Chen, Xia; Lu, Yuling; Guan, Zhenhua; Gu, Lianghu; Chen, Chunmei; Zhu, Hucheng; Luo, Zengwei; Zhang, Yonghui published the artcile< Synthesis of Succinimides via Intramolecular Alder-Ene Reaction of 1,6-Enynes>, Reference of 3240-10-6, the main research area is enyne diastereoselective Alder ene metal free green; succinimide stereoselective preparation.
A novel and convenient method has been developed for the facile synthesis of functionalized succinimide derivatives via intramol. Alder-ene reaction of 1,6-enynes. This reaction features mild and metal-free reaction conditions, which offers a green and efficient entry to synthetically important succinimide scaffolds. Preliminary mechanistic studies suggest that a diradical intermediate might be involved in this transformation.
Organic Letters published new progress about Alkenynes Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation). 3240-10-6 belongs to class chlorides-buliding-blocks, and the molecular formula is C9H5ClO2, Reference of 3240-10-6.
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics