Affiliation:
1. Institut de Chimie des Substances Naturelles CNRS UPR 2301 Université Paris-Sud Gif-sur-Yvette Cedex 91198 France
2. PPSM ENS Cachan CNRS Université Paris-Saclay Cachan 94235 France
Abstract
AbstractA new organocatalytic and environmentally friendly aerobic oxidative‐catalyzed nitroso‐Diels‐Alder (NDA) reaction of N‐arylhydroxylamines with dienecarbamates has been developed. 3,6‐Bis(2,2,2‐trifluoroethoxy)‐s‐tetrazine was found to be an effective catalyst to selectively oxidize various N‐arylhydroxylamines in the presence of molecular oxygen, but in the absence of photostimulation, as a terminal oxidant. In addition, active catalytic species can be generated in situ from commercially available 3,6‐dichlorotetrazine.
Funder
Institut Universitaire de France
Cited by
9 articles.
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