Affiliation:
1. College of Chemistry and Chemical Engineering Qingdao University NingXia Road 308# Qingdao 266071 China
Abstract
AbstractAtropisomers have emerged as important structural scaffolds in natural products, drug design, and asymmetric synthesis. Recently, N−N biaryl atropisomers have drawn increasing interest due to their unique structure and relatively stable axes. However, its asymmetric synthesis remains scarce compared to its well‐developed C−C biaryl analogs. In this concept, we summarize the asymmetric synthesis of N−N biaryl atropisomers including N−N pyrrole−pyrrole, N−N pyrrole−indole, N−N indole−indole, and N−N indole−carbazole, during which a series synthetic strategies are highlighted. Also, a synthetic evolution is briefly reviewed and an outlook of N−N biaryl atropisomers synthesis is offered.
Funder
Taishan Scholar Foundation of Shandong Province
National Natural Science Foundation of China
Natural Science Foundation of Shandong Province
Subject
General Chemistry,Catalysis,Organic Chemistry
Cited by
13 articles.
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