ESR Spectra of Some Amino Acid Derivatives of Semiquinone Anions
✍ Scribed by Frank R. Hewgill; Ulrike Höfler; Richard C. Power; Hartmut B. Stegmann
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 395 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Reaction of the n-butyl esters of alanine and leucine with both tert-butyl-1,4-benzoquinone and 1,4-naphthoquinone gave the corresponding N-substituted quinones. Substitution at both C-5 and C-6 was observed with 2-tert-butyl-1,4-benzoquinone, but C-6 substitution predominated. Reduction of the latter isomers and of the naphthoquinones gave ESR spectra to which splitting constants were assigned with the help of ENDOR spectroscopy and selective deuteration.
📜 SIMILAR VOLUMES
I n most cases silicon-nitrogen compounds are readily cleaved by Lewis acids at the Si--N bondL21. Treatment of bisftri-methylsily1)diimine 131 should thus lead to a synthesis of new derivatives of diimine. R--N=N-R:
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