Matches in SemOpenAlex for { <https://semopenalex.org/work/W4220768081> ?p ?o ?g. }
- W4220768081 abstract "Abstract Molecular capsules enable the conversion of substrates inside a closed cavity, mimicking to some extent enzymatic catalysis. Chirality transfer from the molecular capsule onto the encapsulated substrate has been only studied in a few cases. Here we demonstrate that chirality transfer is possible inside a rather large molecular container of approximately 1400 Å 3 . Specifically, we present 1) the first examples of optically active hexameric resorcin[4]arene capsules, 2) their ability to enantioselectively catalyze tail‐to‐head terpene cyclizations, and 3) the surprisingly high sensitivity of enantioselectivity on the structural modifications." @default.
- W4220768081 created "2022-04-03" @default.
- W4220768081 creator A5052177438 @default.
- W4220768081 creator A5080938855 @default.
- W4220768081 creator A5084661514 @default.
- W4220768081 date "2022-04-22" @default.
- W4220768081 modified "2023-10-09" @default.
- W4220768081 title "Enantioselective Tail‐to‐Head Terpene Cyclizations by Optically Active Hexameric Resorcin[4]arene Capsule Derivatives" @default.
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- W4220768081 doi "https://doi.org/10.1002/anie.202203384" @default.
- W4220768081 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/35324038" @default.
- W4220768081 hasPublicationYear "2022" @default.
- W4220768081 type Work @default.
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