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Anion-Mediated, Stereospecific Synthesis of Secondary and Tertiary Cyclopropylboronates from Chiral Epoxides and <i>gem</i>-Diborylalkanes

G.N. Kim, Minjae Kim, Changsu Ryu, J.‐K. CHOI, Seung Hwan Cho

2023Organic Letters27 citationsDOI

Abstract

We report a transition-metal-free deborylative cyclization approach to synthesize enantioenriched secondary and tertiary cyclopropylboronates using γ-phosphate-containing gem -diborylalkanes derived from chiral epoxides and gem -diborylalkanes. Our method enables the synthesis of a broad range of enantioenriched secondary and tertiary cyclopropylboronates in good yields with excellent stereospecificity. We demonstrate the versatility of our approach by performing a gram-scale reaction. We also show that the enantioenriched tertiary cyclopropylboronates can be transformed into a wide array of enantioenriched cyclopropane derivatives in a stereospecific boron-group transformation.

Topics & Concepts

StereospecificityChemistryCyclopropaneTertiary careBoronCombinatorial chemistryRing (chemistry)Organic chemistryStereochemistryCatalysisMedicineFamily medicineOrganoboron and organosilicon chemistryCyclopropane Reaction MechanismsCatalytic Cross-Coupling Reactions
Anion-Mediated, Stereospecific Synthesis of Secondary and Tertiary Cyclopropylboronates from Chiral Epoxides and <i>gem</i>-Diborylalkanes | Litcius