72450-41-0Relevant articles and documents
Enzymatic Synthesis of Methylated Terpene Analogues Using the Plasticity of Bacterial Terpene Synthases
Dickschat, Jeroen S.,Hou, Anwei,Lauterbach, Lukas
supporting information, (2020/02/11)
Methylated analogues of isopentenyl diphosphate were synthesised and enzymatically incorporated into methylated terpenes. A detailed stereochemical analysis of the obtained products is presented. The methylated terpene precursors were also used in conjunction with various isotopic labellings to gain insights into the mechanisms of their enzymatic formation.
Biosynthesis of the indolizidine alkaloid cyclizidine: incorporation of singly and doubly labelled precursors
Leeper, Finian J.,Shaw, Susan E.,Satish, Padma
, p. 131 - 141 (2007/10/02)
Incorporation of CH313C18O2Na and CD3CH213CO2Na into the indolizidine alkaloid cyclizidine 1, produced by Streptomyces species NCIB 11649, shows that the oxygen attached to C-2 is derived intact from acetate and that the cyclopropyl ring is derived from a single intact propionate unit.However, the level and stereochemistry of the incorporation of deuteriated sodium propionate indicates that it undergoes unexpected modification during incorporation into the cyclopropyl ring.