## Abstract Trans‐[13,14‐^14^C~2~]‐Retinoic acid has been synthesized by condensation of β‐ionylideneacetaldehyde and ^14^C‐labeled methyl senecioate in the presence of potassium amide in ether. A convenient synthesis of the key intermediate, methyl (diethoxyphosphinyl)‐[2‐^14^C]acetate, is also de
Synthesis of methyl trans-(10- 14C)-retinoate and trans-(10- 14C)-retinol
✍ Scribed by J. D. Bu'Lock; S. A. Quarrie; D. A. Taylor
- Publisher
- John Wiley and Sons
- Year
- 1973
- Tongue
- French
- Weight
- 353 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The preparation of the title compunds, using β‐ionone, is accomplished in fair overall radiochemical yield from (2‐^14^C) bromacetic acid, in 7 and 8 steps respectively. The sequence utilises ylid reactions of the phosphonoacetate derived from bromacetic ester, and is also capable of the introduction of label at C‐14.
📜 SIMILAR VOLUMES
A synthetic procedure for producing all trans [3A4C]menaquinone-4 is described The radiolabe is introduced using ethyl [3-'4C]acetoacetate as shown in the scheme. The final product has high chemical and radiochemical purity with a specific activity of 669 MBS/mnol. The overall radiochemical yield is
## Abstract The synthesis of the title compound (5) is described. Treatment of mitomycin C with sodium methoxide gave decarbamoyl mitomycin C (2). Reaction with acetic anhydride in methanol yielded N1a‐acetyl‐mitomycin C (3). Treatment with [^14^C]phosgene in the presence of N,N‐dimethylaniline yie
## Abstract Pentylenetrazole‐10‐^14^C was synthesized by reacting hydrazoic acid with cyclohexanone‐1‐^14^C. Purification was carried out using sublimation and thick layer chromatography. Proof of radiochemical purity was determined using thin layer chromatography and autoradiography. The specific