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Volumn 16, Issue 3, 2010, Pages 871-877

Synthesis and application of modular phosphine-phosphoramidite ligands in asymmetric hydroformylation: Structure-selectivity relationship

Author keywords

Asymmetric catalysis; Enantioselectivit; Hydroformylation; Phosphine phosphoramidite ligands; Rhodium

Indexed keywords

2-NAPHTHOLS; ASYMMETRIC CATALYSIS; ASYMMETRIC HYDROFORMYLATION; BINAPHTHYL; LIGAND STRUCTURE; PHOSPHORAMIDITE LIGANDS; STERIC FACTOR; STRUCTURE-SELECTIVITY RELATIONSHIP; STYRENE DERIVATIVES; SYSTEMATIC VARIATION; VINYL ACETATES;

EID: 75249103032     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200902238     Document Type: Article
Times cited : (92)

References (45)
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    • This theoretical model does not take account of the chelation of the olefin functionality with the Rh center, which can also influence the enantioface selection during or prior to the insertion step somewhat. Meanwhile, we cannot rule out the possibility that both the steps of Rh-alkyl and Rh-acyl formation are reversible. In such a situation, the enantioselectivity will be affected in the final product-forming Rh-acyl hydorgenolysis step
    • This theoretical model does not take account of the chelation of the olefin functionality with the Rh center, which can also influence the enantioface selection during or prior to the insertion step somewhat. Meanwhile, we cannot rule out the possibility that both the steps of Rh-alkyl and Rh-acyl formation are reversible. In such a situation, the enantioselectivity will be affected in the final product-forming Rh-acyl hydorgenolysis step.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.