Pure Appl. Chem., 1985, Vol. 57, No. 3, pp. 453-470
http://dx.doi.org/10.1351/pac198557030453
Stereochemical aspects of the biosynthetic routes leading to the pyrrolizidine and the quinolizidine alkaloids
CrossRef Cited-by Linking
- Rouden Jacques, Lasne Marie-Claire, Blanchet Jérôme, Baudoux Jérôme: (−)-Cytisine and Derivatives: Synthesis, Reactivity, and Applications. Chem. Rev. 2014, 114, 712. <http://dx.doi.org/10.1021/cr400307e>
- Finefield Jennifer M., Sherman David H., Kreitman Martin, Williams Robert M.: Enantiomere Naturstoffe: Vorkommen und Biogenese. angew chemie 2012, 124, 4886. <http://dx.doi.org/10.1002/ange.201107204>
- Finefield Jennifer M., Sherman David H., Kreitman Martin, Williams Robert M.: Enantiomeric Natural Products: Occurrence and Biogenesis. Angew Chem Int E 2012, 51, 4802. <http://dx.doi.org/10.1002/anie.201107204>
- Ober Dietrich, Gibas Lutz, Witte Ludger, Hartmann Thomas: Evidence for general occurrence of homospermidine in plants and its supposed origin as by-product of deoxyhypusine synthase. Phytochemisry 2003, 62, 339. <http://dx.doi.org/10.1016/S0031-9422(02)00553-8>
- Graser Gerson, Witte Ludger, J. Robins David, Hartmann Thomas: Incorporation of chirally deuterated putrescines into pyrrolizidine alkaloids: A reinvestigation. Phytochemisry 1998, 47, 1017. <http://dx.doi.org/10.1016/S0031-9422(98)80064-2>
- Böttcher Frank, Adolph Ralf-Dieter, Hartmann Thomas: Homospermidine synthase, the first pathway-specific enzyme in pyrrolizidine alkaloid biosynthesis. Phytochemisry 1993, 32, 679. <http://dx.doi.org/10.1016/S0031-9422(00)95154-9>
- Kinghorn A.D., Tosun A., Tosun F., Tanker M., Özden T., Nasution M.P., Hussain R.A.: 10α-hydroxymethylsparteine, a new type of quinolizidine alkaloid from Genista sessilifolia. Tetrahetron Lett 1991, 32, 5915. <http://dx.doi.org/10.1016/S0040-4039(00)79425-1>
- Saito Kazuki, Yamazaki Mami, Takamatsu Satoshi, Kawaguchi Akihiko, Murakoshi Isamu: Greening induced production of (+)-lupanine in tissue culture of Thermopsis lupinoides. Phytochemisry 1989, 28, 2341. <http://dx.doi.org/10.1016/S0031-9422(00)97980-9>