## Abstract Perdeuterio‐N‐(1‐oxyl‐2,2,6,6‐tetramethyl‐4‐piperidinyl)‐maleimide has been prepared to improve sensitivity and resolution in its ESR spectrum. The synthesis involved modifications of procedures known for the corresponding protonated analog. Spectral data are presented for the product t
Stable isotope substituted spin labels. 2. An improved synthesis of perdeuterio-15N-(1-oxyl-2,2,6,6-tetramethyl- 4-piperidinyl)maleimide
✍ Scribed by Barbara A. Bates; Michael E. Johnson; Bruce L. Currie
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- French
- Weight
- 267 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Stable isotope substituted spin labels increase t&e resolution and sensitivity of EPR measurements. An improved synthesis of N-(l-oxy1-2,2,6,6-tetramethyl-4-piperidiny1)maleimide has been devised and utilized. This improved synthesis is accomplished in five steps instead of the normally required seven or more.
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Spin l a b e l e d drugs can be u t i l i z e d f o r innnunoassays and determining t h e f r a c t i o n o f f r e e drug i n serum. To improve t h e sensit i v i t y we have synthesized t r i a c e t ~n a m i n e -~~N -d ~? by c y c l i z a t i o n o f phorone-d14 w i t h l5ND,. Phorone-d was obta