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Volumn , Issue 11, 2010, Pages 2157-2175

Synthesis of phosphanyl sulfoximines through phospha-michael reaction of alkenyl sulfoximines and their evaluation as chiral bidentate 1, 5-N, P ligands for palladium in asymmetric allylic alkylation

Author keywords

Alkylation; Asymmetric allylic alkylation; Palladium; Phospha michael reaction; Sulfoximine

Indexed keywords


EID: 77950232128     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200901462     Document Type: Article
Times cited : (24)

References (116)
  • 1
    • 0001017993 scopus 로고
    • For reviews, see:a
    • For reviews, see: a) C. R. Johnson, Acc. Chem. Res. 1973, 6, 341-347;
    • (1973) Acc. Chem. Res. , vol.6 , pp. 341-347
    • Johnson, C.R.1
  • 3
  • 9
    • 77950220569 scopus 로고    scopus 로고
    • For recent examples
    • For recent examples, see:
  • 33
    • 77950192484 scopus 로고    scopus 로고
    • According to ab initio calculations the sulfoximine group has ylide like S, N- and S, O-single bonds as depicted in Figure 1. However, for convenience the sulfoximine group in the other Figures, Schemes, and Tables is depicted with S,O- and S,N-double bonds
    • According to ab initio calculations the sulfoximine group has ylide like S, N- and S, O-single bonds as depicted in Figure 1. However, for convenience the sulfoximine group in the other Figures, Schemes, and Tables is depicted with S,O- and S,N-double bonds.
  • 34
    • 3042826615 scopus 로고    scopus 로고
    • For ab initio calculations of sulfoximinesa
    • For ab initio calculations of sulfoximines, see: a) C. P. R. Hack- enberger, G. Raabe, C. Bolm, Chem. Eur. J. 2004, 10, 2942-2952;
    • (2004) Chem. Eur. J. , vol.10 , pp. 2942-2952
    • Hack-Enberger, C.P.R.1    Raabe, C.2    Bolm, G.3
  • 38
    • 0035844456 scopus 로고    scopus 로고
    • For N-phosphanyl sulfoximinesa
    • For N-phosphanyl sulfoximines, see: a) T. C. Kinahan, H. Tye, Tetrahedron: Asymmetry 2001, 12, 1255-1257;
    • (2001) Tetrahedron: Asymmetry , vol.12 , pp. 1255-1257
    • Kinahan, T.C.1    Tye, H.2
  • 39
    • 77950248291 scopus 로고    scopus 로고
    • See ref. 4j
    • b) See ref. 4j;
  • 45
    • 0042379988 scopus 로고    scopus 로고
    • For P, P ligands a
    • For P, P ligands, see: a) B. M. Trost, M. L. Crawley, Chem. Rev. ' 2003, 103, 2921-2943;
    • (2003) Chem. Rev. , vol.103 , pp. 2921-2943
    • Trost, B.M.1    Crawley, M.L.2
  • 47
    • 77950287280 scopus 로고    scopus 로고
    • See ref. 10d.
    • See ref. 10d.
  • 75
    • 77950194023 scopus 로고    scopus 로고
    • Ph. D. Thesis, RWTH Aachen, Germany
    • V. B. R. Iska, Ph. D. Thesis, RWTH Aachen, Germany, 2008.
    • (2008)
    • Iska, V.B.R.1
  • 78
    • 77950288166 scopus 로고    scopus 로고
    • Ph.D. Thesis, RWTH Aachen, Germany
    • R. Loo, Ph.D. Thesis, RWTH Aachen, Germany, 1999.
    • (1999)
    • Loo, R.1
  • 90
    • 77950295362 scopus 로고    scopus 로고
    • Ph.D. Thesis, RWTH Aachen
    • P. R. Bruns, Ph.D. Thesis, RWTH Aachen, 20033.
    • (2003)
    • Bruns, P.R.1
  • 92
  • 94
    • 33845327885 scopus 로고    scopus 로고
    • For the α-lithiation of N-alkylalkenyl sulfoximines a
    • For the α-lithiation of N-alkylalkenyl sulfoximines, see: a) Lejkowski, H.-J. Gais, P. Banerjee, C. Vermeeren, J. Am. Chem. Soc. 2006, 128, 15378-15379;
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 15378-15379
    • Lejkowski1    Gais, H.-J.2    Banerjee, P.3    Vermeeren, C.4
  • 96
    • 77950250643 scopus 로고    scopus 로고
    • Phosphane-borane ent-20 was prepared from, ent-6 in the same as 20 from 6
    • Phosphane-borane ent-20 was prepared from, ent-6 in the same as 20 from 6.
  • 102
    • 77950266073 scopus 로고    scopus 로고
    • CCDC-662848 (for ent-20), -662849 (for 29) and -757322 (for 25) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data. Centre via
    • CCDC-662848 (for ent-20), -662849 (for 29) and -757322 (for 25) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data. Centre via www.ccdc.ac.uk/ data-request/cif.
  • 114
    • 77950201852 scopus 로고    scopus 로고
    • π2 and the phenyl group are the same or opposite site of the allyl moiety, respectively
    • π2 and the phenyl group are the same or opposite site of the allyl moiety, respectively.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.