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Triplet Acetylenes as Synthetic Equivalents of 1,2-Bicarbenes, Part II: New Supramolecular Scaffolds from Photochemical Cycloaddition of Diarylacetylenes to 1,4-Cyclohexadienes.
- Published in:
- Chemistry - A European Journal, 2005, v. 11, n. 17, p. 4953, doi. 10.1002/chem.200500180
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Protected 32P-Labels in Deoxyribonucleotides: Investigation of Sequence Selectivity of DNA Photocleavage by Enediyne–, Fulvene–, and Acetylene–Lysine ConjugatesI.A. is grateful to the National Science Foundation (grant no.: CHE-0316598) for partial support of this research and to the 3M Company for an Untenured Faculty Award. N.L.G. thanks the National Science Foundation (grant no.: MCB 0316494) and the National Institutes of Health (grant no.: RO1 GM54008) for their support. We are also grateful for technical support from Dr. L. Keller (Florida State University Biology Department).
- Published in:
- Angewandte Chemie, 2006, v. 118, n. 22, p. 3748, doi. 10.1002/ange.200504479
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- Article
Protected 32P-Labels in Deoxyribonucleotides: Investigation of Sequence Selectivity of DNA Photocleavage by Enediyne–, Fulvene–, and Acetylene–Lysine ConjugatesI.A. is grateful to the National Science Foundation (grant no.: CHE-0316598) for partial support of this research and to the 3M Company for an Untenured Faculty Award. N.L.G. thanks the National Science Foundation (grant no.: MCB 0316494) and the National Institutes of Health (grant no.: RO1 GM54008) for their support. We are also grateful for technical support from Dr. L. Keller (Florida State University Biology Department).
- Published in:
- Angewandte Chemie International Edition, 2006, v. 45, n. 22, p. 3666, doi. 10.1002/anie.200504479
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- Article