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CYP199A4 catalyses the efficient demethylation and demethenylation of para -substituted benzoic acid derivatives . Tom Coleman, Rebecca R. Chao, John B. Bruning, James J. De Voss, Stephen G. Bell
, RSC Adv.
, 2015
, 5
, 52007
Synthesis of chiloglottones – semiochemicals from sexually deceptive orchids and their pollinators . Jacqueline Poldy, Rod Peakall, Russell Allan Barrow
, Org. Biomol. Chem.
, 2009
, 7
, 4296
First syntheses of the biologically active fungal metabolites pestalotiopsones A, B, C and F . Andrew Michael Beekman, Edwin Castillo Martinez, Russell Allan Barrow
, Org. Biomol. Chem.
, 2013
, 11
, 1109
Long-chain phenols. Part 16. A novel synthesis of homologous orsellinic acids and their methyl ethers . Aziz A. Durrani, John H. P. Tyman
, J. Chem. Soc., Perkin Trans. 1
, 1980
, 1658
Crucial gating residues govern the enhancement of peroxygenase activity in an engineered cytochrome P450 O -demethylase . Panxia Zhao, Yiping Jiang, Qian Wang, Jie Chen, Fuquan Yao, Zhiqi Cong
, Chem. Sci.
, 2024
, 15
, 8062
Phenyl-γ-valerolactones and phenylvaleric acids, the main colonic metabolites of flavan-3-ols: synthesis, analysis, bioavailability, and bioactivity . Pedro Mena, Letizia Bresciani, Nicoletta Brindani, Iziar A. Ludwig, Gema Pereira-Caro, Donato Angelino, Rafael Llorach, Luca Calani, Furio Brighenti, Michael N. Clifford, Chris I. R. Gill, Alan Crozier, Claudio Curti, Daniele Del Rio
, Nat. Prod. Rep.
, 2019
, 36
, 714
Total synthesis of moracin C . Graeme D. McAllister, Richard C. Hartley, Michael J. Dawson, Andrew R. Knaggs
, J. Chem. Soc., Perkin Trans. 1
, 1998
, 3453
The chemistry of fungi. Part LXXI. Synthesis of 3,5-dihydroxy-4-methylbenzoic acid . David R. Briggs, W. Basil Whalley
, J. Chem. Soc., Perkin Trans. 1
, 1976
, 1382
Synthesis of some precursors of 1,3,8-naphthalenetriol and related compounds . D. W. Cameron, E. M. Hildyard
, J. Chem. Soc. C
, 1968
, 166
The bromination of some derivatives of resorcinol . J. R. Cannon, T. M. Cresp, B. W. Metcalf, M. V. Sargent, G. Vinciguerra, J. A. Elix
, J. Chem. Soc. C
, 1971
, 3495