Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Alexander J. Pallenberg"'
Publikováno v:
Organic Process Research & Development. 8:287-290
A process for the preparation of pyropheophorbide a and its derivatives, including 3-devinyl-3-(1'-hexyloxy)ethyl-pyropheophorbide-a, otherwise known as HPPH, is provided. The process involves treating chlorin e6, in the form of its trimethyl ester
Publikováno v:
Synthetic Communications. 27:2943-2951
The preparation of hydrophilic 2,9-dialkyl-1,10-phenanthrolines, including phenanthroline-5-sulfonic acids and phenanthrolines with side chain functionality is described. Nucleophilic aromatic substitution chemistry is used to obtain regiochemically
Publikováno v:
Inorganic Chemistry. 36:4007-4010
The X-ray structure of [Cu(dnpp)2]PF6, where dnpp denotes 2,9-dineopentyl-1,10-phenanthroline, reveals a flattened tetrahedral copper complex with a dihedral angle between the least-squares planes of the ligands of only 63.4(1)°. Steric interactions
Publikováno v:
Polyhedron. 16:2711-2719
Structural features and physical properties of dmphen (2,9-dimethyl-1,10-phenanthroline) complexes with d10 metals ZnII, Ni0 and AgI were determined. These, together with the more well-known CuI compounds, constitute a rare example of an Ni0, CuI, Zn
Publikováno v:
Inorganic Chemistry. 36:172-176
This investigation focuses on a series of pseudotetrahedral complexes of the form Cu(NN)2+, where NN denotes a 1,10-phenanthroline ligand with alkyl substituents in the 2 and 9 positions and the counterion is PF6-. In these copper(I) systems, steric
Publikováno v:
Inorganic Chemistry. 34:2833-2840
Autor:
Alexander J. Pallenberg
Publikováno v:
ChemInform. 24
An improved method for the deprotection of synthetic peptides by catalytic hydrogenation is described. The new method allows for precise control of counterion stoichiometry and affords the peptides in high purity and yield, while avoiding the problem
Publikováno v:
ChemInform. 28
The preparation of hydrophilic 2,9-dialkyl-1,10-phenanthrolines, including phenanthroline-5-sulfonic acids and phenanthrolines with side chain functionality is described. Nucleophilic aromatic substitution chemistry is used to obtain regiochemically
Autor:
Alexander J. Pallenberg
Publikováno v:
Tetrahedron Letters. 33:7693-7696
An improved method for the deprotection of synthetic peptides by catalytic hydrogenation is described. The new method allows for precise control of counterion stoichiometry and affords the peptides in high purity and yield, while avoiding the problem
Publikováno v:
ChemInform. 21