Metabolism of the sesquiterpenoid phytoalexins capsidiol and rishitin to their 13-hydroxy derivatives by plant cells

作者: E.W.B. Ward , A. Stoessl , J.B. Stothers

DOI: 10.1016/0031-9422(77)80120-9

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参考文章(7)
Toshio Murashige, Folke Skoog, A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue Cultures Physiologia Plantarum. ,vol. 15, pp. 473- 497 ,(1962) , 10.1111/J.1399-3054.1962.TB08052.X
George I. Birnbaum, A. Stoessl, S. H. Grover, J. B. Stothers, The Complete Stereostructure of Capsidiol. X-Ray Analysis and 13C Nuclear Magnetic Resonance of Eremophilane Derivatives Having trans-Vicinal Methyl Groups Canadian Journal of Chemistry. ,vol. 52, pp. 993- 1005 ,(1974) , 10.1139/V74-159
M. Gordon, A. Stoessl, J. B. Stothers, Post-infectional Inhibitors from Plants. IV.The Structure of Capsidiol, an Antifungal Sesquiterpene from Sweet Peppers Canadian Journal of Chemistry. ,vol. 51, pp. 748- 752 ,(1973) , 10.1139/V73-112
Robert C. Anderson, Donald M. Gunn, Judith Murray-Rust, Peter Murray-Rust, James S. Roberts, Vetispirane sesquiterpene glucosides from flue-cured virginia tobacco: structure, absolute stereochemistry, and synthesis. X-Ray structure of the p-bromobenzenesulphonate of one of the derived aglycones Journal of the Chemical Society, Chemical Communications. pp. 27- 28 ,(1977) , 10.1039/C39770000027