Novel pyrroles from sulfite-inhibited Maillard reactions: insight into the mechanism of inhibition
- 1 May 1988
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 53 (10), 2346-2349
- https://doi.org/10.1021/jo00245a039
Abstract
No abstract availableThis publication has 2 references indexed in Scilit:
- Vinylogous carbinolamine tumor inhibitors. 20. Comparison of the chemical reactivities and antineoplastic activities of .alpha.,.beta.-, .alpha.,.beta.'-, .beta.,.beta.'- and .alpha.,.alpha.'-bis[[[(2-propylamino)carbonyl]oxy]methyl] substituted pyrrolesJournal of Medicinal Chemistry, 1986
- Vinylogous carbinolamine tumor inhibitors. 19. Synthesis and antineoplastic activity of bis[[[(alkylamino)carbonyl]oxy]methyl]-substituted 3-pyrrolines as prodrugs of tumor inhibitory pyrrolebis(carbamates)Journal of Medicinal Chemistry, 1986