## 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 wi
Synthesis of 13 C labelled unsymmetrically substituted maleic anhydrides
✍ Scribed by L. Breau; M. M. Kayser
- Book ID
- 102368404
- Publisher
- John Wiley and Sons
- Year
- 1988
- Tongue
- French
- Weight
- 398 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Methylmaleic (citraconic) and ethoxymaleic anhydrides labelled with 1 3 C a t C-4, and phenylmaleic anhydride labelled at C-1 were prepared in excellent yields from inexpensive starting materials. methodology described here can be applied i n a synthesis of a variety of substituted maleic anhydrides. The We wish to report highly efficient syntheses o f Carbon-13 labelled maleic anhydrides. into the desired position in the unsyrqnetrically substituted anhydride rings. Two different routes were developed to introduce l 3 C 0 H 0 I -0 RyJ H 0 u 2 R-CHj 3 R=EtO CI 2-Phenylmaleic anhydride -1 labelled at C-1 was prepared as shown in scheme 1. 2-Methylmaleic anhydride 2 and 2-ethoxymaleic anhydride -3 marked 0362-4803/88K)30M1-12~.~ @ 1988 by John Wicy & Sons. Ltd.
📜 SIMILAR VOLUMES
## Abstract The synthesis of tetramethyltetraselenafulvalene (4,4′,5,5′‐tetramethyl Δ^2,2′^‐bis‐1,3‐diselenole) doubly labelled with carbon‐13 in the 2 and 2′‐positions is described. Copyright © 2001 John Wiley & Sons, Ltd.
## Abstract ^13^C‐labelled cinnamonitrile, a compound that possesses both the aromatic functionality of styrene and the nitrile functionality of acrylonitrile has been synthesized in one step using __β__‐bromostyrene and potassium [^13^C]cyanide. The preparation of a target material using ^13^C ‐la