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Volumn 10, Issue 1, 2004, Pages 267-278

Chiral Xyliphos Complexes for the Catalytic Imine Hydrogenation Leading to the Metolachlor Herbicide: Isolation of Catalyst-Substrate Adducts

Author keywords

Asymmetric catalysis; Hydrogenation; Iridium; P ligands

Indexed keywords

CATALYSIS; HYDROGENATION; IRIDIUM COMPOUNDS; ISOMERS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; OXIDATION; SINGLE CRYSTALS; STEREOCHEMISTRY; X RAY DIFFRACTION ANALYSIS;

EID: 0346458583     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/chem.200305218     Document Type: Article
Times cited : (90)

References (40)
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    • note
    • 4.
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    • Note that the indicated TOFs are average values over 18 h and that, depending on the purity of the MEA-imine, reaction times of less than 2 h for total conversion have been observed.
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    • note
    • This is the reverse of our initial and unsuccessful strategy of treating the imine with preformed iridium Xyliphos complexes 7-13.
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    • note
    • 2 at 195 K a hydrido species formed, and no free imine 14 was detected in the mother liquor. To date, we have been unable to isolate this compound in pure form.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.