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752800

Sigma-Aldrich

[(S,S)-Teth-TsDpen RuCl]

别名:

stereoisomer of Chloro[N-[(1S,2S)-1,2-diphenyl-2-[(R)-[3-(η6-phenyl)propyl]amino-κN]ethyl]-4-methylbenzenesulfonamidato-κN]ruthenium

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About This Item

经验公式（希尔记法）:
C30H31ClN2O2RuS
CAS号:
851051-43-9
分子量:
620.17
MDL编号:
MFCD16294984
UNSPSC代码:
12352103
PubChem化学物质编号:
329766311
NACRES:
NA.22

表单

solid

质量水平

100

旋光性

[α]22/D +339°, c = 0.5% in chloroform

反应适用性

core: ruthenium
reagent type: catalyst

mp

260-268 °C

储存温度

2-8°C

SMILES字符串

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

相关类别

应用

[(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.

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
MKCR9975
MKCS0064
MKCS4034
MKCQ5723
MKCQ4458

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Iron cyclopentadienone complexes derived from C 2-symmetric bis-propargylic alcohols; preparation and applications to catalysis
Hodgkinson R, et al.
Dalton Transactions, 45(9), 3992-4005 (2016)
Asymmetric transfer hydrogenation of functionalized acetylenic ketones
Fang Z and Wills M
The Journal of Organic Chemistry, 78(17), 8594-8605 (2013)
Aidan M Hayes et al.
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
Enantioselective Syntheses of (S)-Ketamine and (S)-Norketamine
Chen C and Lu X
Organic Letters, 21(16), 6575-6578 (2019)

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