Dissemin is shutting down on January 1st, 2025

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American Chemical Society, Organic Letters, 24(6), p. 4471-4474, 2004

DOI: 10.1021/ol048156h

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Site-Selective DNA Photocleavage Involving Unusual Photoinitiated Tautomerization of Chiral Tridentate Vanadyl(V) Complexes Derived fromN-Salicylidene α-Amino Acids

This paper is available in a repository.
This paper is available in a repository.

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Abstract

The titled vanadyl(V) complexes serve as efficient reagents for cleaving supercoiled plasmid DNA by photoinitiation. Complex 3d, derived from 2-hydroxy-1-naphthaldehyde and l-phenylalanine, exhibits a unique wedge feature, inducing a site-selective photocleavage at the C22-T23 of the bulge backbone for a HIV-27 DNA system at 0.1-5 muM. Transient absorption experiments for 3d indicate the involvement of LMCT with concomitant tautomerization, leading to an o-quinone-methide V-bound hydroxyl species responsible for the cleavage profiles. [structure: see text]