Geminal Difunctionalization of Ketones via C─S Bond Insertion of Photogenerated Donor–Donor Diazo Compounds

V Vincent George (Faculty of Chemistry and Pharmacy University of Regensburg Regensburg Germany) A Aryaman Pattanaik (Institute of Organic Chemistry, University Regensburg, Universitätsstr. 31, 93053 Regensburg, Germany) D Daniel Maddox (Compound Synthesis and Management, Discovery Sciences BioPharmaceuticals R&D AstraZeneca Mölndal Sweden) L Lukas M. Sigmund (Molecular AI, Discovery Sciences BioPharmaceuticals R&D AstraZeneca Mölndal Sweden) G Giovanna Mejia (Compound Synthesis and Management, Discovery Sciences BioPharmaceuticals R&D AstraZeneca Mölndal Sweden) S Sara Pahlén (Compound Synthesis and Management, Discovery Sciences BioPharmaceuticals R&D AstraZeneca Mölndal Sweden) S Simon O. Angerer (Faculty of Chemistry and Pharmacy University of Regensburg Regensburg Germany) M Maria Schmoll (Faculty of Chemistry and Pharmacy University of Regensburg Regensburg Germany) L Lisa Marie Schneider (Faculty of Chemistry and Pharmacy University of Regensburg Regensburg Germany) N Nidhal Selmi (Compound Synthesis and Management, Discovery Sciences BioPharmaceuticals R&D AstraZeneca Mölndal Sweden) M Mikhail Kabeshov (Molecular AI, Discovery Sciences BioPharmaceuticals R&D AstraZeneca Mölndal Sweden) G Giulia Bergonzini (Compound Synthesis and Management, Discovery Sciences BioPharmaceuticals R&D AstraZeneca Mölndal Sweden) J Julia Rehbein (Institute of Organic Chemistry, University Regensburg, Universitätsstr. 31, 93053 Regensburg, Germany) B Burkhard König

Abstract

ABSTRACT Geminal difunctionalization of carbonyl‐derived building blocks represents a versatile strategy for the rapid generation of sp 3 ‐rich molecular architectures. In this context, diazo compounds provide a powerful platform for installing two distinct functional groups, yet the reaction space for carbonyl‐derived donor–donor diazo systems remains underdeveloped. Here, we report a metal‐free migratory insertion of diazo compounds into C─S bonds of sulfonyl cyanides, enabling the simultaneous installation of sulfone and nitrile functionalities at a single carbon center. Key to this transformation is the in situ generation of highly reactive diazo intermediates via photochemical decomposition of bench‐stable oxadiazolines derived from ketones. This substantially expands the accessible coupling partner space, previously limited to aldehydes or boronic acids. The reaction exhibits broad functional group, water, and air tolerance, delivers high yields, and provides excellent diastereoselectivity in constrained cyclic systems. Compatibility with both batch and continuous‐flow processing, as well as its application to a realistic medicinal chemistry combinatorial library synthesis, highlights the practical utility of the method.

Article Details

Volume / Issue Vol. 65, Issue 25
Published June 15, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (14)

V

Vincent George

Faculty of Chemistry and Pharmacy University of Regensburg Regensburg Germany

A

Aryaman Pattanaik

Institute of Organic Chemistry, University Regensburg, Universitätsstr. 31, 93053 Regensburg, Germany

D

Daniel Maddox

Compound Synthesis and Management, Discovery Sciences BioPharmaceuticals R&D AstraZeneca Mölndal Sweden

L

Lukas M. Sigmund

Molecular AI, Discovery Sciences BioPharmaceuticals R&D AstraZeneca Mölndal Sweden

G

Giovanna Mejia

Compound Synthesis and Management, Discovery Sciences BioPharmaceuticals R&D AstraZeneca Mölndal Sweden

S

Sara Pahlén

Compound Synthesis and Management, Discovery Sciences BioPharmaceuticals R&D AstraZeneca Mölndal Sweden

S

Simon O. Angerer

Faculty of Chemistry and Pharmacy University of Regensburg Regensburg Germany

M

Maria Schmoll

Faculty of Chemistry and Pharmacy University of Regensburg Regensburg Germany

L

Lisa Marie Schneider

Faculty of Chemistry and Pharmacy University of Regensburg Regensburg Germany

N

Nidhal Selmi

Compound Synthesis and Management, Discovery Sciences BioPharmaceuticals R&D AstraZeneca Mölndal Sweden

M

Mikhail Kabeshov

Molecular AI, Discovery Sciences BioPharmaceuticals R&D AstraZeneca Mölndal Sweden

G

Giulia Bergonzini

Compound Synthesis and Management, Discovery Sciences BioPharmaceuticals R&D AstraZeneca Mölndal Sweden

J

Julia Rehbein

Institute of Organic Chemistry, University Regensburg, Universitätsstr. 31, 93053 Regensburg, Germany

B

Burkhard König