Bischler-Napieralski Reaction

The Bischler–Napieralski Reaction refers to an intramolecular electrophilic substitution reaction in which β-aryl ethylamides undergo cyclization in the presence of chlorinating reagents to form 1,2-dihydroisoquinoline derivatives. This reaction was first discovered in 1893 by German chemist August Bischler and Swiss chemist Bernard Napieralski during their research on alkaloids. It is...

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Bergman Cyclization

Bergman Cyclization is a reaction in which enediyne compounds undergo thermal or photochemical cyclization in the presence of a hydrogen donor (such as 1,4-cyclohexadiene) to form substituted benzene derivatives. The reaction is named after American chemist Robert G. Bergman. Due to the limited range of suitable substrates and stringent conditions,...

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Blanc chloromethylation

Blanc Chloromethylation refers to the reaction in which aromatic compounds react with formaldehyde and hydrogen chloride in the presence of anhydrous zinc chloride as a catalyst to form chloromethylated aromatic compounds. This reaction was first reported by Grassi-Cristaldi and Maselli in 1898 and later expanded by Blanc in 1923, hence...

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Blaise Reaction

Blaise Reaction refers to the reaction between a nitrile and an α-bromoester in the presence of zinc to form β-enamino esters or β-keto esters. It was first reported by Edmond Blaise in 1901 and is named after him. The Blaise reaction has certain drawbacks, such as a narrow substrate scope...

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Bohlmann–Rahtz Pyridine Synthesis

Bohlmann-Rahtz Pyridine Synthesis is an efficient two-step method for obtaining substituted pyridines. In the first step, an enamine condenses with an alkynone to form an aminodiene intermediate. This is followed by a thermally induced E/Z isomerization, and then a cyclodehydration reaction occurs, forming a 2,3,6-trisubstituted pyridine. The reaction was first...

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Cadiot-Chodkiewicz Coupling

Cadiot-Chodkiewicz Coupling Reaction The Cadiot-Chodkiewicz coupling refers to the catalytic coupling of a terminal alkyne with a haloalkyne in the presence of a copper(I) salt (e.g., cuprous chloride or cuprous bromide) and a base to yield a diyne derivative. This reaction was discovered by Paul Cadiot and W. Chodkiewicz and is named after them. The Cadiot-Chodkiewicz...

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