Formation of thioesters by dehydrogenative coupling of thiols and alcohols with H2 evolution
Author:
Publisher
Springer Science and Business Media LLC
Subject
Process Chemistry and Technology,Biochemistry,Bioengineering,Catalysis
Link
https://www.nature.com/articles/s41929-020-00514-9.pdf
Reference31 articles.
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2. Timothy Bannin, J. & Kiesewetter, M. K. Poly(thioester) by organocatalytic ring-opening polymerization. Macromolecules 48, 5481–5486 (2015).
3. Fukuyama, T., Lin, S.-C. & Li, L. Facile reduction of ethyl thiol esters to aldehydes: application to a total synthesis of (+)-neothramycin A methyl ether. J. Am. Chem. Soc. 112, 7050–7051 (1990).
4. Chandru, K., Gilbert, A., Butch, C., Aono, M. & Cleaves, H. J. The abiotic chemistry of thiolated acetate derivatives and the origin of life. Sci. Rep. 6, 29883 (2016).
5. Martina, N., Neelzb, V. & Spinnler, H.-E. Suprathreshold intensity and odour quality of sulphides and thioesters. Food Qual. Prefer. 15, 247–257 (2004).
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