Recent progress in cyclic aryliodonium chemistry: syntheses and applications

X Peng, A Rahim, W Peng, F Jiang, Z Gu… - Chemical …, 2023 - ACS Publications
Hypervalent aryliodoumiums are intensively investigated as arylating agents. They are
excellent surrogates to aryl halides, and moreover they exhibit better reactivity, which allows …

A twist of nature–the significance of atropisomers in biological systems

JE Smyth, NM Butler, PA Keller - Natural product reports, 2015 - pubs.rsc.org
Covering: up to mid-2015 Recently identified natural atropisomeric compounds with
potential medicinal applications are presented. The ability of natural receptors to possess …

New developments of the principle of vinylogy as applied to π-extended enolate-type donor systems

C Curti, L Battistini, A Sartori, F Zanardi - Chemical reviews, 2020 - ACS Publications
The principle of vinylogy states that the electronic effects of a functional group in a molecule
are possibly transmitted to a distal position through interposed conjugated multiple bonds …

Asymmetric total synthesis of polycyclic xanthenes and discovery of a WalK activator active against MRSA

MJ Cheng, YY Wu, H Zeng, TH Zhang, YX Hu… - Nature …, 2024 - nature.com
The development of new antibiotics continues to pose challenges, particularly considering
the growing threat of multidrug-resistant Staphylococcus aureus. Structurally diverse natural …

Recent progress toward developing axial chirality bioactive compounds

Z Wang, L Meng, X Liu, L Zhang, Z Yu, G Wu - European Journal of …, 2022 - Elsevier
Atropisomers are stereoisomers with axial chirality arising from restricted rotation around a
single bond. Lots of representatives of this class of axially chiral compounds exhibit …

Conversion of two stereocenters to one or two chiral axes: atroposelective synthesis of 2, 3-diarylbenzoindoles

YL Hu, Z Wang, H Yang, J Chen, ZB Wu, Y Lei… - Chemical …, 2019 - pubs.rsc.org
Central-to-axial chirality conversion provides efficient access to axially chiral compounds,
and several examples regarding the conversion of one, two or four stereocenters to one axis …

Enantioselective catalysis by chiral isothioureas

J Merad, JM Pons, O Chuzel… - European Journal of …, 2016 - Wiley Online Library
This review covers recent developments relating to organocatalyzed transformations by
chiral isothioureas (ITUs) since their original introduction by Birman in 2006. This class of …

Enantioselective construction of ortho-sulfur- or nitrogen-substituted axially chiral biaryls and asymmetric synthesis of isoplagiochin D

H Yang, W Tang - Nature Communications, 2022 - nature.com
Axially chiral biaryl motifs possessing ortho-heteroatom-substituted functionalities exist
widely in the structures of natural products and have served as foundation for constructing …

Benzoxazine atropisomers: Intrinsic atropisomerization mechanism and conversion to high performance thermosets

K Zhang, Z Shang, CJ Evans, L Han, H Ishida… - …, 2018 - ACS Publications
Atropisomers have inspired chemists and biologists for decades due to their chiral structures
and associated biological properties. However, most of atropisomers reported so far arise in …

Traceless point-to-axial chirality exchange in the atropselective synthesis of biaryls/heterobiaryls

TT Nguyen - Organic & biomolecular chemistry, 2019 - pubs.rsc.org
Traceless point-to-axial chirality exchange is a growing method for the preparation of axially
chiral biaryls/heterobiaryls. During the exchange, stereogenic centers are destroyed and a …