Axially chiral compounds have been always considered a laboratory curiosity with rare prospects of being applied in asymmetric synthesis. Things have changed very quickly in the last twenty years when it was understood the important role and the enormous impact that these compounds have in medicinal, biological and material chemistry. The asymmetric synthesis of atropisomers became a rapidly expanding field and recent reports on the development of N-N atropisomers strongly prove how this research field is a hot topic open to new challenges and frontiers of asymmetric synthesis. This review focuses on the recent advances in the enantioselective synthesis of N-N atropisomers highlighting the strategies and breakthroughs to obtain this novel and stimulating atropisomeric framework.

Centonze G., Portolani C., Righi P., Bencivenni G. (2023). Enantioselective Strategies for The Synthesis of N−N Atropisomers. ANGEWANDTE CHEMIE. INTERNATIONAL EDITION, 62(31), 1-15 [10.1002/anie.202303966].

Enantioselective Strategies for The Synthesis of N−N Atropisomers

Centonze G.;Portolani C.;Righi P.;Bencivenni G.
2023

Abstract

Axially chiral compounds have been always considered a laboratory curiosity with rare prospects of being applied in asymmetric synthesis. Things have changed very quickly in the last twenty years when it was understood the important role and the enormous impact that these compounds have in medicinal, biological and material chemistry. The asymmetric synthesis of atropisomers became a rapidly expanding field and recent reports on the development of N-N atropisomers strongly prove how this research field is a hot topic open to new challenges and frontiers of asymmetric synthesis. This review focuses on the recent advances in the enantioselective synthesis of N-N atropisomers highlighting the strategies and breakthroughs to obtain this novel and stimulating atropisomeric framework.
2023
Centonze G., Portolani C., Righi P., Bencivenni G. (2023). Enantioselective Strategies for The Synthesis of N−N Atropisomers. ANGEWANDTE CHEMIE. INTERNATIONAL EDITION, 62(31), 1-15 [10.1002/anie.202303966].
Centonze G.; Portolani C.; Righi P.; Bencivenni G.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/939817
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