1. N-Methylation of Self-Immolative Thiocarbamates Provides Insights into the Mechanism of Carbonyl Sulfide Release
- Author
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Christopher H. Hendon, Jenna L. Mancuso, Carolyn M Levinn, Michael D. Pluth, Haley M Smith, and Rachel E Lutz
- Subjects
010405 organic chemistry ,Hydrogen sulfide ,Organic Chemistry ,equipment and supplies ,010402 general chemistry ,01 natural sciences ,Combinatorial chemistry ,Article ,0104 chemical sciences ,Thiocarbamate ,chemistry.chemical_compound ,Deprotonation ,Aniline ,chemistry ,Isothiocyanate ,Reactivity (chemistry) ,Thiocarbamates ,Carbonyl sulfide - Abstract
Hydrogen sulfide (H(2)S) is an important biomolecule, and self-immolative thiocarbamates have shown great promise as triggerable H(2)S donors with suitable analogous control compounds, however thiocarbamates with electron-deficient payloads are less efficient H(2)S donors. We report here the synthesis and study of a series of N-methylated esterase-triggered thiocarbamates that block the postulated unproductive deprotonation-based pathway for these compounds. The relative reaction profiles for H(2)S release across a series of electron-rich and electron-poor N-Me aniline payloads are examined experimentally and computationally. We show that thiocarbamate N-methylation does block some side reactivity and increases the H(2)S release profiles for electron-poor donors. Additionally, we show that isothiocyanate release is not a competitive pathway, and rather that the reduced efficiency of electron-poor donors is likely due to other side reactions. more...
- Published
- 2021
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