Efficient Synthesis of Chiral ProTides through Copper Catalysis
A new study introduces a novel method for the stereoselective synthesis of chiral phosphates in ProTide nucleoside analogues.
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A new study introduces a novel method for the stereoselective synthesis of chiral phosphates in ProTide nucleoside analogues.
The access and the usage of anti-Bredt type olefins as intermediates are described in a new study in Science.
The construction of quaternary centers via C-C bond formation is a significant challenge, but a new method reported in JACS, provides a promising approach to accessing these …