用于Suzuki-type交叉偶联反应。 应用 4-氰基苯硼酸可作为反应物参与： 钯催化的水相Suzuki-Miyaura交叉偶联。 钌催化无环胺的苄基 sp3 碳与芳基硼酸盐的直接芳基化。 无配体铜催化的硝基芳烃与芳基硼酸的偶联。 高氯酸铁促进富勒烯与各种芳基硼酸的反应，得到富勒烯基硼酸酯。 不含磷的 Suzuki-Miyaura 交叉偶联。 Palladacycles 作为与烯丙基钯中间体的多组分反应的有效催化剂。 Cu催化的硫醇Chan-Lam S-芳基化。 在改性的 Suzuki 和 Still 交叉偶联反应下，与铜催化的区域选择性交叉偶联反应。 存在碳酸二甲酯溶剂的情况下的无金属联芳基偶联反应。 不存在碱的情况下与五价三芳基二乙酸锑的Suzuki 交叉偶联反应。 它还可用于制备： 喜巴辛类似物，作为凝血酶受体拮抗剂和潜在的抗血小板药物。 三磺化杯芳烃上限磺胺嘧啶，以及具有三甲基赖氨酸表观遗传标记的络合物。 抗疟疾化合物，通过 Suzuki 交叉偶联反应制得。 脱氧尿苷衍生物 作为反应物，参与以下反应： 氧化羟基化 三氟甲基化 1,4-加成反应 合成以下抑制剂的前体，例如： Tpl2 激酶抑制剂 用于治疗疼痛的 P2X7 拮抗剂 4-Cyanophenylboronic acid can be used as a reactant in: Palladium-catalyzed Suzuki-Miyaura cross-coupling in water. Ruthenium catalyzed direct arylation of benzylic sp3 carbons of acyclic amines with arylboronates. Ligand-free copper-catalyzed coupling of nitro arenes with arylboronic acids. Ferric perchlorate-promoted reaction of fullerenes with various arylboronic acids to give fullerenyl boronic esters. Phosphine-free Suzuki-Miyaura cross-coupling. Palladacycles as effective catalysts for multicomponent reaction with allylpalladium-intermediates. Chan-Lam-type Cu-catalyzed S-arylation of thiols. Regioselective cross-coupling reactions under modfied Suzuki and Still cross-coupling reactions with copper catalysis. Metal-free biaryl coupling reaction in the presence of dimethyl carbonate as a solvent. Suzuki-type cross-coupling reaction with pentavalent triarylantimony diacetates in the absence of a base. It can also be used to prepare: Himbacine analogs as thrombin receptor antagonists and potential antiplatelet agents. Trisulfonated calixarene upper-rim sulfonamido and their complexation with trimethyllysine epigenetic mark. Antimalarial compounds via Suzuki cross-coupling. Deoxyuridine derivatives. Reactant involved in: Oxidative hydroxylation Trifluoromethylation 1,4-Addition reactions Precursor in the synthesis of inhibitors such as: Tpl2 kinase inhibitors P2X7 antagonists used in the treatment of pain