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Polyoxalates from biorenewable diols via Oxalate Metathesis Polymerization. John J. Garcia, Stephen A. Miller , Polym. Chem. , 2014 , 5 , 955

Refining plant oils and sugars to platform chemicals, monomers, and polymers. Swechchha Pandey, Bhausaheb S. Rajput, Samir H. Chikkali , Green Chem. , 2021 , 23 , 4255

Development and evaluation of a novel fluorescent chiral derivatization reagent DBD-S-M-Pro: first observation of four chiral amino acids in human hair. Xin Wang, Xiaoqi Sun, Yueying Jin, Shengyu Cheng, Yu Han, Minghui Zhang, Lingli Zhang, Xi-Ling Li, Chun-Yan Xu, Jun Zhe Min , Anal. Methods , 2023 , 15 , 884

Synthesis, characterization, photoluminescent and thermal properties of zinc(ii) 4′-phenyl-terpyridine compounds. Zhen Ma, Wanbing Lu, Baohuan Liang, Armando J. L. Pombeiro , New J. Chem. , 2013 , 37 , 1529

^BR2BodPR2: highly fluorescent alternatives to PPh3 and PhPCy2. Laura H. Davies, Ross W. Harrington, William Clegg, Lee J. Higham , Dalton Trans. , 2014 , 43 , 13485

Boron difluorides with formazanate ligands: redox-switchable fluorescent dyes with large stokes shifts. M.-C. Chang, A. Chantzis, D. Jacquemin, E. Otten , Dalton Trans. , 2016 , 45 , 9477

NMR metabolomic and microarray-based transcriptomic data integration identifies unique molecular signatures of hypersensitivity pneumonitis. Sanjukta Dasgupta, Nilanjana Ghosh, Priyanka Choudhury, Mamata Joshi, Sushmita Roy Chowdhury, Parthasarathi Bhattacharyya, Koel Chaudhury , Mol. Omics , 2022 , 18 , 101

The interaction of aromatic compounds with poly(vinylpyrrolidone) in aqueous solution. Part 5.—Binding isotherms for phenols and O-substituted phenols. Philip Molyneux, Sudhe Vekavakayanondha , J. Chem. Soc., Faraday Trans. 1 , 1986 , 82 , 291

The interaction of aromatic compounds with poly(vinylpyrrolidone) in aqueous solution. Part 6.—Polymer precipitation and viscosity studies with phenols and O-substituted phenols. Philip Molyneux, Sudhe Vekavakayanondha , J. Chem. Soc., Faraday Trans. 1 , 1986 , 82 , 635

cis-Diprotected cyclams and cyclens: a new route to symmetrically or asymmetrically 1,4-disubstituted tetraazamacrocycles and to asymmetrically tetrasubstituted derivatives. Frédéric Bellouard, Françoise Chuburu, Nelly Kervarec, Loïc Toupet, Smaïl Triki, Yves Le Mest, Henri Handel , J. Chem. Soc., Perkin Trans. 1 , 1999 , 3499