41075-43-8Relevant academic research and scientific papers
Ruthenium(II)-Catalyzed Redox-Neutral Oxidative Cyclization of Benzimidates with Alkenes with Hydrogen Evolution
Manikandan, Rajendran,Tamizmani, Masilamani,Jeganmohan, Masilamani
, p. 6678 - 6681 (2017)
1H-Isoindoles and 2H-isoindoles are synthesized via a ruthenium-catalyzed oxidant-free cyclization of benzimidates with alkenes at room temperature with the liberation of H2. Later, 1H-isoindoles were converted into nitrogen-containing heterocy
Benzimidates as gem-Diamidation and Amidoindolyzation Cascade Synthons with a Hydrated NiII Catalyst
Nandi, Rajesh,Mandal, Prakash K.,Kayet, Anirban,Bhattachariya, Tamalika,Ghosh, Sukla,Maiti, Dilip K.
supporting information, p. 3474 - 3478 (2020/04/20)
We contributed a new benzimidate chemistry through moisture-insensitive NiII/NiII-FeIII combo-catalysis for a simultaneous 2-3 bond-forming gem-diamidation and amidoindolyzation cascade reaction to construct symmetrical an
2-OXAZOLINES FROM AMIDES VIA IMIDATES
Meyers, A. I.,Hanagan, Mary Ann,Mazzu, Arthur L.
, p. 361 - 367 (2007/10/02)
Chiral oxazolines useful in asymmetric synthesis of o-substituted phthalides and benzoic acids are readily prepared from the benzamides via their imino ethers.
