추천 제품
형태
solid
Quality Level
광학 활성
[α]22/D +339°, c = 0.5% in chloroform
반응 적합성
core: ruthenium
reagent type: catalyst
mp
260-268 °C
저장 온도
2-8°C
SMILES string
Cc1ccc(cc1)S(=O)(=O)N2[C@H]([C@@H]([N@@H](CCCc3ccccc3)[Ru]2Cl)c4ccccc4)c5ccccc5
InChI
1S/C30H31N2O2S.ClH.Ru/c1-24-19-21-28(22-20-24)35(33,34)32-30(27-17-9-4-10-18-27)29(26-15-7-3-8-16-26)31-23-11-14-25-12-5-2-6-13-25;;/h2-10,12-13,15-22,29-31H,11,14,23H2,1H3;1H;/q-1;;+2/p-1/t29-,30-;;/m0../s1
InChI key
MDABGVLQRDDWLY-ARDORAJISA-M
애플리케이션
[(S,S)-Teth-TsDpen RuCl] is a catalyst for the asymmetric hydrogenation of ketones. It can be used as a catalyst:
- In the reduction of a ketone intermediate for the synthesis of esketamine.
- In asymmetric hydrogenation of acetylenic ketones.
- For the preparation of (3S,6S)-1,8-diphenylocta-1,7-diyne-3,6-diol starting from 1,8-diphenylocta-1,7-diyne-3,6-dione.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
이미 열람한 고객
Asymmetric transfer hydrogenation of functionalized acetylenic ketones
The Journal of Organic Chemistry, 78(17), 8594-8605 (2013)
Journal of the American Chemical Society, 127(20), 7318-7319 (2005-05-19)
Ruthenium dimer 6 (readily available in two steps from TsDPEN) is converted directly to monomeric asymmetric transfer hydrogenation catalyst 3 in situ under the conditions employed for ketone reduction. Catalyst 3 is a significantly more active catalyst for this application
Iron cyclopentadienone complexes derived from C 2-symmetric bis-propargylic alcohols; preparation and applications to catalysis
Dalton Transactions, 45(9), 3992-4005 (2016)
Enantioselective Syntheses of (S)-Ketamine and (S)-Norketamine
Organic Letters, 21(16), 6575-6578 (2019)
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