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- W4313532454 abstract "Abstract The preparation of chiral mechanically interlocked molecules has experienced a great development in the last decade, showing a wide range of applications, including catalysis and molecular machinery. New types of chirality have emerged as a consequence of the mechanical bond, such as mechanically planar chirality, which can exist even when both components are achiral. The mechanically planar chirality in such interlocked structures is usually created during the assembly of the rotaxane architecture. Recently, Tian, Zhu and coworkers decoupled the creation of mechanically planar chirality and assembly of the mechanical bond by using a desymmetrizing Suzuki‐Miyaura reaction of a series of mechanically prochiral rotaxanes. This strategy afforded the target chiral interlocked products showing up to 96.5 : 3.5 enantiomeric ratio." @default.
- W4313532454 created "2023-01-06" @default.
- W4313532454 creator A5040134393 @default.
- W4313532454 date "2023-01-01" @default.
- W4313532454 modified "2023-10-02" @default.
- W4313532454 title "Post‐Mechanical Bond Formation Desymmetrization Approach to Obtain Mechanically Planar Chiral Rotaxanes" @default.
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- W4313532454 doi "https://doi.org/10.1002/ajoc.202200601" @default.
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