Strictosidine, the common precursor for monoterpenoid indole alkaloids with 3 α and 3 β configuration
- 31 December 1978
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 19 (18), 1593-1596
- https://doi.org/10.1016/s0040-4039(01)94613-1
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Biosynthesis of camptothecin. II. Confirmation that isovincoside, not vincoside, is the penultimate biosynthetic precursor of indole alkaloidsTetrahedron Letters, 1977
- Isovincoside (strictosidine), the key intermediate in the enzymatic formation of indole alkaloidsFEBS Letters, 1977
- Strictosidine (isovincoside): the key intermediate in the biosynthesis of monoterpenoid indole alkaloidsJournal of the Chemical Society, Chemical Communications, 1977
- ‘One-pot’ biomimetic synthesis of 19β-heteroyohimbine alkaloidsJournal of the Chemical Society, Chemical Communications, 1977
- Biosynthesis of camptothecin. I. Definition of the overall pathway assisted by carbon-13 nuclear magnetic resonance analysisJournal of the American Chemical Society, 1974
- Biomimetic inversion of C-3 in monoterpenoid indole alkaloidsJournal of the Chemical Society, Chemical Communications, 1974
- Further studies on rearrangements during biosynthesis of indole alkaloidsJournal of the Chemical Society D: Chemical Communications, 1971
- THE MITRAGYNA SPECIES OF ASIA – Part. VII. Indole Alkaloids from the leaves ofMitragyna speciosaKorth.1, 2Planta Medica, 1966
- Notes - 3-Dehydro Derivatives of Some Indole AlkaloidsThe Journal of Organic Chemistry, 1956
- Alkaloide aus den Blättern von Rauwolfia canescens L. 4. Mitteilung über Rauwolfia‐AlkaloideHelvetica Chimica Acta, 1955