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Updated: Jul 31, 2026

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Facile Preparation of (2Z,4E)-Dienamides by the Olefination of Electron-deficient Alkenes with Allyl Acetate
Published on: June 21, 2017
[C. E. Alken (1909-1986) and the Alken-Prize]
1, Kraichgaustr. 13, 76669, Bad Schönborn, Deutschland. fam@konert-home.de.
Der Urologe. Ausg. A
|May 11, 2016
Summary
Professor C. E. Alken is recognized as a pivotal figure in German urology
Area of Science:
- Urology
- Medical History
Background:
- Details the career trajectory of C. E. Alken, a key figure in post-WWII German urology.
- Highlights his academic appointments, including a teaching assignment in 1948 and the establishment of a Chair of Urology in 1952 at Saarland State University Homburg.
Discussion:
- Explores C. E. Alken's significant contributions to the advancement and autonomy of the field of urology.
- Discusses his influence on the development of urological practices and education in Germany.
Key Insights:
- C. E. Alken's academic progression culminated in an Ordinariat in 1958.
- The establishment of the "Alken-Prize" in his honor underscores his lasting legacy and impact on urology.
Outlook:
- The "Alken-Prize" continues to recognize excellence in urology, perpetuating Alken's influence.
- His career serves as a model for academic and clinical development in the field.
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Structure and Bonding of Alkenes
Olefins, which are unsaturated hydrocarbons containing one or more carbon–carbon double bonds, are broadly divided into alkenes and cycloalkenes. The general chemical formula of an alkene is CnH2n.
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Alkenes like 1-butene and 2-butene exhibit constitutional isomerism, as they differ in the position of the double bond. Further, 2-butene exhibits stereoisomerism and exists as two distinct compounds differing in spatial arrangement.
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Alkenes lose one electron from the unsaturated π bond upon ionization and form stable molecular ions. Further fragmentation of alkenes occurs through three different reaction pathways. The most prominent fragmentation is the cleavage at the allylic position. The resultant allylic carbocation is resonance stabilized. In the mass spectra of terminal alkenes, this fragment appears at a mass-to-charge ratio of 41. In the internal alkenes, where there are two choices of allylic cleavage, the...

