Synthesis of Chiral δ-Aminoboronic Esters by Enantioselec- tive Hydrogenation of 1,2-Azaborines

24 September 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

We describe herein an iridium-catalyzed highly diastereo- and enantioselective hydrogenation of 1,2-azaborines ac- cessing δ-aminoboronic esters of potential biological importance. This method represents the first enantioselective hydrogenation of boron-containing heteroarene and features a diverse substitution pattern and wide scope. The synthetic utility of our method was demonstrated by the synthesis of (–)-Phenibut and the formal synthesis of (+)-3-PPP and Fluvirucinine A1.

Keywords

Azaborines
Enantioselective Hydrogenation
Aminoboronic Esters

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