Pure Appl. Chem., 1992, Vol. 64, No. 8, pp. 1121-1124
http://dx.doi.org/10.1351/pac199264081121
Synthetic study on an antitumor antibiotic rhizoxin by using an enzymatic process on prochiral β-substituted glutarates
CrossRef Cited-by Linking
- Williams David R., Werner Kim M., Feng Bainian: Total synthesis of rhizoxin D. Tetrahetron Lett 1997, 38, 6825. <http://dx.doi.org/10.1016/S0040-4039(97)01605-5>
- Schelhaas Michael, Waldmann Herbert: Schutzgruppenstrategien in der organischen Synthese. Angew Chem 1996, 108, 2192. <http://dx.doi.org/10.1002/ange.19961081805>
- Keck Gary E, Savin Kenneth A, Weglarz Michael A, Cressman Erik N.K: Synthetic studies on the rhizoxins. II. An approach to the C10C26 subunit using “substrate directed” allylstannane additions to aldehydes. Tetrahetron Lett 1996, 37, 3291. <http://dx.doi.org/10.1016/0040-4039(96)00578-3>
- Schoffers Elke, Golebiowski Adam, Johnson Carl R.: Enantioselective synthesis through enzymatic asymmetrization. Tetrahedron 1996, 52, 3769. <http://dx.doi.org/10.1016/S0040-4020(95)01021-1>
- Lafontaine Jennifer A., Leahy James W.: Rhizoxin synthetic studies. 1. Synthesis of the right hand [C(1) to C(9)]portion via a “pinwheel” approach. Tetrahetron Lett 1995, 36, 6029. <http://dx.doi.org/10.1016/0040-4039(95)01193-L>