Catalytic Enantioselective Approach to the Stereodivergent Synthesis of (+)-Lasubines I and II was written by Garcia Mancheno, Olga;Gomez Arrayas, Ramon;Adrio, Javier;Carretero, Juan C.. And the article was included in Journal of Organic Chemistry in 2007.Related Products of 10297-05-9 This article mentions the following:
A concise and efficient approach to the stereodivergent synthesis of (+)-lasubines I (I) and II (II) is described. The key common intermediate is a chiral N-sulfonyl 2,3-dihydropyridone obtained by a novel Cu-catalyzed asym. formal aza-Diels-Alder reaction between N-tosyl aldimines and Danishefsky’s diene. In the experiment, the researchers used many compounds, for example, 1-Chloro-4-iodobutane (cas: 10297-05-9Related Products of 10297-05-9).
1-Chloro-4-iodobutane (cas: 10297-05-9) belongs to iodide derivatives. Organic iodides can be alkyl, alkenyl, or alkynyl, and all of them are very reactive toward with many kinds of nucleophiles. In the chemical industry, alkyl iodides serve as excellent alkylating agents and, specifically, methyl iodide is used as a methylating agent in the synthesis of various pharmaceutical drugs.Related Products of 10297-05-9
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com