Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Article, Research Support, Non-U.S. Gov’t, Organic Letters called Anti-Selective Direct Catalytic Asymmetric Aldol Reaction of Thiolactams, Author is Sureshkumar, Devarajulu; Kawato, Yuji; Iwata, Mitsutaka; Kumagai, Naoya; Shibasaki, Masakatsu, which mentions a compound: 75732-01-3, SMILESS is [Cu]C1=C(C)C=C(C)C=C1C, Molecular C9H11Cu, Product Details of 75732-01-3.
An anti-selective direct catalytic asym. aldol reaction of thiolactams is described. A soft Lewis acid/hard Bronsted base cooperative catalyst comprised of mesitylcopper/(R,R)-Ph-BPE exhibited high catalytic performance to produce an anti-aldol product with high stereoselectivity. The highly chemoselective nature of the present catalysis allows for the use of enolizable aldehydes as aldol acceptors. The diverse transformations of the thiolactam moiety highlight the synthetic utility of the present anti-aldol protocol.
Although many compounds look similar to this compound(75732-01-3)Product Details of 75732-01-3, numerous studies have shown that this compound(SMILES:[Cu]C1=C(C)C=C(C)C=C1C), has unique advantages. If you want to know more about similar compounds, you can read my other articles.
Reference:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com