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Total synthesis of 2′-deoxy-2′-arafluoro-tubercidin, -toyocamycin, -sangivamycin and certain related nucleosides . Birendra K. Bhattacharya, T. Sudhakar Rao, Ganapathi R. Revankar
, J. Chem. Soc., Perkin Trans. 1
, 1995
, 1543
Total synthesis of 2′-deoxy-2′-arafluorotoyocamycin and related nucleosides . Birendra K. Bhattacharya, Ganapathi R. Revankar
, J. Chem. Soc., Chem. Commun.
, 1995
, 115
Pyrrolopyrimidine nucleosides. Part X. Synthesis of certain 4,5-disubstituted 7-(β-D -ribofuranosyl)pyrrolo[2,3-d ]pyrimidines related to toyocamycin and sangivamycin . Barbara C. Hinshaw, Olga Leonoudakis, Karl H. Schram, Leroy B. Townsend
, J. Chem. Soc., Perkin Trans. 1
, 1975
, 1248
7-Deazapurine
biosynthesis: NMR study of toyocamycin biosynthesis in Streptomyces rimosus using 2-13 C-7-15 N-adenine . Ugo Battaglia, Jed E. Long, Mark S. Searle, Christopher J. Moody
, Org. Biomol. Chem.
, 2011
, 9
, 2227
Insight into the broadened substrate scope of nitrile hydratase by static and dynamic structure analysis . Dong Ma, Zhongyi Cheng, Lukasz Peplowski, Laichuang Han, Yuanyuan Xia, Xiaodong Hou, Junling Guo, Dejing Yin, Yijian Rao, Zhemin Zhou
, Chem. Sci.
, 2022
, 13
, 8417
Nitrile biosynthesis in nature: how and why? . Mingyu Liu, Shengying Li
, Nat. Prod. Rep.
, 2024
, 41
, 649
A mild process of carbon–carbon bond formation in aqueous medium: synthesis of bis(pyrrolo[2,3-d ]pyrimidinyl)methanes, a novel class of compounds . Meenakshi Sharma, Pulak J. Bhuyan
, RSC Adv.
, 2014
, 4
, 15709
Chemoenzymatic one-pot reaction from carboxylic acid to nitrile via oxime . Melissa Horvat, Victoria Weilch, Robert Rädisch, Sebastian Hecko, Astrid Schiefer, Florian Rudroff, Birgit Wilding, Norbert Klempier, Miroslav Pátek, Ludmila Martínková, Margit Winkler
, Catal. Sci. Technol.
, 2022
, 12
, 62
Targeting secondary protein complexes in drug discovery: studying the druggability and chemical biology of the HSP70/BAG1 complex . Lindsay E. Evans, Keith Jones, Matthew D. Cheeseman
, Chem. Commun.
, 2017
, 53
, 5167
A simple and novel method for the direct conversion of carboxylic acids into thioamides . Babak Kaboudin, Vahid Yarahmadi, Jun-ya Kato, Tsutomu Yokomatsu
, RSC Adv.
, 2013
, 3
, 6435