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Volumn 43, Issue 26, 2004, Pages 3471-3473

A staudinger approach towards binol-derived MAP-type bidentate P,N ligands

Author keywords

Azides; Biaryl compounds; Nucleophilic aromatic substitution; P ligands

Indexed keywords

NITROGEN COMPOUNDS; PHOSPHATES; REACTION KINETICS;

EID: 4544291112     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200454146     Document Type: Article
Times cited : (35)

References (38)
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    • R. Noyori in Asymmetric Catalysis in Organic Synthesis, Wiley, New York, 1994; Catalytic Asymmetric Synthesis (Ed.: I. Ojima), Wiley-VCH, Weinheim, 2000; Comprehensive Asymmetric Catalysis (Eds.: E. N. Jacobson, A. Pfaltz, H. Yamamoto), Springer, Heidelberg, 1999; M. McCarthy, P. J. Guiry, Tetrahedron 2001, 57, 3809-3844.
    • (2000) Catalytic Asymmetric Synthesis
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    • (1999) Comprehensive Asymmetric Catalysis
  • 4
    • 0035971715 scopus 로고    scopus 로고
    • R. Noyori in Asymmetric Catalysis in Organic Synthesis, Wiley, New York, 1994; Catalytic Asymmetric Synthesis (Ed.: I. Ojima), Wiley-VCH, Weinheim, 2000; Comprehensive Asymmetric Catalysis (Eds.: E. N. Jacobson, A. Pfaltz, H. Yamamoto), Springer, Heidelberg, 1999; M. McCarthy, P. J. Guiry, Tetrahedron 2001, 57, 3809-3844.
    • (2001) Tetrahedron , vol.57 , pp. 3809-3844
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    • P. Kočovský, Š. Vyskočil, M. Smrčina, Chem. Rev. 2003, 103, 3213-3245; for a comprehensive review on N,P ligands in general, see: P. J. Guiry, C. P. Saunders, Adv. Synth. Catal. 2004, 346, 497-537.
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    • Kočovský, P.1    Vyskočil, Š.2    Smrčina, M.3
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    • P. Kočovský, Š. Vyskočil, M. Smrčina, Chem. Rev. 2003, 103, 3213-3245; for a comprehensive review on N,P ligands in general, see: P. J. Guiry, C. P. Saunders, Adv. Synth. Catal. 2004, 346, 497-537.
    • (2004) Adv. Synth. Catal. , vol.346 , pp. 497-537
    • Guiry, P.J.1    Saunders, C.P.2
  • 11
    • 0033524686 scopus 로고    scopus 로고
    • A formal synthesis of MAP-type ligands from (R)-binol can be envisioned as (R)-nobin has been prepared from (R)-binol in 6 steps (61% overall yield); see: R. A. Singer, S. L. Buchwald, Tetrahedron Lett. 1999, 40, 1095-1098.
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    • For the introduction of phosphane and phosphane oxide groups, see: I. P. Beletskaya, M. A. Kazankova, Russ. J. Org. Chem. 2002, 38, 1391-1430; for the introduction of aryl groups, see: T. Hayashi, J. W. Han, A. Takeda, J. Tang, K. Nohmi, K. Mukaide, H. Tsuji, Y. Uozumi, Adv. Synth. Catal. 2001, 343, 279-283.
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    • a) O. David, W. J. N. Meester, H. Bieräugel, H. E. Schoemaker, H. Hiemstra, J. H. van Maarseveen, Angew. Chem. 2003, 115, 4509-4511; Angew. Chem. Int. Ed. 2003, 42, 4373-4375;
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    • for the original work on Staudinger ligations, see: b) E. Saxon, C. R. Bertozzi, Science 2000, 287, 2007-2010;
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    • CCDC 239743 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge via www.ccdc.cam.ac.uk/conts/ retrieving.html (or from the Cambridge Crystallographic Data Centre, 12, Union Road, Cambridge CB2 1EZ, UK; fax: (+44) 1223-336-033; or deposit@ ccdc.cam.ac.uk).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.