Rational Design of a Novel Chiral Palladacycle: Synthesis, Optical Resolution, and Stereochemical Evaluation
Author:
Affiliation:
1. Division of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences, Nanyang Technological University, 637371, Singapore
Publisher
Wiley
Subject
Inorganic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejic.200800923
Reference82 articles.
1. For examples see:
2. The first orthopalladation of a primary nitrobenzylamine. Synthesis of chiral cyclopalladated complexes derived from (S)-α-methyl-4-nitrobenzylamine
3. Cyclometallation of 2-phenylaniline and (R)-α-methylbenzylamine by palladium(II) acetate. X-ray molecular structure of [PH2C6H4)C6H4}Br(PPh3)]
4. Synthesis of optically active cyclopalladated complexes of primary benzylamine derivatives, (R)-(−)-2-phenylglycine methyl ester and (±)-1-phenylethylamine
5. Steric Promotion of Aromatic C–H Bond Activation in Primary Benzylamines
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2. Stereocontrol in Preparation of Cyclopalladated Alkylaromatic Oximes and Evaluation of Their Stereoselective Esterase-Type Catalytic Activity;Organometallics;2017-08-18
3. Efficient access to a designed phosphapalladacycle catalyst via enantioselective catalytic asymmetric hydrophosphination;Dalton Transactions;2017
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5. Enantiopurity determination of CN-palladacycles using 31P NMR spectroscopy with (1R,2S,5R)-menthyloxydiphenylphosphine as chiral derivatizing agent;Journal of Organometallic Chemistry;2015-05
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