Nickel-catalyzed deaminative allenylation of amino acid derivatives: Catalytic activity enhanced by an amide-type NN2 Pincer ligand was written by Zhang, Xingjie;Jiao, Chenchen;Qi, Di;Liu, Xiaopan;Zhang, Zhiguo;Zhang, Guisheng. And the article was included in Organic Letters in 2022.Related Products of 67237-53-0 This article mentions the following:
Herein, we report a general and practical nickel-catalyzed deaminative allenylation of amino acid derivatives with terminal alkynes. The well-designed, electron deficient, and sterically hindered amide-type NN2 Pincer ligand was crucial to the success of this transformation, enabling the coupling to occur under mild conditions with high efficiency. The remarkable features of this chem. are its good scalability, its broad substrate scope, functional group tolerance, and the efficient modification of peptides, drugs, and natural products. In the experiment, the researchers used many compounds, for example, 3-Ethynylthiophene (cas: 67237-53-0Related Products of 67237-53-0).
3-Ethynylthiophene (cas: 67237-53-0) belongs to benzothiophene derivatives. Benzothiophene is used as starting material for the synthesis of bioactive molecules. The core structure is a part of various pharmaceutical substances and natural products. It is also used in the manufacturing of dyes such as thioindigo.Related Products of 67237-53-0
Referemce:
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem