New method of kinetic resolution of axially chiral biaryl compounds using a sugar template.

1995 ◽  
Vol 60 (16) ◽  
pp. 4968-4969 ◽  
Author(s):  
Toshiyuki Itoh ◽  
Jun-ichi Chika
2014 ◽  
Vol 126 (44) ◽  
pp. 12012-12015 ◽  
Author(s):  
Gaoyuan Ma ◽  
Jun Deng ◽  
Mukund P. Sibi

ChemInform ◽  
2016 ◽  
Vol 47 (18) ◽  
Author(s):  
Pauline Loxq ◽  
Eric Manoury ◽  
Rinaldo Poli ◽  
Eric Deydier ◽  
Agnes Labande

ACS Catalysis ◽  
2021 ◽  
pp. 4117-4124
Author(s):  
José A. Carmona ◽  
Carlos Rodríguez-Franco ◽  
Joaquín López-Serrano ◽  
Abel Ros ◽  
Javier Iglesias-Sigüenza ◽  
...  

Synthesis ◽  
2020 ◽  
Vol 52 (17) ◽  
pp. 2450-2468
Author(s):  
Vasco Corti ◽  
Giulio Bertuzzi

A perspective on the literature dealing with the organocatalytic asymmetric preparation of axially chiral N-heterocycles is provided. A particular focus is devoted to rationalize the synthetic strategies employed in each case. Moreover, specific classes of organocatalysts are shown to stand out as privileged motives for the stereoselective preparation of such synthetically challenging molecular architectures. Finally, an overview of the main trends in the field is given.1 Introduction2 Five-Membered Rings2.1 Arylation2.2 Dynamic Kinetic Resolution2.3 Ring Construction2.4 Central-to-Axial Chirality Conversion and Chirality Transfer2.5 Desymmetrization3 Six-Membered Rings3.1 Desymmetrization3.2 (Dynamic) Kinetic Resolution3.3 Ring Construction3.4 Central-to-Axial Chirality Conversion4 Conclusion


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