118757-13-4Relevant academic research and scientific papers
Discovery and synthesis of 2-amino-1-methyl-1H-imidazol-4(5H)-ones as GPCR ligands; an approach to develop breast cancer drugs via GPCR associated PAR1 and PI3Kinase inhibition mechanism
Ashok,Shivananda,Manikandan,Chandrasekaran
, p. 641 - 651 (2019/02/26)
Efforts were taken to synthesis and characterize 2-amino-1-methyl-1H-imidazole-4(5H)-one derivatives (4a-u) through a four-step reaction. The achieved compounds in remarkable yield have characterized through standard analytical techniques such as FTIR, LC
Diels-Alder reactions of 1,5-dihydropyrano[3,4-b]pyrrol-5(1H)-ones, pyrrole-2,3-quinodimethane analogues; a new synthesis of indoles
Mark Jackson,Moody, Christopher J.
, p. 7447 - 7466 (2007/10/02)
The pyrano[3,4-b]pyrrol-5-(1H)-ones 7 are stable cyclic analogues of pyrrole-2,3-quinodimethane, and undergo Diels-Alder reaction with a range of acetylenes (dimethyl acetylenedicarboxylate, ethyl propiolate, ethyl trimethylsilylpropynoate, benzyne and the acetylene equivalent, phenyl vinyl sulfoxide), to give, after loss of carbon dioxide, indoles. The Diels-Alder reaction can be extended to the intramolecular variant to give cycloalka-[e]- and [g]-indoles.
THE MANGANESE(III) ACETATE OXIDATION OF N-PROTECTED INDOLINES
Ketcha, Daniel M.
, p. 2151 - 2154 (2007/10/02)
A variety of N-protected indolines can be oxidized to the corresponding indoles using manganese(III) acetate in glacial acetic acid.
