Výsledky vyhledávání - "Bathini, Yadagiri"

Molecular Recognition and Binding of a GC Site-Avoiding Thiazole-Lexitropsin to the Decadeoxyribonucleotide d-[CGCAATTGCG]2:1H-NMR Evidence for Thiazole Intercalation

Autor: Surat Kumar, Sapse Am, Jaseja M, Richard T. Pon, Bathini Yadagiri, Zimmermann J, J. W. Lown

Publikováno v: Journal of Biomolecular Structure and Dynamics. 8:99-121

The structural and dynamic aspects of the interaction of the thiazole containing lexitropsin (1) with an oligodeoxyribonucleotide were studied by high field 1H-NMR spectroscopy. Complete assignment of the 1H-NMR resonances of lexitropsin 1 was accomp

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ed1dd47e19f377ec0b6d99b9865fc11
https://doi.org/10.1080/07391102.1990.10507792

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Convenient Routes to Substituted Benzimidazoles and Imidazolo[4,5-b]pyridines Using Nitrobenzene as Oxidant

Autor: Bathini Yadagiri, J. William Lown

Publikováno v: Synthetic Communications. 20:955-963

Various substituted benzimidazoles and imidazolo[4,5-b] pyridines 5a-c have been prepared by condensation of appropriate diamines and aldehydes in nitrobenzene. This method has been utilized to synthesize compounds 5f-h, which are analogues of the DN

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6109dafc43745748433aa3388c211059
https://doi.org/10.1080/00397919008052798

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Selective Cleavage of Benzoxazoles to o-Hydroxy-N-Substituted Anilines with Sodium Borohydride-Acetic Acid

Autor: Bathini Yadagiri, J. William Lown

Publikováno v: Synthetic Communications. 20:175-181

The utility of sodium borohydride in the presence of acetic acid in efficiently and selectively cleaving substituted benzoxazoles to o-hydroxy-N-substituted anilines in the presence of other functional groups is described. These conditions offer prac

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8aace5d6ddbe799b8508c63538ee0a16
https://doi.org/10.1080/00397919008052281

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Sequence specific molecular recognition and binding by a GC recognizing Hoechst 33258 analogue to the decadeoxyribonucleotide d-[CATGGCCATG]2: structural and dynamic aspects deduced from high field 1H-NMR studies

Autor: Jurg Zimmermann, J. William Lown, Richard T. Pon, Bathini Yadagiri, Surat Kumar

Publikováno v: Journal of biomolecular structuredynamics. 8(2)

The non-exchangeable and imino proton NMR resonances have been assigned of the 1:1 complex of an analogue 2 of Hoechst 33258 1 bound to the decadeoxyribonuycleotide d-[CATGGCCATG]2 by a combination of NOE difference, COSY and NOESYPH techniques. In c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8541da59f0ae9fe89352caed7e5ddfbb
https://pubmed.ncbi.nlm.nih.gov/1702637

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