406482-73-3Relevant articles and documents
Facile synthesis of N-aryl pyrroles via Cu(II)-mediated cross coupling of electron deficient pyrroles and arylboronic acids
Yu, Shu,Saenz, James,Srirangam, Jayaram K.
, p. 1699 - 1702 (2002)
N-arylation of electron-deficient pyrroles has been achieved by cross-coupling with arylboronic acids at room temperature in the presence of stoichiometric amounts of copper(II) acetate. The generality of this reaction has been established with variously substituted pyrroles as well as boronic acids. A key intermediate in the synthesis of a matrix metalloprotease inhibitor has been acheived using this methodology.
1, 3, 5 - cyclohexanetriol - cis - or organic boronic acid-stable siloxy inositol complex and organic synthetic reaction using a reagent art
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Paragraph 0167; 0168; 0184, (2017/06/02)
PROBLEM TO BE SOLVED: To provide a stable ate-type complex of an organoboronic acid as a reagent for organic synthesis reaction; and manufacturing techniques thereof.SOLUTION: A stable ate-type complex of an organoboronic acid with scyllo-inositol or 1,3,5-cis-cyclohexanetriol comprises an anion represented by the specified general formula (I) or (II) as a constituent. In the formula, Rand Reach represent an alkyl group, alkenyl group, alkynyl group, aryl group, heterocyclic group or aralkyl group which may have substituents.
High-quality 2D metal-organic coordination network providing giant cavities within mesoscale domains
Kuehne, Dirk,Klappenberger, Florian,Decker, Regis,Schlickum, Uta,Brune, Harald,et al.
supporting information; scheme or table, p. 3881 - 3883 (2009/08/08)
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