Coupled Flavin-Iodine Redox Organocatalysts: Aerobic Oxidative Transformation from N-Tosylhydrazones to 1,2,3-Thiadiazoles

ACS Catalysis Volume 7 Issue 8 Page 4986-4989 published_at 2017-6-29
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Title
Coupled Flavin-Iodine Redox Organocatalysts: Aerobic Oxidative Transformation from N-Tosylhydrazones to 1,2,3-Thiadiazoles
Creator
Ishikawa Tatsuro
Kimura Maasa
Kumoi Takuma
Source Title
ACS Catalysis
Volume 7
Issue 8
Start Page 4986
End Page 4989
Journal Identifire
ISSN 2155-5435
Descriptions
A bioinspired two-component redox organocatalyst system using 1,10-bridged flavinium and NH4I was developed to perform environmentally friendly aerobic oxidative ring formation of 1,2,3-thiadiazoles from N-tosylhydrazones and sulfur. The redox organocatalysis of the flavinium promoted the iodine-catalyzed system without the use of any sacrificial reagents, except for environmentally benign molecular oxygen.
Subjects
redox organocatalyst
flavin
iodine
aerobic oxidation
thiadiazole
Language
eng
Resource Type journal article
Publisher
American Chemical Society
Date of Issued 2017-6-29
Rights
Copyright © 2017 American Chemical Society
Publish Type Accepted Manuscript
Access Rights open access
Relation
[DOI] 10.1021/acscatal.7b01535
[URI] https://pubs.acs.org/journal/accacs
Remark ACS Catal. 2017, 7, 8, 4986-4989 Publication Date:June 29, 2017