File | |
language |
eng
|
Author |
Ohkado, Ryoma
Department of Chemistry, Interdisciplinary Graduate School of Science and Engineering, Shimane University, 1060 Nishikawatsu, Matsue 690-8504, Japan
Ishikawa, Tatsuro
Department of Chemistry, Interdisciplinary Graduate School of Science and Engineering, Shimane University, 1060 Nishikawatsu, Matsue 690-8504, Japan
|
Description | A unique coupled redox organocatalysis system using flavin and iodine catalysts efficiently promoted the metal-free aerobic oxidative direct sulfenylation of indoles with thiols at ambient temperature without any sacrificial reagents, except environmentally benign molecular oxygen. Biomimetic flavin catalysis plays multiple roles in aerobic oxidative transformations, not only regenerating I2 from in situ generated I−, but also converting thiols into disulfides.
|
Journal Title |
Green Chemistry
|
Volume | 20
|
Start Page | 984
|
End Page | 988
|
ISSN | 1463-9262
|
ISSN(Online) | 1463-9270
|
Published Date | 2018-2-5
|
DOI | |
Publisher | The Royal Society of Chemistry
|
NII Type |
Journal Article
|
Format |
PDF
|
Relation | |
Text Version |
著者版
|
Gyoseki ID | e33058
|
OAI-PMH Set |
Faculty of Science and Engineering
|
Remark | Green Chem., 2018,20, 984-988
|