2011
DOI: 10.1007/s12039-011-0093-4
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Palladium catalysed asymmetric alkylation of benzophenone Schiff base glycine esters in ionic liquids

Abstract: Asymmetric alkyl substitution of various benzophenone Schiff base substrates under biphasic conditions proceeded using optically active Palladium(II) complexes. The corresponding products were obtained in high yields but with moderate enantiomeric excess (ee). Addition of specific ionic liquids to the reaction medium enhanced reactivity and selectivity for phase transfer catalytic (PTC) glycine alkylation. It has been found that there is an anionic influence of the ionic liquids that modify the steric environm… Show more

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Cited by 4 publications
(1 citation statement)
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“…Their often unique property profiles are extremely low volatility, good thermal stability, wide liquid temperature range, nonflammability, good dissolving ability, low viscosity, negligible vapor pressure, and high ionic conductivity. [21][22][23][24][25][26][27][28][29] The aim of this study is the use of natural amino acid building blocks for efficient synthesis of novel biodegradable and chiral nanostructured PAIs, using molten tetrabutylammonium bromide (TBAB) as green medium. PAIs with main-chain chirality were synthesized via direct step-growth polymerization reaction of different chiral diacids (4a-4d) with 4,4′-methylenebis(3-chloro-2,6-diethylaniline) (MCDEA).…”
Section: Introductionmentioning
confidence: 99%
“…Their often unique property profiles are extremely low volatility, good thermal stability, wide liquid temperature range, nonflammability, good dissolving ability, low viscosity, negligible vapor pressure, and high ionic conductivity. [21][22][23][24][25][26][27][28][29] The aim of this study is the use of natural amino acid building blocks for efficient synthesis of novel biodegradable and chiral nanostructured PAIs, using molten tetrabutylammonium bromide (TBAB) as green medium. PAIs with main-chain chirality were synthesized via direct step-growth polymerization reaction of different chiral diacids (4a-4d) with 4,4′-methylenebis(3-chloro-2,6-diethylaniline) (MCDEA).…”
Section: Introductionmentioning
confidence: 99%