Efficient Asymmetric Synthesis of Biologically Important Tryptophan Analogues via a Palladium-Mediated Heteroannulation Reaction was written by Ma, Chunrong;Liu, Xiaoxiang;Li, Xiaoyan;Flippen-Anderson, Judith;Yu, Shu;Cook, James M.. And the article was included in Journal of Organic Chemistry in 2001.HPLC of Formula: 220185-63-7 This article mentions the following:
A novel and concise synthesis of optically active tryptophan derivatives was developed via a palladium-catalyzed heteroannulation reaction of substituted o-iodoanilines with an internal alkyne. The required internal alkyne I was prepared in greater than 96% diastereomeric excess via alkylation of the Schollkopf chiral auxiliary, 3,6-diethoxy-2R-isopropyl-2,5-dihydropyrazine with Me3SiCCCH2OP(:O)(OPh)2. Similarly, alkyne II was obtained from the alkylation of 3,6-diethoxy-2S-isopropyl-2,5-dihydropyrazine by TMSCCCH2OP(:O)(OPh)2. I was used as an intermediate in the palladium-catalyzed heteroannulation reaction to afford
4,5-Dichloro-2-iodoaniline (cas: 220185-63-7) belongs to iodide derivatives. In general, organic iodides are light-sensitive and turn yellow during storage, owing to the formation of iodine. Polyiodoorganic compounds are sometimes employed as X-ray contrast agents, in fluoroscopy, a type of medical imaging. This application exploits the X-ray absorbing ability of the heavy iodine nucleus.HPLC of Formula: 220185-63-7
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com