Asymmetric Transformation of α-Amino Acids Promoted by Optically Active Cobalt(III) Complexes. II.N-Methylalaninatocobalt(III) Complexes with Tetramines
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/53/3/53_3_691/_pdf
Reference20 articles.
1. The Stereospecific Coordination of Sarcosine
2. Crystal structure of diiodo-.DELTA.-R-[bis(ethylenediamine)(N-methyl-S-alaninato)cobalt] and related strain energy minimization calculations
3. Four Isomers of the Bis(ethylenediamine)sarcosinatocobalt(III) Ion: Separation, Identification, and Characterization
4. The stereochemistry of some cobalt(III) triethylenetetramine complexes of glycine and sarcosine
5. Stereospecificity in the [bis(ethylenediamine)-N-methyl-(S)-alaninatecobalt] (2+) and [bis(ethylenediamine)-(S)-prolinatecobalt] (2+) ions
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1. Predetermination of chirality at octahedral centres with tetradentate ligands: prospects for enantioselective catalysis;Coordination Chemistry Reviews;2003-07
2. Prädeterminierte Chiralität an Metallzentren;Angewandte Chemie;1999-02-01
3. Predetermined chirality at metal centers;ANGEW CHEM INT EDIT;1999
4. Efficient stereochemical regulation of octahedral cobalt(III) complexes by a chiral bidentate ligand. Part 1. Effect of N-alkyl substitutions;Journal of the Chemical Society, Dalton Transactions;1994
5. Efficient stereochemical regulation of octahedral cobalt(III) complexes by a chiral bidentate ligand. Part 2. Remarkable effect of the chelate-ring size in the stereoselective formation of sym-cis-(ethylenediamine-N,N′-diacetato)(pentane-2,4-diamine)cobalt(III);J. Chem. Soc., Dalton Trans.;1994
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