《Mechanistic pathways for halogen dance reactions in bromo-thiophenes: a cascade-like pattern》 was published in Journal of Chemical Sciences (Berlin, Germany) in 2020. These research results belong to Sakhaee, Nader; Sakhaee, Sahar; Mobaraki, Akbar; Takallou, Ahmad; Sakhaee, Mohammad Hossein. Recommanded Product: 3141-27-3 The article mentions the following:
Ever since the halogen dance reaction was discovered by Bunnet et al, synthetic chemists have utilized the transformation in many desirable ways to build substituted heterocyclic target mols. of all kind. Using DFT-Cam-B3LYP/ land2dz computations and focused on Hannes Frohlich et al. Halogen dance (HD) reactions of bromothiophenes, a new bromo-bridged transition state (TS) is proposed. This bromo-bridged TS was then used to put forth eight possible isomerization as well as eight possible disproportionation paths. These mechanistic pathways were then carefully inspected based on TS’s energy and protonation/deprotonation steps to find the most suitable pathways. Collectively these mechanistic pathways joined like a jigsaw puzzle to give, for the first-time, a fully comprehensive cascade-like pattern for base-catalyzed halogen dance in its entirety. The present work may well shed light on a dynamic domino mechanism which dominates the realm of nonaqueous strongly basic medium, organic chem., reactions. After reading the article, we found that the author used 2,5-Dibromothiophene(cas: 3141-27-3Recommanded Product: 3141-27-3)
2,5-Dibromothiophene(cas: 3141-27-3) , is mainly used as pharmaceutical intermediate and synthesis intermediate. 2,5-Dibromothiophene may be used in the preparation of soluble α,ω-diformyl-a-oligothiophenes.Recommanded Product: 3141-27-3
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary