Muthukrishnan, I; Karuppasamy, M; Vachan, BS; Rajput, D; Subbiah, N; Maheswari, CU; Sridharan, V in [Muthukrishnan, Isravel; Karuppasamy, Muthu; Vachan, B. S.; Maheswari, C. Uma; Sridharan, Vellaisamy] SASTRA Deemed Univ, Sch Chem & Biotechnol, Dept Chem, Thanjavur 613401, Tamil Nadu, India; [Rajput, Diksha; Sridharan, Vellaisamy] Cent Univ Jammu, Dept Chem & Chem Sci, Jammu 181143, Jammu & Kashmir, India; [Subbiah, Nagarajan] Natl Inst Technol, Dept Chem, Warangal 506004, Telangana, India published Chemodivergent synthesis of functionalized methanodibenzo[b,f][1,5]diazocin-13-ylmethanones and tetrahydroquinolinesviasolvent-dependent AB(2)and A(2)B(2)multicomponent annulation reactions in 2020.0, Cited 66.0. Product Details of 100-19-6. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.
A solvent-dependent chemodivergent approach was established for the synthesis of 6,12-methanodibenzo[b,f][1,5]diazocin-13-ylmethanones and 2,3,4-trisubstituted 1,2,3,4-tetrahydroquinolines involving two distinct multicomponent processes under basic conditions. The AB(2)three-component and A(2)B(2)four-component reactions between 2-aminoarylaldehydes and aryl methyl ketones under basic conditions afforded 6,12-methanodibenzo[b,f][1,5]diazocin-13-ylmethanones (up to 95% yield) and trisubstituted tetrahydroquinolines (up to 84% yield), respectively, based on the nature of the solvent employed. The skeletal diversity and complexity were attained in these high atom- and step-economical processes by creating four new bonds in a single synthetic operation from readily available simple starting materials.
Product Details of 100-19-6. Welcome to talk about 100-19-6, If you have any questions, you can contact Muthukrishnan, I; Karuppasamy, M; Vachan, BS; Rajput, D; Subbiah, N; Maheswari, CU; Sridharan, V or send Email.
Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem