2005
DOI: 10.1039/b510910h
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Dual chirality control of palladium(ii) complexes bearing tropos biphenyl diamine ligands

Abstract: Axial and center chirality of Pd complexes with tropos biphenyl secondary diamine ligands is shown to be controlled by chiral amide (R)-DABNTf, which can efficiently discriminate between two enantiomeric Pd complexes.

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Cited by 13 publications
(7 citation statements)
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References 20 publications
(5 reference statements)
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“…Scheme 3 Conversion of disulfonyl chlorides 7 or 8 into the corresponding cyclic imides 9 or 10 To synthesize 7, we attempted the dixanthate pathway first. After successful reduction of 2,2¢-dinitrobiphenyl 16 and diazotization of the resulting 2,2¢-diaminobiphenyl, the Leuckart reaction of the corresponding tetrafluoro- borate unfortunately afforded only tar byproducts. It was therefore decided to synthesize a biphenyl derivative which bears two sulfur functionalities in 2-and 2¢-positions, using the Suzuki coupling reaction.…”
Section: Figurementioning
confidence: 99%
“…Scheme 3 Conversion of disulfonyl chlorides 7 or 8 into the corresponding cyclic imides 9 or 10 To synthesize 7, we attempted the dixanthate pathway first. After successful reduction of 2,2¢-dinitrobiphenyl 16 and diazotization of the resulting 2,2¢-diaminobiphenyl, the Leuckart reaction of the corresponding tetrafluoro- borate unfortunately afforded only tar byproducts. It was therefore decided to synthesize a biphenyl derivative which bears two sulfur functionalities in 2-and 2¢-positions, using the Suzuki coupling reaction.…”
Section: Figurementioning
confidence: 99%
“…Consequently, the design of new catalysts, based on dynamic chirality control (e.g., N-chirality control [6] or dual chirality control of axial and N-chirality [7]) by C. R. Chimie 13 (2010) In this account, the recent advances on chiral stereochemically dynamic 2,2'-biphosphole ligands for applications in asymmetric catalysis are reported.…”
Section: Introductionmentioning
confidence: 99%
“…Molecular view of R[Sp,Sp,Sc]-2a space group: P2 1 2 1 2 1 , Flack's parameter: 0.06(14) 7. p-donor substituents on the phosphorus of phospholes do not affect the activation barrier according to experimental measurements and calculations.…”
mentioning
confidence: 99%
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“…or dual chirality control of axial and N-chirality 8 ) by a chiral activator through complexation is an important field.…”
Section: Introductionmentioning
confidence: 99%