메뉴 건너뛰기




Volumn 130, Issue 52, 2008, Pages 17638-17639

Copper catalyzed enantioselective intramolecular aminooxygenation of alkenes

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ALCOHOLS; COPPER CATALYZED; COPPER TRIFLATE; DISSOLVING METAL REDUCTION; ENANTIOSELECTIVE; FUNCTIONALIZED; HIGH YIELD; PYRROLIDINES; STOICHIOMETRIC OXIDANT;

EID: 58849098107     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja806585m     Document Type: Short Survey
Times cited : (225)

References (28)
  • 2
    • 0033083525 scopus 로고    scopus 로고
    • Reviews of enantioselective aminohydroxylation processes: a
    • Reviews of enantioselective aminohydroxylation processes: (a) O'Brien, P. Angew. Chem., Int. Ed. 1999, 38, 326.
    • (1999) Angew. Chem., Int. Ed , vol.38 , pp. 326
    • O'Brien, P.1
  • 13
    • 0037034854 scopus 로고    scopus 로고
    • For other intramolecular aminooxygenation reactions, see: a
    • For other intramolecular aminooxygenation reactions, see: (a) Noack, M.; Gottlich, R. Chem. Commun. 2002, 536.
    • (2002) Chem. Commun , pp. 536
    • Noack, M.1    Gottlich, R.2
  • 18
    • 67849110117 scopus 로고    scopus 로고
    • For recent Cu- and Pd-catalyzed intermolecular aminooxygenation reactions, see Supporting Information.
    • (f) For recent Cu- and Pd-catalyzed intermolecular aminooxygenation reactions, see Supporting Information.
  • 21
    • 67849124452 scopus 로고    scopus 로고
    • vanLingen, H. L.; vanDelft, L. F.; Storcken, R. P. M.; Hekking, K. F. W.; Klaasen, A.; Smits, J. J. M.; Ruskowska, P.; Frelek, J.; Rutjes, F. P. J. T. Eur. J. Org. Chem. 2005, n/a, 2975.
    • vanLingen, H. L.; vanDelft, L. F.; Storcken, R. P. M.; Hekking, K. F. W.; Klaasen, A.; Smits, J. J. M.; Ruskowska, P.; Frelek, J.; Rutjes, F. P. J. T. Eur. J. Org. Chem. 2005, n/a, 2975.
  • 22
    • 0030597018 scopus 로고    scopus 로고
    • Desimoni, G.; Faita, G.; Mella, M. Tetrahedron 1996, n/a, 13649.
    • Desimoni, G.; Faita, G.; Mella, M. Tetrahedron 1996, n/a, 13649.
  • 23
    • 67849095525 scopus 로고    scopus 로고
    • N-Tosyl-2-allyl-benzylamine did not provide the corresponding six-membered ring aminooxygenation product.
    • N-Tosyl-2-allyl-benzylamine did not provide the corresponding six-membered ring aminooxygenation product.
  • 24
    • 1442349810 scopus 로고    scopus 로고
    • Kan, T.; Fukuyama, T. Chem. Commun. 2004, n/a, 353.
    • Kan, T.; Fukuyama, T. Chem. Commun. 2004, n/a, 353.
  • 25
    • 67849119713 scopus 로고    scopus 로고
    • A discussion of the C-O bond forming mechanism is provided in the Supporting Information
    • A discussion of the C-O bond forming mechanism is provided in the Supporting Information.
  • 28
    • 67849086967 scopus 로고    scopus 로고
    • Compound 9, an intermediate en route to a chiral ligand, was previously synthesized in a more lengthy sequence from L-glutamic acid: Nagaoka, Y.; Tomioka, K.; Nakagawa, Y.; Kanai, M. Tetrahedron 1998, 54, 10295.
    • Compound 9, an intermediate en route to a chiral ligand, was previously synthesized in a more lengthy sequence from L-glutamic acid: Nagaoka, Y.; Tomioka, K.; Nakagawa, Y.; Kanai, M. Tetrahedron 1998, 54, 10295.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.