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| (1R,2R)-(-)-[1,2-CYCLOHEXANEDIAMINO-N N'-BIS(3,5-DI-T-BUTYLSALICYLIDENE)]CHROMIUM (III) CHLORIDE Basic information | Reactions |
Product Name: | (1R,2R)-(-)-[1,2-CYCLOHEXANEDIAMINO-N N'-BIS(3,5-DI-T-BUTYLSALICYLIDENE)]CHROMIUM (III) CHLORIDE | Synonyms: | (1R,2R)-(-)-[1,2-CYCLOHEXANEDIAMINO-N N'-BIS(3,5-DI-T-BUTYLSALICYLIDENE)]CHROMIUM (III) CHLORIDE;(1R,2R)-(-)-〔1,2-Cyclohexanediamino-N,N-bis(3,5-di-t-butylsalicylidene)〕chromium(Ⅲ) Chloride;(1R,2R)-(-)-[1,2-Cyclohexanediamino-N,N'-bis(3,5-di-tert-butylsalicylidene)]chromium(III)chloride;(r,r)-n,n'-bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminochromium(iii) chloride;(r,r)-n,n'-bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexan;Chromium,chloro[[2,2'-[(1R,2R)-1,2-cyclohexanediylbis[(nitrilo-kN)methylidyne]]bis[4,6-bis(1,1-dimethylethyl)phenolato-kO]](2-)]-, (SP-5-13)-;(R,R)Jacbosen;RR,R)-N,N'-bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminochromium(III)chloride | CAS: | 164931-83-3 | MF: | C36H52ClCrN2O2 | MW: | 632.27 | EINECS: | 605-379-1 | Product Categories: | Asymmetric Synthesis;Chiral Catalysts, Ligands, and Reagents;CycloadditionChiral Catalysts, Ligands, and Reagents;Privileged Ligands and Complexes;SALENs | Mol File: | 164931-83-3.mol | |
| (1R,2R)-(-)-[1,2-CYCLOHEXANEDIAMINO-N N'-BIS(3,5-DI-T-BUTYLSALICYLIDENE)]CHROMIUM (III) CHLORIDE Chemical Properties |
Melting point | >350 °C(lit.) | form | Powder | color | brown |
Hazard Codes | Xn | Risk Statements | 20/21/22 | Safety Statements | 26-36 | WGK Germany | 3 |
| (1R,2R)-(-)-[1,2-CYCLOHEXANEDIAMINO-N N'-BIS(3,5-DI-T-BUTYLSALICYLIDENE)]CHROMIUM (III) CHLORIDE Usage And Synthesis |
Reactions |
- Catalyst for the asymmetric ring-opening of meso-epoxides and for the kinetic resolution of terminal epoxides.
- Precatalyst for asymmetric Diels-Alder and hetero Diels-Alder reactions.
- Catalyst for copolymerization of CO2 and epoxides.
- Catalyst for enantioselective alkylation of tributyltin enolates.
- Enantioselective addition of Me2Zn to aldehydes.
- Enantioselective intramolecular addition of tertiary enamides to ketones.
- Asymmetric iodocyclization.
- Catalytic intermolecular linear allylic C-H animation.
| Uses | Catalyst used for:
- Asymmetric anti-Mannich reactions
- Coupling reactions
- Ring-opening and Diels-Alder reactions
- Allylic C-H oxidation of terminal alkenes
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| (1R,2R)-(-)-[1,2-CYCLOHEXANEDIAMINO-N N'-BIS(3,5-DI-T-BUTYLSALICYLIDENE)]CHROMIUM (III) CHLORIDE Preparation Products And Raw materials |
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