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Volumn 6, Issue 3, 2011, Pages 899-908

Chiral iridium spiro aminophosphine complexes: Asymmetric hydrogenation of simple ketones, structure, and plausible mechanism

Author keywords

aminophosphines; asymmetric catalysis; hydrogenation; iridium; ketones

Indexed keywords

ACTIVE SPECIES; AMINOPHOSPHINE LIGANDS; AMINOPHOSPHINES; AROMATIC KETONES; ARYL KETONES; ASYMMETRIC CATALYSIS; ASYMMETRIC HYDROGENATION; CHIRAL ALCOHOLS; EFFICIENT CATALYSTS; HIGH ACTIVITY; HIGH ENANTIOSELECTIVITY; HYDROGENATION REACTIONS; IRIDIUM COMPLEX; IRIDIUM DIHYDRIDE; KEY FACTORS; MILD REACTION CONDITIONS; NMR SPECTROSCOPY; PHENYL RINGS; PLAUSIBLE MECHANISMS; TERT-BUTYL GROUP; TURNOVER FREQUENCY; TURNOVER NUMBER;

EID: 79951993225     PISSN: 18614728     EISSN: 1861471X     Source Type: Journal    
DOI: 10.1002/asia.201000716     Document Type: Article
Times cited : (70)

References (82)
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    • For other examples of Ir-catalyzed asymmetric hydrogenations of ketones, see
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    • If the hydrides are trans to the phosphorus atom of the ligand in the iridium complex like in 6 B, larger coupling constants of 150-200 Hz would be expected. For a review, see
    • If the hydrides are trans to the phosphorus atom of the ligand in the iridium complex like in 6 B, larger coupling constants of 150-200 Hz would be expected. For a review, see
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.