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Volumn 6, Issue 1, 2000, Pages 139-150

Probing the mechanisms of enantioselective hydrogenation of simple olefins with chiral rhodium catalysts in the presence of anions

Author keywords

Alkenes; Asymmetric catalysis; Halides; Rhodium; Sulfonates

Indexed keywords

2 PHENYL 1 BUTENE; ALKENE DERIVATIVE; ANION; ARYLBUTYRIC ACID DERIVATIVE; HALIDE; RHODIUM; SULFONIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0033967480     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1521-3765(20000103)6:1<139::AID-CHEM139>3.0.CO;2-U     Document Type: Article
Times cited : (37)

References (103)
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    • note
    • By unsaturate route, we mean binding of the olefin prior to addition of molecular hydrogen; the dihydride route refers to addition of molecular hydrogen to form a dihyride species before olefin binding. See reference [10c].
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    • 1/2, probably due to other competing equilibria as shown in Scheme 3 which render this system more complicated.
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    • Rh,P = 190 Hz).
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    • Note that Marks and co-workers also confirmed the validity of the optical rotation data of Lardicci et al. through independent synthesis (reference [7a])
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.