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分类

• Aryl Boronic Acids, Boronic Acids, Boronic Acids and Derivatives, Chemical Synthesis, Organometallic Reagents, Trisubstituted Aryl Boronic Acids
• {SNA} Aryl Boronic Acids, Boronic Acids, Boronic Acids and Derivatives, Chemical Synthesis, Organometallic Reagents, Trisubstituted Aryl Boronic Acids

相关文献及参考

• 1. A. Adamczyk-Wozniak, et al., , Quantitative determination of the Lewis acidity of phenylboronic catechol esters - Promising anion receptors for polymer electrolytes Inorg. Chem. Commun. 14 , 1753-1755, (2011)
• 2. N. Gavande, et al., , Identification of Benzopyran-4-one Derivatives (Isoflavones) as Positive Modulators of GABAA Receptors ChemMedChem 6 , 1340-1346, (2011)
• 3. W. Jin, et al., , Regio- and Stereoselective Synthesis of Multisubstituted Olefins and Conjugate Dienes by Using a-Oxo Ketene Dithioacetals as the Building Blocks Org. Lett. 13 , 4272-4275, (2011)
• 4. Z. Zhou, et al., , Suzuki cross-coupling reactions of aryl chlorides using [Cl2Pd(COD)]/piperazine derivative under microwave conditions Appl. Organomet. Chem. 25 , 616-619, (2011)
• 5. N. Liu, et al., , Green synthesis of fluorinated biaryl derivatives via thermoregulated ligand/palladium-catalyzed Suzuki reaction J. Organomet. Chem. 696 , 2641-2647, (2011)
• 6. H. Behniafar and M. Sedaghatdoost, , New fluorinated aromatic poly(ether-amide)s derived from 2,2'-bis(3,4,5-trifluorophenyl)-4,4'-diaminodiphenyl ether and various dicarboxylic acids J. Fluor. Chem. 132 , 276-284, (2011)
• Extremely active catalyst for the reaction of carboxylic acids with primary and secondary amines to give the corresponding amides in very high yields: J. Org. Chem., 61, 4196 (1996).
• Extremely active catalyst for the reaction of carboxylic acids with primary and secondary amines to give the corresponding amides in very high yields: J. Org. Chem., 61, 4196 (1996). Also useful in the one-pot synthesis of acyl azides from carboxylic acids and NaN3: Tetrahedron Lett., 43, 9715 (2002). Mediates the mild, one-pot reduction of carboxylic acids to alcohols with NaBH4: Tetrahedron Lett., 44, 3427 (2003).
• For other boronic acid chemistry, see Appendix 5.

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