Extracurricular laboratory: Synthetic route of 500-22-1

Welcome to talk about 500-22-1, If you have any questions, you can contact Iwanejko, J; Brol, A; Szyja, B; Daszkiewicz, M; Wojaczynska, E; Olszewski, TK or send Email.. Safety of 3-Pyridinecarboxaldehyde

In 2019.0 TETRAHEDRON published article about STEREOSELECTIVE-SYNTHESIS; BIOLOGICAL EVALUATION; SYNTHETIC METHODS; ACIDS; INHIBITORS; DISCOVERY; ANALOGS; HCV; 2-AZANORBORNANE; PHOSPHONATES in [Iwanejko, Jakub; Brol, Anna; Wojaczynska, Elzbieta; Olszewski, Tomasz K.] Wroclaw Univ Sci & Technol, Dept Organ Chem, Fac Chem, Wybrzeze Wyspianskiego 27, PL-50370 Wroclaw, Poland; [Szyja, Bartlomiej] Wroclaw Univ Sci & Technol, Div Fuels Chem & Technol, Fac Chem, Gdanska St 7-9, PL-50344 Wroclaw, Poland; [Daszkiewicz, Marek] Polish Acad Sci, Inst Low Temp & Struct Res, Okolna St 2, PL-50422 Wroclaw, Poland in 2019.0, Cited 47.0. The Name is 3-Pyridinecarboxaldehyde. Through research, I have a further understanding and discovery of 500-22-1. Safety of 3-Pyridinecarboxaldehyde

A series of new aminophosphonate and phosphonic acid derivatives of hexahydroquinoxalin-2(1H)-ones and tetrahydroquinoxalin-2(1H)-ones were synthesised via hydrophosphonylation of the corresponding bicyclic imines with various dialkyl or diaryl H-phosphonates, H-phosphinates or H-phosphine oxides as phosphorus nucleophiles. The utility of the obtained compounds was demonstrated by their application as a source of phosphonate carbanion in the Horner-Wadsworth-Emmons (HWE) reaction leading to new bicyclic amines with an exocyclic, and unexpectedly, also endocyclic double bond depending on the structure of the aldehyde used. (C) 2019 Elsevier Ltd. All rights reserved.

Welcome to talk about 500-22-1, If you have any questions, you can contact Iwanejko, J; Brol, A; Szyja, B; Daszkiewicz, M; Wojaczynska, E; Olszewski, TK or send Email.. Safety of 3-Pyridinecarboxaldehyde

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem