| Literature DB >> 27356038 |
Shin Kamijo1, Go Takao2, Kaori Kamijo2, Masaki Hirota2, Keisuke Tao2, Toshihiro Murafuji3.
Abstract
A photo-induced substitutive introduction of an aldoxime functional group to carbon chains was achieved using photo-excited 4-benzoylpyridine as a C(sp(3) )-H bond cleaving agent and arylsulfonyl oxime as an aldoxime precursor. The non-acidic C-H bonds in various substances, including cycloalkanes, ethers, azacycles, and cyclic sulfides, were chemoselectively converted at ambient temperature under neutral conditions. The present transformation is a formal formylation of non-acidic C(sp(3) )-H bonds in a single step.Entities:
Keywords: 4-benzoylpyridine; C−H functionalization; aldoximes; photoreactions; radicals
Year: 2016 PMID: 27356038 DOI: 10.1002/anie.201603810
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336