Cronk, W. Cole published the artcileIntramolecular Photoassisted Cycloadditions of Azaxylylenes and Postphotochemical Capstone Modifications via Suzuki Coupling Provide Access to Complex Polyheterocyclic Biaryls, Application In Synthesis of 53279-83-7, the publication is Journal of Organic Chemistry (2014), 79(3), 1235-1246, database is CAplus and MEDLINE.
Modular preassembly of azaxylylene photoprecursors, halogen-substituted in the aromatic ring, their intramol. [4 + 4] or [4 + 2] cycloadditions to tethered unsaturated pendants, and subsequent postphotochem. capstone modification of the primary photoproducts via Suzuki coupling provides rapid access to diverse biaryls of unprecedented topol. [e.g., I â?(II + III) â?(IV + V)]. This synthetic sequence allows for rapid growth of mol. complexity and is well aligned with methodol. of diversity-oriented synthesis.
Journal of Organic Chemistry published new progress about 53279-83-7. 53279-83-7 belongs to iodides-buliding-blocks, auxiliary class Iodide,Amine,Benzene,Alcohol, name is (2-Amino-5-iodophenyl)methanol, and the molecular formula is C7H8INO, Application In Synthesis of 53279-83-7.
Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com