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- W4365133669 abstract "Abstract This short review summarizes our laboratory’s development of benzylboronic esters as nucleophiles. Activation of the benzylboronic ester is achieved by irreversible coordination of an alkyllithium Lewis base to form a nucleophilic benzylboronate. This boronate was found to react with aldehydes, imines, ketones, and alkyl bromides. A copper catalyst was employed in reactions of the boronate with epoxides and aziridines. 1 Introduction 2 1,2-Additions 3 Additions to sp3 Electrophiles 4 Conclusion and Outlook" @default.
- W4365133669 created "2023-04-13" @default.
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- W4365133669 date "2023-04-12" @default.
- W4365133669 modified "2023-10-05" @default.
- W4365133669 title "Reactions of Benzylboronate Nucleophiles" @default.
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- W4365133669 doi "https://doi.org/10.1055/a-2072-2754" @default.
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