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- Dearomatisation approaches to spirocyclic dienones via the electrophilic activation of alkynes. Aimee K. Clarke, John T. R. Liddon, James D. Cuthbertson, Richard J. K. Taylor, William P. Unsworth
, Org. Biomol. Chem.
, 2017
, 15
, 233
- Silyl-naphthalene endoperoxides as switchable sources of singlet oxygen for bactericidal activity. Min Qu, Nan Wu, Wanqing Jiang, Lei Wang, Mahinur S. Akkaya, Engin U. Akkaya
, RSC Adv.
, 2021
, 11
, 19083
- Synthesis of diverse acyclic precursors to pyrroles for studies of prebiotic routes to tetrapyrrole macrocycles. Vanampally Chandrashaker, Marcin Ptaszek, Masahiko Taniguchi, Jonathan S. Lindsey
, New J. Chem.
, 2016
, 40
, 8786
- Synthesis and characterization of benzo- and naphtho[2,1-b:3,4-b′]dithiophene-containing oligomers for photovoltaic applications. Mirjam Löbert, Amaresh Mishra, Christian Uhrich, Martin Pfeiffer, Peter Bäuerle
, J. Mater. Chem. C
, 2014
, 2
, 4879
- A convergent approach to the marine natural product eleutherobin: synthesis of key intermediates and attempts to produce the basic skeleton. Gaia Scalabrino, Xiao-Wen Sun, John Mann, Anne Baron
, Org. Biomol. Chem.
, 2003
, 1
, 318
- Isoxazole mediated synthesis of 4-(1H)pyridones: improved preparation of antimalarial candidate GSK932121. Jorge Fernández, Jesús Chicharro, José M. Bueno, Milagros Lorenzo
, Chem. Commun.
, 2016
, 52
, 10190
- A highly enantioselective total synthesis of (+)-goniodiol. Edward W. Tate, Darren J. Dixon, Steven V. Ley
, Org. Biomol. Chem.
, 2006
, 4
, 1698
- A divergent and metal free synthesis of sulfoximine tethered imidazoles, imidazopyridines, imidazothiazoles, imidazobenzothiazines, thiazoles and selenazoles. S. R. K. Battula, V. P. Rama Kishore Putta, G. V. Subbareddy, I. E. Chakravarthy, V. Saravanan
, Org. Biomol. Chem.
, 2017
, 15
, 3742
- Review on fluorinated nucleoside/non-nucleoside FDA-approved antiviral drugs. Magda M. F. Ismail, Mohammed Salah Ayoup
, RSC Adv.
, 2022
, 12
, 31032
- Total synthesis and functional analysis of microbial signalling molecules. D. Leichnitz, L. Raguž, C. Beemelmanns
, Chem. Soc. Rev.
, 2017
, 46
, 6330