Extended knowledge of 32717-95-6

Although many compounds look similar to this compound(32717-95-6)Synthetic Route of C16H16Cl2Cu2, numerous studies have shown that this compound(SMILES:C12=C(CCC3=C4CC2)[Cu+]1534[Cl-][Cu+]678(C9=C6CCC7=C8CC9)[Cl-]5), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

Synthetic Route of C16H16Cl2Cu2. So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic. Compound: Chloro(1,5-cyclooctadiene)copper(I) dimer, is researched, Molecular C16H16Cl2Cu2, CAS is 32717-95-6, about Oxazepine Synthesis by Copper-Catalyzed Intermolecular Cascade Reactions between O-Propargylic Oximes and Dipolarophiles.

Oxazepines I [R1 = n-Pr, cyclohexyl, Ph, 4-F3CC6H4, 4-MeOC6H4; R2 = n-Pr, Me3SiCH2, Ph, 4-MeOC6H4, 4-F3CC6H4; R3 = H, 4-F3CC6H4; R5 = H, R4R6 = C(O)NR7C(O), R7 = H, Me, t-Bu, Ph, etc.; R4 = H, R5 = R6 = MeO2C, i-PrO2C; etc.] were efficiently prepared from O-propargylic oximes II and dipolarophiles R4R5C:CHR6 via copper-catalyzed cascade reactions which proceed through a 2,3-rearrangement, [3 + 2] cycloaddition, and subsequent 1,3-oxygen migration. The process involves the cleavage of C-O and N-O bonds.

Although many compounds look similar to this compound(32717-95-6)Synthetic Route of C16H16Cl2Cu2, numerous studies have shown that this compound(SMILES:C12=C(CCC3=C4CC2)[Cu+]1534[Cl-][Cu+]678(C9=C6CCC7=C8CC9)[Cl-]5), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

Reference:
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N2 | ChemSpider