메뉴 건너뛰기




Volumn 67, Issue 24, 2011, Pages 4358-4363

Synthesis of new serine-based phosphinooxazoline ligands and iridium complexes for asymmetric hydrogenations

Author keywords

Asymmetric catalysis; Hydrogenation; Iridium; P,N Ligands

Indexed keywords

ACETOPHENONE N PHENYLIMINE; ALKENE DERIVATIVE; IMINE; IRIDIUM COMPLEX; LEUCINE; OXAZOLINE DERIVATIVE; PHOSPHINOOXAZOLINE; SERINE; UNCLASSIFIED DRUG;

EID: 79957470406     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2011.02.021     Document Type: Article
Times cited : (17)

References (50)
  • 1
    • 79957486501 scopus 로고    scopus 로고
    • Reviews
    • Reviews:
  • 6
    • 79957502121 scopus 로고    scopus 로고
    • Selected, recent examples
    • Selected, recent examples:
  • 29
    • 79957504471 scopus 로고    scopus 로고
    • Ligand 10 and the corresponding TBDMS ether were reported by Stoltz and coworkers. In a palladium-catalyzed enantioselective decarboxylative protonation the TBDMS derivative was found to be inferior to the tert-butyl phosphinooxazoline ligand
    • Ligand 10 and the corresponding TBDMS ether were reported by Stoltz and coworkers. In a palladium-catalyzed enantioselective decarboxylative protonation the TBDMS derivative was found to be inferior to the tert-butyl phosphinooxazoline ligand:
  • 33
    • 79957452086 scopus 로고    scopus 로고
    • Stohler, R. Ph.D. Thesis, University of Basel, 2006
    • Stohler, R. Ph.D. Thesis, University of Basel, 2006.
  • 34
    • 79957456517 scopus 로고    scopus 로고
    • For reaction conditions and additional asymmetric hydrogenation experiments see the Supplementary data
    • For reaction conditions and additional asymmetric hydrogenation experiments see the Supplementary data.
  • 35
    • 79957532524 scopus 로고    scopus 로고
    • int=0.00), 29,618 used in all calculations. The final wR was 0.0500 (all data). For a selection of bond lengths and angles see the supplementary data. Crystallographic data (excluding structure factors) for 31 have been deposited with the Cambridge Crystallographic Data Center as supplementary publication no. CCDC-805973. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK (fax: +44 1223 336033 or e-mail
    • int=0.00), 29,618 used in all calculations. The final wR was 0.0500 (all data). For a selection of bond lengths and angles see the supplementary data. Crystallographic data (excluding structure factors) for 31 have been deposited with the Cambridge Crystallographic Data Center as supplementary publication no. CCDC-805973. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK (fax: +44 1223 336033 or e-mail: deposit@ccdc.cam.ac.uk ).
  • 41
    • 79957517430 scopus 로고    scopus 로고
    • For details of the X-ray crystallograhic investigations see the Supplementary data
    • For details of the X-ray crystallograhic investigations see the Supplementary data.
  • 46
    • 79957469547 scopus 로고    scopus 로고
    • 13C) ppm, respectively, were used to calibrate the spectra
    • 13C) ppm, respectively, were used to calibrate the spectra.
  • 50
    • 79957534055 scopus 로고    scopus 로고
    • R 14.2 (product) and 16.1 (substrate) min
    • R 14.2 (product) and 16.1 (substrate) min.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.