.
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