L. King

发表

N-acylglycine amidation: implications for the biosynthesis of fatty acid primary amides.

J. Vederas, D. Boger, D. Merkler, 1999, Biochemistry.

The enzymatic formation of novel bile acid primary amides.

J. Vederas, S. Barnes, D. Merkler, 2000, Archives of biochemistry and biophysics.

A pathway for the biosynthesis of fatty acid amides.

J. Vederas, D. Merkler, B. J. Wilcox, 1999, Advances in experimental medicine and biology.

Main group and transition metal compounds with silanediolate [R2SiO2]2− and α,ω-siloxane diolate [O(R2SiO)n]2− ligands

L. King, A. Sullivan, 1999 .

The reduction of DPN+ and TPN+ with sodium borohydride.

S. Chaykin, L. King, J. G. Watson, 1966, Biochimica et biophysica acta.

High oxidation state chromium, molybdenum and tungsten imido metallasiloxanes

M. Motevalli, L. King, A. Sullivan, 1999 .

Tritium-labeled DPN+ and TPN+.

S. Chaykin, L. King, J. G. Watson, 1966, Biochimica et biophysica acta.

Substituted hippurates and hippurate analogs as substrates and inhibitors of peptidylglycine alpha-hydroxylating monooxygenase (PHM).

Edward W. Lowe, Neil R. McIntyre, R. Kendig, 2008, Bioorganic & medicinal chemistry.

High oxidation state imido metallasiloxanes: synthesis and structural characterisation of novel bis-imido chromium(VI) and molybdenum(VI) compounds

M. Motevalli, L. King, A. Sullivan, 2000 .