Isothiourea‐Catalysed Acylative Kinetic and Dynamic Kinetic Resolution of Planar Chiral Paracyclophanols

Abstract The development of synthetic methods for the catalytic enantioselective preparation of planar chiral paracyclophane derivatives is of considerable interest to the synthetic community. To date, relatively few successful and effective organocatalytic approaches to this molecular class have been reported. This manuscript describes effective isothiourea catalysed acylative kinetic (KR) and dynamic kinetic resolution (DKR) approaches to the generation of a range of planar chiral paracyclophane macrocycles with excellent levels of enantioselectivity. Effective KR of configurationally stable planar chiral paracyclophanols with 12‐ and 13‐membered ansa ‐chains is demonstrated (6 examples, s = up to 50) using 5 mol% of the isothiourea ( R )‐BTM and isobutyric anhydride. Application to configurationally labile macrocyclic phenols with 14 to 18‐membered ansa ‐chains allows their effective acylative DKR, generating the desired products with excellent enantioselectivity (25 examples, up to 95% yield and 98:2 er).

Authors

Institutions

Publication Details

Journal
Angewandte Chemie
Published
2025-05-20
DOI
https://doi.org/10.1002/ange.202507126
Primary Topic
Synthesis and Properties of Aromatic Compounds
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Isothiourea‐Catalysed Acylative Kinetic and Dynamic Kinetic Resolution of Planar Chiral Paracyclophanols

Kevin Kasten, Andrew D. Smith, David B. Cordes, Aidan P. McKay et al.
Angewandte Chemie
Synthesis and Properties of Aromatic Compounds
article

Isothiourea‐Catalysed Acylative Kinetic and Dynamic Kinetic Resolution of Planar Chiral Paracyclophanols

Kevin Kasten, Andrew D. Smith, David B. Cordes, Aidan P. McKay, Zhanyu Zhou
article en

Abstract

Abstract The development of synthetic methods for the catalytic enantioselective preparation of planar chiral paracyclophane derivatives is of considerable interest to the synthetic community. To date, relatively few successful and effective organocatalytic approaches to this molecular class have been reported. This manuscript describes effective isothiourea catalysed acylative kinetic (KR) and dynamic kinetic resolution (DKR) approaches to the generation of a range of planar chiral paracyclophane macrocycles with excellent levels of enantioselectivity. Effective KR of configurationally stable planar chiral paracyclophanols with 12‐ and 13‐membered ansa ‐chains is demonstrated (6 examples, s = up to 50) using 5 mol% of the isothiourea ( R )‐BTM and isobutyric anhydride. Application to configurationally labile macrocyclic phenols with 14 to 18‐membered ansa ‐chains allows their effective acylative DKR, generating the desired products with excellent enantioselectivity (25 examples, up to 95% yield and 98:2 er).

Angewandte ChemieVol. 137(31)
University of St Andrews (GB)
Openalex Percentile: Top 92%
Synthesis and Properties of Aromatic Compounds
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.