53924-28-0Relevant articles and documents
Halogen bonding organocatalysis enhanced through intramolecular hydrogen bonds
Berryman, Orion B.,Decato, Daniel A.,Riel, Asia Marie S.,Sun, Jiyu
supporting information, p. 1378 - 1381 (2022/02/09)
Recent results indicate a halogen bond donor is strengthened through direct interaction with a hydrogen bond to the electron-rich belt of the halogen. Here, this Hydrogen Bond enhanced Halogen Bond (HBeXB) plays a clear role in a catalyst. Our HBeXB catalyst improves product conversion in a halide abstraction reaction over a traditional halogen bonding derivative. This journal is
An efficient synthesis of medicinally important indole based triarylmethanes by using propylphosphonic anhydride (T3P)
Cheruku, Srinivas,Nagaraju, Chaithra,Shetty, Poornima,Hassan A, Swarup,Nagarakere C, Sandhya,Manikyanally N, Kumara,Kempegowda, Mantelingu
supporting information, p. 1486 - 1494 (2020/04/08)
We have developed an economical and efficient method for the synthesis of medicinally and synthetically important indole-based triarylmethanes by using indoles and benzhydrols in the presence of propylphosphonic anhydride (T3P). This methodolog
Fluorinated Alcohol-Promoted Reaction of Chlorohydrocarbons with Diverse Nucleophiles for the Synthesis of Triarylmethanes and Tetraarylmethanes
Yu, Liping,Li, Shuai-Shuai,Li, Weina,Yu, Shitao,Liu, Qing,Xiao, Jian
, p. 15277 - 15283 (2019/01/04)
This article reports an efficient synthesis of triarylmethanes and tetraarylmethanes from chlorohydrocarbons with miscellaneous nucleophiles in fluorinated alcohols, featuring metal-free, wide substrate scope, excellent functional group tolerance, and mild reaction conditions.
