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Pure Appl. Chem., 1973, Vol. 34, No. 3-4, pp. 515-528

http://dx.doi.org/10.1351/pac197334030515

Comparative biosynthesis of fungal and plant phenalenones

R. Thomas

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  • Sigalov Mark, Shainyan Bagrat, Krief Pnina, Ushakov Igor, Chipanina Nina, Oznobikhina Larisa: Intramolecular interactions in dimedone and phenalen-1,3-dione adducts of 2(4)-pyridinecarboxaldehyde: Enol–enol and ring-chain tautomerism, strong hydrogen bonding, zwitterions. J Mole Struct 2011, 1006, 234. <http://dx.doi.org/10.1016/j.molstruc.2011.09.014>
  • Munde Tobias, Maddula Ravi K., Svatoš Aleš, Schneider Bernd: The biosynthetic origin of oxygen functions in phenylphenalenones of Anigozanthos preissii inferred from NMR- and HRMS-based isotopologue analysis. Phytochemisry 2011, 72, 49. <http://dx.doi.org/10.1016/j.phytochem.2010.10.007>
  • Otálvaro Felipe, Jitsaeng Kusuma, Munde Tobias, Echeverri Fernando, Quiñones Winston, Schneider Bernd: O-Methylation of phenylphenalenone phytoalexins in Musa acuminata and Wachendorfia thyrsiflora. Phytochemisry 2010, 71, 206. <http://dx.doi.org/10.1016/j.phytochem.2009.10.019>
  • Teimouri Mohammad B., Bazhrang Reihaneh: The synthesis of functionalized pyranophenalenones. Monatshefte für Chemie 2009, 140, 513. <http://dx.doi.org/10.1007/s00706-008-0082-6>
  • Luis Javier G., Fletcher Winston Q., Echeverri Fernando, Grillo Teresa A., Perales Aurea, González JoséA.: Intermediates with biosynthetic implications in de novo production of phenyl-phenalenone-type phytoalexins by Musa acuminata revised structure of emenolone. Tetrahedron 1995, 51, 4117. <http://dx.doi.org/10.1016/0040-4020(95)00129-V>
  • Hölscher Dirk, Schneider Bernd: The Biosynthetic Origin of the Central One-Carbon Unit of Phenylphenalenones in Anigozanthos preissii. Nat Prod Lett 1995, 7, 177. <http://dx.doi.org/10.1080/10575639508043208>
  • Chexal Kuldip K., Tamm Christoph, Hirotsu Ken, Clardy Jon: Gilmaniellin and Dechlorogilmaniellin, Two Novel Dimeric Oxaphenalenones. HCA 1979, 62, 1785. <http://dx.doi.org/10.1002/hlca.19790620611>
  • Ammon Herman L., Mazzocchi Paul H., Colicelli Elena J.: An investigation of the utility of using n.m.r. lanthanide shift reagents for13C assignments in selected aromatic ethers and ketones. A detailed description of the lanthanide induced shift ratio method for lanthanide shift reagent-substrate geometry analysis. Org Magn Reson 1978, 11, 1. <http://dx.doi.org/10.1002/mrc.1270110102>
  • Fujita Kazuyoshi, Suhara Masahiko, Sad�� Akira, Rohde Ottmar, Hayes Griffith O, Highet R.J, Edwards J.M: The calculation of the temperature dependence of NQR frequencies in chlorine and ��-nitrogen crystals. Journal of Magnetic Resonance (1969) 1975, 17, 314. <http://dx.doi.org/10.1016/0022-2364(75)90198-5>