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1.
Angew Chem Int Ed Engl ; 57(35): 11441-11444, 2018 Aug 27.
Article in English | MEDLINE | ID: mdl-29978948

ABSTRACT

A chiral variant of B(C6 F5 )3 with a 3,3'-disubstituted binaphthyl backbone is shown to catalyze Nazarov cyclizations with high levels of enantio- and diastereocontrol. The parent B(C6 F5 )3 also promotes these ring closures efficiently. This electrocyclization is another example of the still small family of C-C bond formations mediated by B(C6 F5 )3 as the catalyst.

2.
J Am Chem Soc ; 140(2): 534-537, 2018 01 17.
Article in English | MEDLINE | ID: mdl-29271649

ABSTRACT

The combination of attractive supramolecular interactions of a hydrophobic AuI-metallopeptide with the shielding effect of flexible oligoethylene glycol chains provides access to a stepwise self-assembly of a AuI-metalloamphiphile in water. Kinetic control of the supramolecular polymer morphology is achieved using a temperature-dependent assembly protocol, which yields low dispersity supramolecular polymers (metastable state I) or helical bundled nanorods (state II).


Subject(s)
Gold/chemistry , Metalloproteins/chemistry , Peptides/chemistry , Water/chemistry , Kinetics , Models, Molecular
3.
Chemistry ; 23(25): 6048-6055, 2017 May 02.
Article in English | MEDLINE | ID: mdl-28181714

ABSTRACT

The ligation of gold(I) metalloamphiphiles with biomolecules is reported, using water-soluble AuI -N-alkynyl substituted maleimide complexes. For this purpose, two different polar ligands were applied: 1) a neutral, dendritic tetraethylene glycol-functionalized phosphane and 2) a charged, sulfonated N-heterocyclic carbene (NHC). The retro Diels-Alder reaction of a furan-protected maleimide gold(I) complex, followed by cycloaddition with a diene-functionalized biotin under mild conditions leads to a novel gold(I) metalloamphiphile. The strong streptavidin-biotin binding affinity in buffered aqueous solution of the resulting biotin alkynyl gold(I) phosphane conjugate remains intact. The cytotoxicity of the biotinylated gold(I) complex against a T47D human breast cancer cell line is higher than for cisplatin.

4.
Chem Commun (Camb) ; 51(25): 5253-6, 2015 Mar 28.
Article in English | MEDLINE | ID: mdl-25001106

ABSTRACT

We report a short synthetic route for the preparation of a peptidic Au(I)-metalloamphiphile which, in buffered environments of physiological ionic strength, self-assembles into luminescent micellar nanostructures of 14 nm in diameter.


Subject(s)
Gold/chemistry , Luminescence , Micelles , Peptides/chemical synthesis , Surface-Active Agents/chemical synthesis , Water/chemistry , Molecular Structure , Particle Size , Peptides/chemistry , Surface Properties , Surface-Active Agents/chemistry
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