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Enantioselective Organozinc Addition to Aldehydes Using Planar Chiral [2.2]Paracyclophane‐Imidazoline N,O‐Ligands.
- Source :
-
Chemistry - A European Journal . Oct2024, p1. 10p. 8 Illustrations. - Publication Year :
- 2024
-
Abstract
- We present an improved and convenient synthesis of [2.2]paracyclophane‐imidazoline N,O‐ligands with central and planar chirality in seven steps starting from [2.2]paracyclophane. The utility of these ligands in organozinc additions to aldehydes is described. The asymmetric ethylation of aldehydes proceeded with enantioselectivities of up to 97 % ee, while the asymmetric arylation of aldehydes gave up to 95 % ee (<italic>R</italic>) and 82 % ee (<italic>S</italic>) using (<italic>S</italic>,<italic>S</italic>,<italic>S</italic>P)‐UCD‐Imphanol and (<italic>S</italic>,<italic>S</italic>,<italic>R</italic>P)‐UCD‐Imphanol, respectively. [ABSTRACT FROM AUTHOR]
- Subjects :
- *PLANAR chirality
*ETHYLATION
*LIGANDS (Chemistry)
*ARYLATION
*IMIDAZOLINES
Subjects
Details
- Language :
- English
- ISSN :
- 09476539
- Database :
- Academic Search Index
- Journal :
- Chemistry - A European Journal
- Publication Type :
- Academic Journal
- Accession number :
- 180794381
- Full Text :
- https://doi.org/10.1002/chem.202403345