Journal
JOURNAL OF ORGANIC CHEMISTRY
Volume 82, Issue 2, Pages 1248-1253Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.6b02531
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Funding
- Mizutani Foundation for Glycoscience
- Nagase Science Technology Foundation
- Protein Research Foundation
- [JP26282211]
- [JP26102732]
- [JP26882036]
- [JP16H01162]
- [JP16K16638]
- Grants-in-Aid for Scientific Research [16H01162, 15H05850, 26248031, 16K16638, 15K13699, 26282211] Funding Source: KAKEN
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A formal total synthesis of L-ossamine was achieved. The key feature of the synthesis was the decarboxylative functionalization of a threonine derivative using visible-light-mediated photoredox catalysis. This reaction was implemented in a flow reactor, allowing for the efficient conversion to the desired product.
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