Desymmetrization and Atroposelective Cobalt Catalyzed C–H Annulation of Phosphinic Amides with Ynamides

Metal-catalyzed asymmetric C-H annulation enables enantioselective synthesis from simple precursors, but methods that simultaneously generate multiple stereogenic elements in a single step remain rare. We report the first Co(II)/Salox-catalyzed desymmetrizing atroposelective C-H annulation of phosphinic amides with ynamides, simultaneously generating a P-stereogenic center and C-C/C-N chiral axes in high yield and enantioselectivity (up to 87% yield, >99% ee). Notably, this catalytic system shows a substrate-dependent stereochemical outcome at the C-N axis, which is significant and nontrivial. DFT calculations are consistent with the experimentally observed stereochemical outcome and support a plausible model for stereocontrol. This work provides a valuable platform for the asymmetric synthesis of structurally and stereochemically complex organophosphorus compounds.

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Publication Details

Journal
Organic Letters
Published
2026-03-02
DOI
https://doi.org/10.1021/acs.orglett.6c00278
Primary Topic
Axial and Atropisomeric Chirality Synthesis
Type
article
Field-Weighted Citation Impact
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article

Desymmetrization and Atroposelective Cobalt Catalyzed C–H Annulation of Phosphinic Amides with Ynamides

Abid Allah Mohammed Ali, Somratan Sau, Akhila K. Sahoo, Vincent Gandon et al.
Organic Letters
Axial and Atropisomeric Chirality Synthesis
article

Desymmetrization and Atroposelective Cobalt Catalyzed C–H Annulation of Phosphinic Amides with Ynamides

Abid Allah Mohammed Ali, Somratan Sau, Akhila K. Sahoo, Vincent Gandon, Paushali Naskar, Koushik Pradhan
article en

Abstract

Metal-catalyzed asymmetric C-H annulation enables enantioselective synthesis from simple precursors, but methods that simultaneously generate multiple stereogenic elements in a single step remain rare. We report the first Co(II)/Salox-catalyzed desymmetrizing atroposelective C-H annulation of phosphinic amides with ynamides, simultaneously generating a P-stereogenic center and C-C/C-N chiral axes in high yield and enantioselectivity (up to 87% yield, >99% ee). Notably, this catalytic system shows a substrate-dependent stereochemical outcome at the C-N axis, which is significant and nontrivial. DFT calculations are consistent with the experimentally observed stereochemical outcome and support a plausible model for stereocontrol. This work provides a valuable platform for the asymmetric synthesis of structurally and stereochemically complex organophosphorus compounds.

Organic LettersVol. 28(10)
Université Paris-Saclay (FR), University of Hyderabad (IN), Institut de Chimie Moléculaire et des Matériaux d'Orsay (FR)
Openalex Percentile: Top 37%
Axial and Atropisomeric Chirality Synthesis
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