Willard M. Welch, Catherine E. Hanau, William M. Whalen
Abstract
All articles of this category The dianion prepared from 3-bromo-1 H -indazole and alkyllithium bases reacts with a variety of electrophiles to give the corresponding 3-monosubstituted 1 H -indazole derivatives in moderate yields. This procedure is more general and shorter than earlier methods.
OpenAlex reports 29 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
All articles of this category The dianion prepared from 3-bromo-1 H -indazole and alkyllithium bases reacts with a variety of electrophiles to give the corresponding 3-monosubstituted 1 H -indazole derivatives in moderate yields. This procedure is more general and shorter than earlier methods.
Key concepts: Indazole, Chemistry, Electrophile, Combinatorial chemistry, Medicinal chemistry, Organic chemistry, Catalysis