Total synthesis of optically active integerrimine, a twelve-membered dilactonic pyrrolizidine alkaloid of retronecine type. II. Enantioselective synthesis of (+)-retronecine
- 31 December 1986
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 27 (38) , 4605-4608
- https://doi.org/10.1016/s0040-4039(00)85016-9
Abstract
No abstract availableThis publication has 22 references indexed in Scilit:
- Synthetic studies on pyrrolizidine alkaloid antitumor agents. Enantioselective synthesis of retronecine and its enantiomer from D-glucoseThe Journal of Organic Chemistry, 1985
- Enantioselective synthesis of seven pyrrolizidine diols from a single precursorThe Journal of Organic Chemistry, 1985
- Nonstabilized imidate ylides by the desilylation method: a route to the pyrrolizidine alkaloids retronecine and indicineThe Journal of Organic Chemistry, 1985
- Novel synthesis of the pyrrolizidine skeleton by sulfenocycloamination. Total synthesis of (.+-.)-retronecine and (.+-.)-turneforcidineThe Journal of Organic Chemistry, 1983
- The Enantioselective Synthesis of (+)-Retronecine, (—)-Platynecine, and (+)-Croalbinecine and Its C-1 EpimerHETEROCYCLES, 1983
- A TOTAL SYNTHESIS OF (±)-INTEGERRIMINEChemistry Letters, 1982
- Stereoselective Total Synthesis of Necine Bases, (±)-Retronecine and (±)-TurneforcidineHETEROCYCLES, 1982
- A Synthesis of (+)-2-Oxa-6-azabicyclo[3.3.0]octan-3-one (The Geissman-Waiss Lactone): A Synthon for Some NecinesHETEROCYCLES, 1982
- The saturated pyrrolizidine diols. III. A partial synthesis of turneforcidineAustralian Journal of Chemistry, 1969
- 3. Alkaloids of senecio. Part I. RetrorsineJournal of the Chemical Society, 1935