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Novel O,N,N,O-tetradentate ligand from tartaric acid
- Source :
- Tetrahedron. 69:6162-6169
- Publication Year :
- 2013
- Publisher :
- Elsevier BV, 2013.
-
Abstract
- A new class of highly stable O,N,N,O-tetradentate bioxazoline ligands were synthesized from l-tartaric acid. Exploration of those ligands in Pd-catalyzed asymmetric allylic alkylation yielded alkylated product up to 96% ee. Necessity of additional chelation to obtain high enantioselectivity was also demonstrated. Structural modifications of this ligand might result in identification of a novel privileged chiral ligand from an inexpensive chiral pool. � 2013 Elsevier Ltd. All rights reserved.
- Subjects :
- dimethyl 2 [1,3 bis(4 methoxyphenyl)allyl]malonate
chirality
o,n,n,o tetradentate bioxazoline ligand
Alkylation
proton nuclear magnetic resonance
Biochemistry
Tsuji–Trost reaction
chemistry.chemical_compound
chelation
2 [1,3 bis(4 chlorophenyl)allyl]malononitrile
dimethyl 2 [1,3 bis(3 chlorophenyl)allyl]malonate
Drug Discovery
Chemistry
Chiral ligand
dimethyl 2 [1,3 bis(4 fluorophenyl)allyl]malonate
dimethyl 2 [1,3 bis(4 bromophenyl)allyl]malonate
unclassified drug
priority journal
Tartaric acid
hydrogenation
chemical modification
crystal structure
Stereochemistry
dimethyl 2 (4 phenylbut 3 en 2 yl)malonate
asymmetric allylic alkylation
complex formation
enantioselectivity
Chelation
dimethyl 2 (1,3 diphenylallyl)malonate
alkylation
diethyl 2 [1,3 bis(4-chlorophenyl)allyl]malonate
oxazoline derivative
solvent effect
catalysis
dimethyl 2 [1,3 bis(4 chlorophenyl)allyl]malonate
Ligand
organic chemicals
Organic Chemistry
Enantioselective synthesis
diethyl 2 [1,3 bis(4 chlorophenyl)allyl]malonate
dimethyl 2 (1,3 dip tolylallyl)malonate
carbon nuclear magnetic resonance
palladium
dimethyl 2 [1,3 di(naphthalen 2 yl)allyl]malonate
tartaric acid
substitution reaction
chemical structure
dimethyl 2 [1,3 bis(3 bromophenyl)allyl]malonate
3 [1,3 bis(4 chlorophenyl)allyl]pentane 2,4 dione
Tetradentate ligand
Subjects
Details
- ISSN :
- 00404020
- Volume :
- 69
- Database :
- OpenAIRE
- Journal :
- Tetrahedron
- Accession number :
- edsair.doi.dedup.....8c6660c62b59849fef66d125183e779a
- Full Text :
- https://doi.org/10.1016/j.tet.2013.05.049