Liquizald─Thermally Stable <i>N</i>-Nitrosamine Precursor for Diazomethane-Reference-Cited by-同舟云学术

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Liquizald─Thermally Stable N-Nitrosamine Precursor for Diazomethane

Published:2024-01-26 Issue:2 Volume:28 Page:597-608
ISSN:1083-6160
Container-title:Organic Process Research & Development
language:en
Short-container-title:Org. Process Res. Dev.

Author:

Horvath-Gerber Filip¹^ORCID,Ohlig Dominik²,Hii King Kuok Mimi³^ORCID,Deadman Benjamin⁴,Attrill Robin P.¹,Hellgardt Klaus¹

Affiliation:

1. Department of Chemical Engineering, Imperial College London, London SW7 2AZ, U.K.

2. BASF SE, Ludwigshafen am Rhein 67063, Germany

3. Department of Chemistry, Imperial College London, London W12 7TA, U.K.

4. Centre for Rapid Online Analysis of Reactions (ROAR), Imperial College London, London W12 7TA, U.K.

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.oprd.3c00456

Reference67 articles.

1. Ueber Diazomethan

2. The synthetic versatility of the Tiffeneau–Demjanov chemistry in homologation tactics

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1. Synthesis of Secondary Boronates via Deaminative Cross‐Coupling of Alkyl Nitroso Carbamates and Boronic Acids;Angewandte Chemie International Edition;2024-08-02

2. Highlights of the Recent Patent Literature: Continuous Chemistry in the Pharmaceutical Industry;Organic Process Research & Development;2024-01-26

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