File | |
Title |
Coupled Flavin-Iodine Redox Organocatalysts: Aerobic Oxidative Transformation from N-Tosylhydrazones to 1,2,3-Thiadiazoles
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Creator |
Ishikawa Tatsuro
Kimura Maasa
Kumoi Takuma
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Source Title |
ACS Catalysis
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Volume | 7 |
Issue | 8 |
Start Page | 4986 |
End Page | 4989 |
Journal Identifire |
ISSN 2155-5435
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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.
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Subjects | |
Language |
eng
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Resource Type | journal article |
Publisher |
American Chemical Society
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Date of Issued | 2017-6-29 |
Rights |
Copyright © 2017 American Chemical Society
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Publish Type | Accepted Manuscript |
Access Rights | open access |
Relation |
[DOI] 10.1021/acscatal.7b01535
[URI] https://pubs.acs.org/journal/accacs
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Remark | ACS Catal. 2017, 7, 8, 4986-4989 Publication Date:June 29, 2017 |