60483-07-0Relevant articles and documents
Metal-free C(sp3)–H oxidation of 2-methylquinolines with PIDA under microwave irradiation
Jiang, Long,Huang, Yingyi,Yan, Yiyan,Xie, Yuanyuan
supporting information, p. 4149 - 4151 (2016/08/24)
An efficient metal-free protocol has been developed for the sp3C–H bond oxidation of 2-methylquinolines in the presence of PIDA under microwave irradiation, providing 2-quinolinecarboxaldehydes with moderate to high yields and excellent selectivities. A wide range of 2-quinolinecarboxaldehydes with different functional groups have been synthesized. A tentative mechanism has been presented to explain this highly selective oxidation process.
Oxidation of substituted pyridines PyrCHRSiMe3 (R=H, Me, Ph) and substituted quinolines QnCH2SiMe3 with hypervalent iodine reagents
Andrews, Ian P.,Lewis, Norman J.,McKillop, Alexander,Wells, Andrew S.
, p. 1151 - 1158 (2007/10/03)
Oxidation of a variety of substituted pyridines, PyrCHRSiMe3 (R = H, Me, Ph) and quinolines, QnCH2SiMe3 with hypervalent iodine reagents PIDA, (PhI(OCOCH3)2) and PIFA, (PhI(OCOCF3)2) has been studied. Oxy-desilylation with PIDA/TBAF gives low to moderate yields of PyrCHROR1 and QnCH2OR1 (R1 = H, Ac), while good yields of PyrCHROH and QnCH2OH are obtained when PIFA is used.