Chiral medium-sized rings beyond central chirality

Nature Reviews Chemistry, Published online: 14 July 2025; doi:10.1038/s41570-025-00735-1Chiral medium-sized rings (MSRs) beyond central chirality, with unique rigid–flexible features, show broad potential. This Review highlights progress in the enantioselective synthesis of axial, inherent and planar chiral MSRs, and it critically assesses key synthetic strategies.

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Total Synthesis of Chartelline C

Chartellines are cytotoxic marine alkaloids that were isolated in the late 1980s. Their unique, heavily oxidized structures, comprising a spirocyclic β-lactam, a halogenated indolenine, a chloroenamide, and a 2-haloimidazole, have motivated extensive efforts toward their synthesis. However, only a single synthesis of any chartelline has been reported in the nearly 40 years since their isolation. Here, we describe a route to chartelline C (3) from the macrolactam 21, an intermediate we employed en route to the related securine and securamine alkaloids. The key challenges in converting macrolactam 21 to chartelline C (3) involve stereocontrolled construction of the C2–C3 enamide, isomerization of the trans-C10–C11 alkene, formation of the strained spirocyclic β-lactam, and chlorination of the enamide. Each of these challenges was addressed by an unconventional approach. The macrolactam 21 was converted to cis-enamide (2Z,10E)-24 by in situ masking of the C12 ketone, followed by stereoselective acid-catalyzed elimination of the C2 carbinolamide. The C10–C11 trans-alkene was isomerized by a photolytic process; control experiments suggest that this isomerization occurs by energy transfer. The β-lactam was constructed by a solid-state reaction involving the adsorption of the bromoindolenine 26 onto activated basic alumina. Late-stage enamide chlorination, which had been an obstacle in prior approaches, was accomplished by a novel photoredox-mediated halogenation. These latter studies suggest that N-haloanomeric amides and N-haloguanidines may act as halogen atom transfer agents under thermal or photolytic conditions. Finally, we show that chartelline C (3) reacts with sulfur-based nucleophiles, suggesting that further studies of their biological activity may be warranted.

pubs.acs.org

g-xTB: A General-Purpose Extended Tight-Binding Electronic Structure Method For the Elements H to Lr (Z=1–103)

We present g-xTB, a next-generation semi-empirical electronic structure method derived from tight-binding (TB) approximations to Kohn–Sham density functional theory (KS-DFT). Designed to bridge the ga...

chemrxiv.org

Degradative Alcohol Functionalization by Titanocene Photocatalysis

Organotitanium complexes are scarcely employed in photocatalytic reactions despite their robust ligand-to-metal charge-transfer photo-chemistry. Herein, we describe the development of titanocene pho-t...

chemrxiv.org

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doi.org

PhD scholarship in Organic Chemistry and Enantioselective Homogeneous Catalysis - DTU Chemistry

A fully-funded 3-year PhD position in organic chemistry, C-H functionalization, and homogeneous enantioselective metal catalysis under the supervision of Associate Professor Søren Kramer is available ...

efzu.fa.em2.oraclecloud.com

Software Update: The ORCA Program System—Version 6.0

This article describes the philosophy behind- and new features in the ORCA quantum chemistry program suite, version 6.0.

wires.onlinelibrary.wiley.com

Opinion | The Uncertain Fate of the Young American Scientist (Gift Article)

Young researchers are choosing between staying in science and staying in the United States.

nytimes.com