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Alkoxyl- and carbon-centered radicals as primary agents for degrading non-phenolic lignin-substructure model compounds. Yasunori Ohashi, Yukiko Uno, Rudianto Amirta, Takahito Watanabe, Yoichi Honda, Takashi Watanabe
, Org. Biomol. Chem.
, 2011
, 9
, 2481
- 292. Purpurogallin. Part VI. Mechanism of the oxidation of pyrogallol. Alan Critchlow, Robert D. Haworth, Peter L. Pauson
, J. Chem. Soc.
, 1951
, 1318
- Selective photocatalytic C–C bond cleavage under ambient conditions with earth abundant vanadium complexes. Sarifuddin Gazi, Wilson Kwok Hung Ng, Rakesh Ganguly, Adhitya Mangala Putra Moeljadi, Hajime Hirao, Han Sen Soo
, Chem. Sci.
, 2015
, 6
, 7130
- Transition-metal catalyzed valorization of lignin: the key to a sustainable carbon-neutral future. Markus D. Kärkäs, Bryan S. Matsuura, Timothy M. Monos, Gabriel Magallanes, Corey R. J. Stephenson
, Org. Biomol. Chem.
, 2016
, 14
, 1853
- Studies related to the chemistry of melanins. Part IV. Oxidation of 5,6-dimethoxyindoline. S. N. Mishra, G. A. Swan
, J. Chem. Soc. C
, 1967
, 1428
- Structures of the red sandalwood pigments santalins A and B. Alberto Arnone, Lorenzo Camarda, Lucio Merlini, Gianluca Nasini
, J. Chem. Soc., Perkin Trans. 1
, 1975
, 186
- Transaminase-mediated synthesis of enantiopure drug-like 1-(3′,4′-disubstituted phenyl)propan-2-amines. Ágnes Lakó, Zsófia Molnár, Ricardo Mendonça, László Poppe
, RSC Adv.
, 2020
, 10
, 40894
- Electrochemical oxidation of aromatic ethers. Part 9. Proof of the mode of aryl–aryl coupling in 4-benzylisochroman-3-ones, and the oxidative reactions of 2-and 3-aralkyl-1,2,3,4-tetrahydroisoquinolines. Amera J. Majeed, Malcolm Sainsbury, Stephen A. Hall
, J. Chem. Soc., Perkin Trans. 1
, 1984
, 833
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Resorcin[4]arene-derived mono-, bis- and tetra-imidazolium salts as ligand precursors for Suzuki–Miyaura cross-coupling. Hani El Moll, David Sémeril, Dominique Matt, Loïc Toupet, Jean-Jacques Harrowfield
, Org. Biomol. Chem.
, 2012
, 10
, 372
- Heterogeneous catalytic oxidation for lignin valorization into valuable chemicals: what results? What limitations? What trends?. R. Behling, S. Valange, G. Chatel
, Green Chem.
, 2016
, 18
, 1839