## Abstract A convenient synthesis of triply carbon‐13 labeled 2,2‐dimethyl‐^13^C~2~‐propionitrile‐1‐^13^C is described. The synthetic sequence begins with commercially available propionic acid‐1‐^13^C and methyl iodide‐^13^C with the application of a sequential dianion alkylation. The 2,2‐dimethyl
A novel synthesis of maleic anhydride-1- and -2-13C and its subsequent conversion to labeled maleic hydrazide
✍ Scribed by John M. Patterson; Loren L. Braun; Nabeel F. Haidar; Jack C. Huang; Walter T. Smith Jr.
- Publisher
- John Wiley and Sons
- Year
- 1978
- Tongue
- French
- Weight
- 191 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
Maleic anhydride‐1‐ and 2‐^13^C were synthesized respectively from the available aspartic acid‐4‐ and ‐3‐^13^C by way of the corresponding bromosuccinic acids and their anhydrides. The maleic anhydrides were converted into 1,2‐dihydro‐3,6‐pyrida‐zinedione‐3‐ and ‐4‐^13^C on treatment with aqueous hydrazine sulfate. Nitrogen‐15 labeled 1,2‐dihydro‐3,6‐pyridazinedione was obtained from the latter reaction using hydrazine‐^15^N sulfate.
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