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Palladium-catalysed ortho-arylation of carbamate-protected phenols. Robin B. Bedford, Ruth L. Webster, Charlotte J. Mitchell
, Org. Biomol. Chem.
, 2009
, 7
, 4853
- 66. The synthesis of αβ-batyl (glycerol 2-octadecyl ether) analogue of cephalin, and melting-point data for batyl, chimyl, β-batyl, and β-chimyl alcohol and their derivatives. T. H. Bevan, T. Malkin
, J. Chem. Soc.
, 1960
, 350
- Synthesis of novel homoazanucleosides and their peptidyl analogs. Rahul Vilas Salunke, Pawan Kumar Mishra, Yogesh S. Sanghvi, Namakkal G. Ramesh
, Org. Biomol. Chem.
, 2020
, 18
, 5639
- Hydrogen-bond basicity of secondary and tertiary amides, carbamates, ureas and lactams. Jean-Yves Le Questel, Christian Laurence, Abdeljalil Lachkar, Maryvonne Helbert, Michel Berthelot
, J. Chem. Soc., Perkin Trans. 2
, 1992
, 2091
- Advances in the use of CO2 as a renewable feedstock for the synthesis of polymers. Bruno Grignard, Sandro Gennen, Christine Jérôme, Arjan W. Kleij, Christophe Detrembleur
, Chem. Soc. Rev.
, 2019
, 48
, 4466
- Synthesis of substituted phenylcarbamates of N-cyclobutylformylated chitosan and their application as chiral selectors in enantioseparation. Juan Zhang, Xiao-Chen Wang, Wei Chen, Zheng-Wu Bai
, Analyst
, 2016
, 141
, 4470
- XXI.—The chlorination of iodophenols. Part III. The chlorination of o-iodophenol. Samuel Buchan, Hamilton McCombie
, J. Chem. Soc.
, 1931
, 137
- CXXVIII.—The absorption spectra of various substances containing two, three, and four benzene nuclei. John Edward Purvis
, J. Chem. Soc., Trans.
, 1914
, 105
, 1372
- Index of subjects, 1934
, J. Chem. Soc.
, 1934
, 2034
- Formula index
, J. Chem. Soc.
, 1934
, 2056