From Enantioenriched Donor‐Acceptor Cyclopropylcarbinols to Axially Chiral Arylnaphthalenes through Aryldihydronaphthalenes: Central‐to‐Axial Chirality Exchange
Author:
Affiliation:
1. Department of Applied Chemistry, Faculty of Textile Science and Technology Shinshu University Tokida 3-15-1 Ueda Nagano 386–8567 Japan
Funder
Shinshu University
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejoc.202101213
Reference146 articles.
1. For recent reviews see:
2. Construction of Axially Chiral Compounds via Asymmetric Organocatalysis
3. Catalyst-Controlled Stereoselective Synthesis of Atropisomers
4. Recent advances in the synthesis of axially chiral biarylsviatransition metal-catalysed asymmetric C–H functionalization
5. Enantioselective Synthesis of Atropisomers with Multiple Stereogenic Axes
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1. Enantioselective Synthesis of Atropisomers by Oxidative Aromatization with Central-to-Axial Conversion of Chirality;Molecules;2023-03-31
2. Atroposelective Synthesis of C-C Axially Chiral Compounds via Mono- and Dinuclear Vanadium Catalysis br;ACCOUNTS CHEM RES;2022
3. Atroposelective Synthesis of C–C Axially Chiral Compounds via Mono- and Dinuclear Vanadium Catalysis;Accounts of Chemical Research;2022-10-07
4. Asymmetric Total Synthesis of a Bioactive Lignanamide Using a 5‐ endo ‐ tet ‐Type Cyclization of Activated Cyclopropylcarbinols and Synthetic Support for the Reaction Mechanism;European Journal of Organic Chemistry;2022-07-28
5. Recent advances in the catalytic asymmetric construction of atropisomers by central-to-axial chirality transfer;Organic Chemistry Frontiers;2022
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