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Synthetic Route

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Articles

Peer-Reviewed Papers

Synthesis of a series of aromatic benziporphyrins and heteroanalogues via tripyrrane-like intermediates derived from resorcinol and 2-methylresorcinol.Timothy D Lash et al.The Journal of organic chemistry, 76(15), 6295-6308 (2011-06-23) 2-Alkenal-scavenging ability of m-diphenols.Francisco J Hidalgo et al.Food chemistry, 160, 118-126 (2014-05-07) Cross-elicitation responses to 2-methoxymethyl-p-phenylenediamine under hair dye use conditions in p-phenylenediamine-allergic individuals.B Blömeke et al.The British journal of dermatology, 172(4), 976-980 (2014-09-23) [Long-term preservation of DNA in aqueous solutions in the presence of the chemical analogues of microbial autoregulators].O K Davydova et al.Mikrobiologiia, 75(5), 662-669 (2006-11-10) [Influence of chemical analogues of microbial autoregulators on the sensitivity of DNA to UV radiation].O K Davydova et al.Mikrobiologiia, 75(5), 654-661 (2006-11-10) A subchronic, teratologic, and dominant lethal study of 2-methylresorcinol in rats. II. Teratologic and dominant lethal study.T A Re et al.Fundamental and applied toxicology : official journal of the Society of Toxicology, 7(2), 293-298 (1986-08-01) A novel Helicosporium isolate and its antimicrobial and cytotoxic pigment.Hye Jung Choi et al.Journal of microbiology and biotechnology, 22(9), 1214-1217 (2012-07-21) Preparation of tripyrrane analogues from resorcinol and 2-methylresorcinol for applications in the synthesis of new benziporphyrin systems.Kae Miyake et al.Chemical communications (Cambridge, England), (2)(2), 178-179 (2004-01-23) A subchronic, teratologic, and dominant lethal study of 2-methylresorcinol in rats. I. Subchronic toxicity.T A Re et al.Fundamental and applied toxicology : official journal of the Society of Toxicology, 7(2), 287-292 (1986-08-01) Expanding cavitand chemistry: the preparation and characterization of [n]cavitands with n>=4.C Naumann et al.Chemistry (Weinheim an der Bergstrasse, Germany), 7(8), 1637-1645 (2001-05-15) Synthesis, characterization, X-ray structure and biological activities of C-5-bromo-2-hydroxyphenylcalix[4]-2-methyl resorcinarene.Hamza M Abosadiya et al.Molecules (Basel, Switzerland), 18(11), 13369-13384 (2013-11-01)

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