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- Azafulvenium methides: new extended dipolar systems. Oliver B. Sutcliffe, Richard C. Storr, Thomas L. Gilchrist, Paul Rafferty
, J. Chem. Soc., Perkin Trans. 1
, 2001
, 1795
- Recent advancement in the synthesis of diverse spiro-indeno[1,2-b]quinoxalines: a review. Ruby Singh, Diksha Bhardwaj, Munna Ram Saini
, RSC Adv.
, 2021
, 11
, 4760
- X-ray crystal structures and anti-breast cancer property of 3-tert-butoxycarbonyl-2-arylthiazolidine-4-carboxylic acids. Rohidas M. Jagtap, Shridhar H. Thorat, Rajesh G. Gonnade, Ayesha A. Khan, Satish K. Pardeshi
, New J. Chem.
, 2018
, 42
, 1078
- Structural features and applications of metal–organic frameworks containing thiazole- and thiazolidine-based spacers. A. Rossin, G. Giambastiani
, CrystEngComm
, 2015
, 17
, 218
- Gastrointestinal tract mechanism of nitrite capture modeled on the self assembled monolayer of thioproline for electrochemical nitrite determination. Nimisha Singh, Khushbu Patel, Suban K. Sahoo, Ranjan K. Pati, Rajender Kumar
, J. Mater. Chem. A
, 2017
, 5
, 3389
- Sequential polypeptides. Part VI. The synthesis of some sequential polypeptide collagen models containing proline analogues. R. Fairweather, J. H. Jones
, J. Chem. Soc., Perkin Trans. 1
, 1972
, 2475
- Rearrangement of thiazolidine derivatives – a synthesis of a chiral fused oxathiane–γ-lactam bicyclic system. Karolina Kamińska, Dominika Iwan, Jakub Trojnar, Marek Daszkiewicz, Joanna E. Rode, Jacek Wojaczyński, Elżbieta Wojaczyńska
, Org. Biomol. Chem.
, 2023
, 21
, 9182
- Selenazolidine: a selenium containing proline surrogate in peptide science. E. Cordeau, S. Cantel, D. Gagne, A. Lebrun, J. Martinez, G. Subra, C. Enjalbal
, Org. Biomol. Chem.
, 2016
, 14
, 8101
- 4-Methylpseudoproline derived from α-methylserine – synthesis and conformational studies. Joanna Katarzyńska, Adam Mazur, Wojciech M. Wolf, Simon J. Teat, Stefan Jankowski, Mirosław T. Leplawy, Janusz Zabrocki
, Org. Biomol. Chem.
, 2012
, 10
, 6705
- A synthetic approach to ‘click’ neoglycoprotein analogues of EPO employing one-pot native chemical ligation and CuAAC chemistry. D. J. Lee, A. J. Cameron, T. H. Wright, P. W. R. Harris, M. A. Brimble
, Chem. Sci.
, 2019
, 10
, 815