Product Details of 100-51-6. In 2020.0 J ORG CHEM published article about ONE-POT SYNTHESIS; N BOND FORMATION; BORROWING HYDROGEN; ANTIMALARIAL ACTIVITY; POTENTIAL INHIBITORS; SECONDARY ALCOHOLS; BENZYL ALCOHOLS; ALKYLATION; DERIVATIVES; AMINES in [Chun, Simin; Ahn, Jiwon; Lee, Seok Beom; Hong, Suckchang] Seoul Natl Univ, Coll Pharm, Res Inst Pharmaceut Sci, Seoul 08826, South Korea; [Putta, Ramachandra Reddy] Seoul Natl Univ, Coll Pharm, BK 21 Plus Project, Seoul 08826, South Korea; [Oh, Dong-Chan] Seoul Natl Univ, Coll Pharm, Nat Prod Res Inst, Seoul 08826, South Korea in 2020.0, Cited 73.0. The Name is Benzyl Alcohol. Through research, I have a further understanding and discovery of 100-51-6.
Herein, we describe novel iron-catalyzed transfer hydrogenation between alcohols and 1-(2-nitrophenyl)pyrroles for the synthesis of pyrrolo[1,2-alpha]quinoxalines. The tricarbonyl (eta(4)-cyclopentadienone) iron complex catalyzed the oxidation of alcohols and the reduction of nitroarenes, and the corresponding aldehydes and aniline were generated in situ. The resulting Pictet-Spengler-type annulation/oxidation completed the quinoxaline structure formation. The protocol tolerated various kinds of functional groups and provided 29 samples of 4-substituted pyrrolo[1,2-alpha]quinoxalines. The developed method was also applied for the synthesis of additional polyheterocycles.
About Benzyl Alcohol, If you have any questions, you can contact Chun, SM; Ahn, J; Putta, RR; Lee, SB; Oh, DC; Hong, SC or concate me.. Product Details of 100-51-6
Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles