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Volumn 49, Issue 36, 2010, Pages 6421-6424

Electron-donating and rigid p-stereogenic bisphospholane ligands for highly enantioselective rhodium-catalyzed asymmetric hydrogenations

Author keywords

Asymmetric synthesis; Hydrogenation; Ligand design; P stereogenic ligands; Rhodium

Indexed keywords

ASYMMETRIC HYDROGENATION; ASYMMETRIC SYNTHESIS; ELECTRON-DONATING; ENANTIOSELECTIVE; FUNCTIONALIZED; LIGAND DESIGN; NORBORNADIENE; P-STEREOGENIC LIGANDS; RHODIUM-CATALYZED;

EID: 77956034350     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201002990     Document Type: Article
Times cited : (106)

References (45)
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    • See the Supporting Information for details. A similar strategy to form P-stereogenic phosphorus ligands was also applied in the Esphos (1,1'-(1,2-phenylene)bis[hexahydro-2-phenyl-1Hpyrrolo[1,2-c],3,diazaphosphole]) type of ligands, see
    • See the Supporting Information for details. A similar strategy to form P-stereogenic phosphorus ligands was also applied in the Esphos (1,1'-(1,2-phenylene)bis[hexahydro-2-phenyl-1Hpyrrolo[1,2-c],3,diazaphosphole]) type of ligands, see: S. Breeden, M. Wills, J. Org. Chem. 1999, 64, 9735-9738.
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    • CCDC 776144 (8) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • CCDC 776144 (8) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
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    • These are not optimal reaction condition. To compare with the results of TangPhos, the same reaction conditions were used
    • These are not optimal reaction condition. To compare with the results of TangPhos, the same reaction conditions were used.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.