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About the Cover:Enantioselective electrophilic thiolation of alkenes has emerged as a straightforward pathway for the synthesis of chiral sulfides. By this fashion, both the thio group and another valuable functional group can be introduced sim-ultaneously into the parent alkene molecules. This account focuses on the advance on chiral bifunctional chalcogenide-catalyzed enantioselective electrophilic thiofunctionalization of alkenes, which is reported by Jiang and Zhao on page 443.
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About the Cover:Fe-catalyzed borylation of ketones to access tertiary α-hydroxyboronates has been demonstrated by Zhu, Xia, and Liu on page 661. In this transformation, commercially available FeBr2 was used as the catalyst, various aliphatic ketones with different functional groups or steric hinderance have been converted into tertiary α-hydroxyboronates efficiently.
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