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• W2753156614 endingPage "12966" @default.
• W2753156614 startingPage "12960" @default.
• W2753156614 abstract "The fundamental role that aldol chemistry adopts in various disciplines, such as stereoselective catalysis or the biosynthesis of aromatic polyketides, illustrates its exceptional versatility. On the one hand, numerous aldol addition reactions reliably transfer the stereochemical information from catalysts into various valuable products. On the other hand, countless aromatic polyketide natural products are produced by an ingenious biosynthetic machinery based on arene-forming aldol condensations. With the aim of complementing aldol methodology that controls stereocenter configuration, we recently combined these two tenets by investigating small-molecule-catalyzed aldol condensation reactions that stereoselectively form diverse axially chiral compounds through the construction of a new aromatic ring." @default.
• W2753156614 created "2017-09-15" @default.
• W2753156614 creator A5008910219 @default.
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• W2753156614 date "2017-09-05" @default.
• W2753156614 modified "2023-09-25" @default.
• W2753156614 title "Stereoselective Arene‐Forming Aldol Condensation: Catalyst‐Controlled Synthesis of Axially Chiral Compounds" @default.
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• W2753156614 doi "https://doi.org/10.1002/chem.201702471" @default.
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• W2753156614 hasPublicationYear "2017" @default.
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