Sodium borohydride efficiently removes copper from amino acid-copper complexes

Tetrahedron Letters

Volumn 45, Issue 50, 2004, Pages 9297-9298

  Sailaja, Gummadi ^a   Nowshuddin, Shaik ^a   Rao, M N A ^a  

^a Divis Laboratories Limited   (India)

Author keywords

Copper removal; Copper amino acid complex; Sodium borohydride

Indexed keywords

AMINO ACID; COPPER COMPLEX; SODIUM BOROHYDRIDE;

ACYLATION; ANALYTIC METHOD; ARTICLE; CHEMICAL REACTION KINETICS; COMPLEX FORMATION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; PROTON NUCLEAR MAGNETIC RESONANCE;

EID: 8544256289     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.10.060     Document Type: Article

References (17)

1. A. Neuberger, and F. Sanger Biochem. J. 37 1943 515 518
2. R. Roeske, F.H.C. Stewart, R.J. Stedman, and V. duVigneaud J. Am. Chem. Soc. 78 1956 5883 5887
3. M. Zaoral Collect. Czech. Chem. Commun. 30 1965 1853 1868
4. U.F. Taylor, D.F. Dyckes, and J.R. Cox Jr Int. J. Pept. Protein Res. 19 1982 158 161
5. J.W. Scott, D. Parker, and D.R. Parrish Synth. Commun. 11 1981 303 314
6. R.L.M. Synge Biochem. J. 42 1948 99 104
7. S. Wiejak, E. Masiukiewicz, and B. Rzeszotarska Chem. Pharm. Bull. 49 2001 1189 1191
8. E. Wunsch, G. Fries, and A. Zwick Chem. Ber. 91 1958 542 547
9. R. Ledger, and F.H.C. Stewart Aust. J. Chem. 18 1965 1477 1484
10. R.L. Prestidge, D.R.K. Harding, J.E. Battersby, and W.S. Hancock J. Org. Chem. 40 1975 3287 3288
11. S. Kuwta, and H. Watanabe Bull. Chem. Soc. Jpn. 38 1965 676 677
12. H. Zahn, H. Zuber, W. Ditscher, D. Wegerle, and J. Meienhofer Chem. Ber. 89 1956 407 414
13. M.J. Bunegar, U.C. Dyer, A.P. Green, G.G. Gott, C.M. Jaggs, C.J. Lock, B.J.V. Mead, W.R. Spearing, P.D. Tiffin, N. Tremayne, and M. Woods Org. Process Res. Dev. 2 1998 334 336
14. Merck Index, 12th ed.; Merck&Co. Inc., 1996, p 1590
15. B.F. Erlanger, H. Sachs, and E. Brand J. Am. Chem. Soc. 76 1954 1806 1810
16. L. Younghee, and B.S. Richard Synthesis 1999 1495 1499
17. Chiral HPLC assays were carried out using a Chiralcel OD-R column, 4.6 x 250 mm, phosphate buffer(pH 2):acetonitrile (85:15) mobile phase; 0.75 mL/min at 35°C, 210 or 230 nm