Chemical Communications 2003-08-07

A long-range chiral relay via tertiary amide group in asymmetric catalysis: new amino acid-derived N,P-ligands for copper-catalysed conjugate addition.

Andrei V Malkov, John B Hand, Pavel Kocovský

Index: Chem. Commun. (Camb.) (15) , 1948-9, (2003)

Full Text: HTML

Abstract

New N,P-ligands 4-6, derived from valinol and prolinol, respectively, have been developed for the asymmetric, copper(I)-catalysed conjugate addition of diethylzinc to unsaturated ketones; the tertiary amide group has been shown to effectively relay the chiral information from the ligand backbone to the active centre.


Related Compounds

  • 2-Amino-3-methylbu...

Related Articles:

Chiral bis(amino alcohol)oxalamide gelators-gelation properties and supramolecular organization: racemate versus pure enantiomer gelation.

2003-11-21

[Chemistry 9(22) , 5567-80, (2003)]

Synthesis of highly enantioenriched chiral alpha-aminoorganotins via diastereoselective ring opening of chiral N-(arenesulfonyl) 2-tributylstannyloxazolidines.

2009-08-21

[J. Org. Chem. 74(16) , 5822-38, (2009)]

General synthesis route to benanomicin-pradimicin antibiotics.

2007-01-01

[Chemistry 13(35) , 9791-823, (2007)]

Asymmetric synthesis of 8-aminoindolizidine from chiral 2-pyrroleimines.

2008-11-07

[J. Org. Chem. 73(21) , 8376-81, (2008)]

Order of binding of substrate to valyl-tRNA synthetase from Bacillus stearothermophilus in amino acid activation reaction.

1987-04-01

[Biochem. Int. 14(4) , 597-603, (1987)]

More Articles...