Recommanded Product: 3-Bromo-6-iodo-2-methylpyridineOn September 30, 2016 ,《Povarov reaction, scope and limitations: Preparation of diversely heterocyclic tetrahydro-1H-cyclopenta[c]quinolines》 was published in Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry. The article was written by Ninoa, Patricia; Cabaa, Marta; Aguilarb, Nuria; Terricabrasb, Emma; Albericioc, Fernando; Fernandez, Joan-Carles. The article contains the following contents:
Herein, parallel synthesis of diverse heterocyclic-tetrahydro-1H-cyclopenta[c]quinolines, e.g., I in excellent yields and high endo diastereoselectivity has been described. These compounds are highly functionalized natural product-like tricyclic systems, which may be useful as biol. relevant targets. Fine tuning of the reaction conditions need to be performed depending on the nature and mol. structure of the heterocyclic aromatic carbaldehyde, as well as the choice of the Lewis acid catalyst. Synthesis of the heterocyclic aromatic aldehyde precursors of the Povarov reaction is also described. The experimental part of the paper was very detailed, including the reaction process of 3-Bromo-6-iodo-2-methylpyridine(cas: 1008361-77-0Recommanded Product: 3-Bromo-6-iodo-2-methylpyridine)
3-Bromo-6-iodo-2-methylpyridine(cas: 1008361-77-0) belongs to pyridine. Pyridine-based materials are valued for their optical and physical properties as well as their medical potential. Additionally, pyridine-based natural products continue to be discovered and studied for their properties and to understand their biosynthesis.Recommanded Product: 3-Bromo-6-iodo-2-methylpyridine
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com