Journal article
Direct Methenylation of 4-Alkylpyridines Using Eschenmoser’s Salt
Synlett, Vol.33(19), pp.1902-1906
08/02/2022
DOI: 10.1055/a-1916-5335
Abstract
4-Alkylpyridines are converted to conjugated 1,1-disubstituted alkenyl pyridines (vinyl pyridines) upon treatment with excess ethyl chloroformate, triethylamine, and Eschenmoser’s salt. The reaction proceeds under mild conditions via alkylidene dihydropyridine intermediates
Details
- Title: Subtitle
- Direct Methenylation of 4-Alkylpyridines Using Eschenmoser’s Salt
- Creators
- Grant N. Shivers - University of IowaSoe L. Tun - University of IowaShay L. McLean - University of IowaChris Pigge - The University of Iowa, Department of Chemistry
- Resource Type
- Journal article
- Publication Details
- Synlett, Vol.33(19), pp.1902-1906
- Publisher
- Georg Thieme Verlag KG
- DOI
- 10.1055/a-1916-5335
- ISSN
- 0936-5214
- eISSN
- 1437-2096
- Grant note
- NSF-CHE-2017828 / Division of Chemistry T32-GM008365 / National Institute of General Medical Sciences
- Language
- English
- Date published
- 08/02/2022
- Academic Unit
- Chemistry; Radiology
- Record Identifier
- 9984279157702771
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