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- Spectroscopic analysis of the pyrimidine(6–4)pyrimidone photoproduct: insights into the (6–4) photolyase reaction. Junpei Yamamoto, Yoshiyuki Tanaka, Shigenori Iwai
, Org. Biomol. Chem.
, 2009
, 7
, 161
- Iodide-promoted transformations of imidazopyridines into sulfur-bridged imidazopyridines or 1,2,4-thiadiazoles. Shi-Tang Ma, Xiao-Xiao Zhu, Jing-Yu Xu, Ying Li, Xiao-Mei Zhang, Cheng-Tao Feng, Yizhe Yan
, Chem. Commun.
, 2021
, 57
, 5338
- Stimulated Raman scattering microscopy: an emerging tool for drug discovery. W. J. Tipping, M. Lee, A. Serrels, V. G. Brunton, A. N. Hulme
, Chem. Soc. Rev.
, 2016
, 45
, 2075
- 15N labeling and analysis of 13C–15N and 1H–15N couplings in studies of the structures and chemical transformations of nitrogen heterocycles. Sergey L. Deev, Igor A. Khalymbadzha, Tatyana S. Shestakova, Valery N. Charushin, Oleg N. Chupakhin
, RSC Adv.
, 2019
, 9
, 26856
- Access to a primary aminosporopollenin solid support from plant spores. Sylvain Barrier, Andreas Löbbert, Alia J. Boasman, Andrew N. Boa, Mark Lorch, Stephen L. Atkin, Grahame Mackenzie
, Green Chem.
, 2010
, 12
, 234
- Quantitative detection of isotopically enriched E. coli cells by SERS. Malama Chisanga, Howbeer Muhamadali, Richard Kimber, Royston Goodacre
, Faraday Discuss.
, 2017
, 205
, 331
- The origin of the band at around 730 cm−1 in the SERS spectra of bacteria: a stable isotope approach. Patrick Kubryk, Reinhard Niessner, Natalia P. Ivleva
, Analyst
, 2016
, 141
, 2874
-
7-Deazapurine
biosynthesis: NMR study of toyocamycin biosynthesis in Streptomyces rimosus using 2-13C-7-15N-adenine. Ugo Battaglia, Jed E. Long, Mark S. Searle, Christopher J. Moody
, Org. Biomol. Chem.
, 2011
, 9
, 2227
- Biological degradation of tryptophan. C. E. Dalgliesh
, Q. Rev. Chem. Soc.
, 1951
, 5
, 227
- Set-up and screening of a fragment library targeting the 14-3-3 protein interface. Dario Valenti, João Filipe Neves, François-Xavier Cantrelle, Stanimira Hristeva, Domenico Lentini Santo, Tomáš Obšil, Xavier Hanoulle, Laura M. Levy, Dimitrios Tzalis, Isabelle Landrieu, Christian Ottmann
, Med. Chem. Commun.
, 2019
, 10
, 1796