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BINOL‐Based Chiral Macrocycles and Cages.
- Source :
- Angewandte Chemie International Edition; Jul2024, Vol. 63 Issue 29, p1-14, 14p
- Publication Year :
- 2024
-
Abstract
- Chirality, a fundamental principle in chemistry, biology, and medicine, is prevalent in nature and in organisms. Chiral molecules, such as DNA, RNA, and proteins, are crucial in biomolecular synthesis, as well as in the development of functional materials. Among these, 1,1′‐binaphthyl‐2,2′‐diol (BINOL) stands out for its stable chiral configuration, versatile functionality, and commercial availability. BINOL is widely employed in asymmetric catalysis and chiral materials. This review mainly focuses on recent research over the past five years concerning the use of BINOL derivatives for constructing chiral macrocycles and cages. Their contributions to chiral luminescence, enantiomeric separation, transmembrane transport, and asymmetric catalysis were examined. [ABSTRACT FROM AUTHOR]
- Subjects :
- ENANTIOSELECTIVE catalysis
GLYCOLS
BINAPHTHOL
LUMINESCENCE
ENANTIOMERS
Subjects
Details
- Language :
- English
- ISSN :
- 14337851
- Volume :
- 63
- Issue :
- 29
- Database :
- Complementary Index
- Journal :
- Angewandte Chemie International Edition
- Publication Type :
- Academic Journal
- Accession number :
- 178317084
- Full Text :
- https://doi.org/10.1002/anie.202407034