## Abstract All‐__trans__‐Retinoic acid [11,12‐^3^H(N)] was photochemically isomerized using a fluorescent source to afford a mixture of isomeric retinoic acids, from which 9‐__cis__‐retinoic acid[11,12‐^3^H(N)] was isolated by reversed‐phase HPLC. The identity of 9‐__cis__‐retinoic acid [11, 12‐^3
A preparation of high specific activity [11,12-3H]-9-cis-retinoic acid
✍ Scribed by Jotham W. Coe; Calvin R. Hawes; Patrick Towers
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- French
- Weight
- 429 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
A selective total synthesis of [11,12‐^3^H]‐9‐cis‐retinoic acid 1 at a specific activity of 46 Ci/mmole is described. The alkyne 4, efficiently prepared in two steps from readily available starting materials, was partially reduced to 9,11‐di‐cis‐retinoic acid 3 with both deuterium and tritium gas. Selective isomerization of 3 to 1 is discussed, as well as non‐selective direct conversions of 4 to 1.
📜 SIMILAR VOLUMES
A method is described by which tritium-labeled alltrans retinoic acid of high specific activity (up to \(\sim 51\) \(\mathrm{Ci} / \mathrm{mmol}\) corresponding to \(85 \%\) of theoretical) is converted photolytically within a fraction of a second to a mixture of retinoic acid stereoisomers. One of
High-specific-activity D-[3-3H]pantothenic acid (5 Ci/mmol) was prepared from commercially available beta-[3-3H]alanine employing Escherichia coli strain DV1 (panD2 pan F1). This strain is defective in beta-alanine synthesis and pantothenate uptake, and under appropriate growth conditions converted
## Abstract Lithium borotritide reduction of α‐ionylidene‐acetaldehyde (5) followed by manganese dioxide oxidation provided the tritiated aldehyde (9) which retainad over 95% of the label. On treatment with the ylide derived from ethyl 4‐chloro‐3‐methylcrotonate, ethyl α‐retinoate‐11‐^3^H (14) was