An article Introducing the Dihydro-1,3-azaboroles: Convenient Entry by a Three-Component Reaction, Synthetic and Photophysical Application WOS:000618171900042 published article about RING-CLOSING METATHESIS; RAY CRYSTAL-STRUCTURE; 1,2-AZABOROLYL COMPLEXES; MULTICOMPONENT REACTIONS; AZABOROLYL COMPLEXES; SANDWICH COMPLEXES; B-N; BORON; LIGAND; POLYMERIZATION in [Li, Jun; Daniliuc, Constantin G.; Kartha, Kalathil K.; Fernandez, Gustavo; Kehr, Gerald; Erker, Gerhard] Westfalische Wilhelms Univ Munster, Organ Chem Inst, D-48149 Munster, Germany in 2021.0, Cited 68.0. The Name is Chalcone. Through research, I have a further understanding and discovery of 94-41-7. Application In Synthesis of Chalcone
The (Fmes)BH2 center dot SMe2 reagent (7) reacts sequentially with an acetylene and, e.g., xylylisonitrile in a convenient three-component reaction to give a series of unprecedented dihydro-1,3-azaborole derivatives 16. The tolane-derived example 16a was deprotonated and used as a ligand in organometallic chemistry. Compounds 16 served as the starting materials for the straightforward synthesis of various dihydro-1,3-azaborinine derivatives by treatment with an isonitrile. Several diaryldihydro-1,3 azaboroles showed interesting photophysical properties such as aggregation-induced emission and high fluorescence quantum yields.
Welcome to talk about 94-41-7, If you have any questions, you can contact Li, J; Daniliuc, CG; Kartha, KK; Fernandez, G; Kehr, G; Erker, G or send Email.. Application In Synthesis of Chalcone
Reference:
Thiazolidine – Wikipedia,
,Thiazolidine – ScienceDirect.com