Narasimhan, S and Vithayathil, PJ (1986) A new reaction of o-benzoquinone with N-acetyl-DL-tryptophan (a 3-substituted indole) and characterization of the product. In: Indian Journal of Biochemistry & Biophysics, 23 (4). pp. 215-219.
Full text not available from this repository. (Request a copy)Abstract
o-Benzoquinone reacts with 3-substituted indoles under acidic conditions to give products having distinct UV characteristics. The o-benzoquinone derivation of N-acetyl-DL-tryptophan prepared in the presence of HCl was chromatography homogeneous and had 1 equiv of Cl- per molecular Potentiometric titrn. showed the presence of C:O and OH groups. Based on NMR, IR, and elementary analysis, structure I was assigned to the derivation in which the o-benzoquinone moiety is incorporated at the indole N atom of N-acetyl-DL-tryptophan.
| Item Type: | Journal Article |
|---|---|
| Additional Information: | Copyright of this article belongs to National Institute of Science Communication and Information Resources |
| Department/Centre: | Division of Biological Sciences > Biochemistry |
| Date Deposited: | 28 Apr 2008 |
| Last Modified: | 27 Aug 2008 13:20 |
| URI: | http://eprints.iisc.ernet.in/id/eprint/13766 |
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