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Volumn , Issue 18, 2000, Pages 3235-3245

Cyclopropyl building blocks for organic synthesis, 58(+): A new short access to amino acids incorporating an aminocyclopropyl moiety from N,N-dibenzylcarboxamides

Author keywords

Amino acids; Carboxylic acids; Cyclopropanations; Cyclopropylamines; Titanium

Indexed keywords

AMINO ACID DERIVATIVE; N,N DIBENZYLCARBOXAMIDE DERIVATIVE; TITANIUM; UNCLASSIFIED DRUG;

EID: 0033808090     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/1099-0690(200009)2000:18<3235::aid-ejoc3235>3.0.co;2-7     Document Type: Article
Times cited : (34)

References (59)
  • 9
    • 0028817304 scopus 로고
    • W. Boland, J. Hopke, J. Donath, J. Nüske, F. Bublitz, Angew. Chem. 1995, 107, 1715-1717; Angew. Chem. Int. Ed. Engl. 1995, 34, 1600-1602.
    • (1995) Angew. Chem. Int. Ed. Engl. , vol.34 , pp. 1600-1602
  • 15
    • 33748630852 scopus 로고    scopus 로고
    • [5a] V. Chaplinski, A. de Meijere, Angew. Chem. 1996, 108, 491-492; Angew. Chem. Int. Ed. Engl. 1996, 35, 413-414.
    • (1996) Angew. Chem. Int. Ed. Engl. , vol.35 , pp. 413-414
  • 28
    • 0027962461 scopus 로고
    • The other main route consists of a double alkylation of malonates or glycine equivalents with 1,2-dielectrophiles, see e.g.: [8a] C. Fliche, J. Braun, F. Le Groffic, Synth. Commun. 1994, 24, 2873-2876.
    • (1994) Synth. Commun. , vol.24 , pp. 2873-2876
    • Fliche, C.1    Braun, J.2    Le Groffic, F.3
  • 38
    • 84982061374 scopus 로고
    • Benzyloxyacetic acid (12) is also commercially available, but in this work it was prepared as shown in Scheme 3 according to a published procedure with the sole modification that the sodium salt was used instead of the free acid, which saved one equivalent of sodium benzylate: H. O. L. Fischer, B. Gohlke, Helv. Chim. Acta 1933, 1130-1142.
    • (1933) Helv. Chim. Acta , pp. 1130-1142
    • Fischer, H.O.L.1    Gohlke, B.2
  • 39
    • 0343362709 scopus 로고    scopus 로고
    • Dissertation, Universität Göttingen
    • [12a] M. Kordes, Dissertation, Universität Göttingen, 1999.
    • (1999)
    • Kordes, M.1
  • 40
    • 0342927506 scopus 로고    scopus 로고
    • Dissertation, Universität Göttingen, in progress. - This subject is also part of a forthcoming publication
    • H. Winsel, Dissertation, Universität Göttingen, 2000, in progress. - This subject is also part of a forthcoming publication.
    • (2000)
    • Winsel, H.1
  • 41
    • 0342927504 scopus 로고
    • Eds.: D. Enders, R. Noyori, B. M. Trost, Thieme, Stuttgart
    • P. J. Kocienski, Protecting Groups (Eds.: D. Enders, R. Noyori, B. M. Trost), Thieme, Stuttgart, 1994, p. 221.
    • (1994) Protecting Groups , pp. 221
    • Kocienski, P.J.1
  • 48
    • 0028898969 scopus 로고
    • Slightly different assignments have been reported
    • [18a] K. Burgess, W. Li, Tetrahedron Lett. 1995, 36, 2725-2728. - Slightly different assignments have been reported:
    • (1995) Tetrahedron Lett. , vol.36 , pp. 2725-2728
    • Burgess, K.1    Li, W.2
  • 51
    • 4243811754 scopus 로고
    • DIAD has been reported to give fewer side-products than DEAD in this Mitsunobu-type reaction: B. T. Golding, C. Howes, J. Chem. Res. (S) 1984, 1; J. Chem. Res. (M) 1984, 0101-0110.
    • (1984) J. Chem. Res. (S) , vol.1 , pp. 0101-0110
    • Golding, B.T.1    Howes, C.2
  • 52
    • 4243689258 scopus 로고
    • DIAD has been reported to give fewer side-products than DEAD in this Mitsunobu-type reaction: B. T. Golding, C. Howes, J. Chem. Res. (S) 1984, 1; J. Chem. Res. (M) 1984, 0101-0110.
    • (1984) J. Chem. Res. (M) , pp. 0101-0110


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.