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In this issue of Chem , Liu and co-workers report an extremely general and mild radical diamination protocol that permits the asymmetric synthesis of vicinal diamines in a highly enantioselective… Click to show full abstract
In this issue of Chem , Liu and co-workers report an extremely general and mild radical diamination protocol that permits the asymmetric synthesis of vicinal diamines in a highly enantioselective manner under a copper(I)/chiral phosphate dual-catalytic system. Notably, this work represents the first asymmetric radical alkene diamination that allows for direct alkylamine incorporation.
Keywords:
diamination;
removing mask;
asymmetric diamination;
mask catalytic;
diamination alkenes;
catalytic asymmetric
Journal Title: Chem
Year Published: 2017
Link to full text (if available)
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Journal Title: Chem
Year Published: 2017
Link to full text (if available)
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recommendations!