1. Academic Validation
  2. Asymmetric Synthesis of Nortropanes via Rh-Catalyzed Allylic Arylation

Asymmetric Synthesis of Nortropanes via Rh-Catalyzed Allylic Arylation

  • ACS Catal. 2022 Aug 5;12(15):8995-9002. doi: 10.1021/acscatal.2c02259.
Yan Zhang 1 F Wieland Goetzke 1 Kirsten E Christensen 1 Stephen P Fletcher 1
Affiliations

Affiliation

  • 1 Department of Chemistry, Chemistry Research Laboratory, University of Oxford, 12 Mansfield Road, Oxford OX1 3TA, United Kingdom.
Abstract

Tropane derivatives are extensively used in medicine, but catalytic asymmetric methods for their synthesis are underexplored. Here, we report Rh-catalyzed asymmetric Suzuki-Miyaura-type cross-coupling reactions between a racemic N-Boc-nortropane-derived allylic chloride and (hetero)aryl boronic esters. The reaction proceeds via an unexpected kinetic resolution, and the resolved enantiopure allyl chloride can undergo highly enantiospecific reactions with N-, O-, and S-containing nucleophiles. The method was applied in a highly stereoselective formal synthesis of YZJ-1139(1), a potential insomnia treatment that recently completed Phase II clinical trials. Our report represents an asymmetric catalytic method for the synthesis of YZJ-1139(1) and related compounds.

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