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Volumn 7, Issue 2, 2001, Pages 456-464

Preparation and reactions of stannylated amino acids

Author keywords

Amino acids; Cross coupling; Hydrostannation; Molybdenum; Rearrangement

Indexed keywords

ALLYL COMPOUND; AMINO ACID; CHELATE; ESTER; GLYCINE; PROPARGYLIC GLYCINE ESTER; TIN; UNCLASSIFIED DRUG; VINYL DERIVATIVE; VINYLSTANNANE;

EID: 0035910534     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (56)

References (97)
  • 9
    • 0000018350 scopus 로고
    • U. Kazmaier, Angew. Chem. 1994, 106, 1046-1047; Angew. Chem. Int. Ed. Engl. 1994, 33, 998-999.
    • (1994) Angew. Chem. , vol.106 , pp. 1046-1047
    • Kazmaier, U.1
  • 10
    • 33748826144 scopus 로고
    • U. Kazmaier, Angew. Chem. 1994, 106, 1046-1047; Angew. Chem. Int. Ed. Engl. 1994, 33, 998-999.
    • (1994) Angew. Chem. Int. Ed. Engl. , vol.33 , pp. 998-999
  • 11
  • 15
    • 0001394530 scopus 로고
    • a) U. Kazmaier, A. Krebs, Angew. Chem. 1995, 107, 2213-2214; Angew. Chem. Int. Ed. Engl. 1995, 34, 2012-2013;
    • (1995) Angew. Chem. , vol.107 , pp. 2213-2214
    • Kazmaier, U.1    Krebs, A.2
  • 16
    • 33748845721 scopus 로고
    • a) U. Kazmaier, A. Krebs, Angew. Chem. 1995, 107, 2213-2214; Angew. Chem. Int. Ed. Engl. 1995, 34, 2012-2013;
    • (1995) Angew. Chem. Int. Ed. Engl. , vol.34 , pp. 2012-2013
  • 18
    • 0000479923 scopus 로고    scopus 로고
    • U. Kazmaier, F. L. Zumpe, Angew. Chem. 1999, 111, 1572-1574; Angew. Chem. Int. Ed. 1999, 38, 1468-1470.
    • (1999) Angew. Chem. , vol.111 , pp. 1572-1574
    • Kazmaier, U.1    Zumpe, F.L.2
  • 19
    • 0033577898 scopus 로고    scopus 로고
    • U. Kazmaier, F. L. Zumpe, Angew. Chem. 1999, 111, 1572-1574; Angew. Chem. Int. Ed. 1999, 38, 1468-1470.
    • (1999) Angew. Chem. Int. Ed. , vol.38 , pp. 1468-1470
  • 29
    • 33747552079 scopus 로고
    • b) H. M. R. Hoffmann, A. R. Otte, A. Wilde, Angew. Chem. 1992, 104, 224-225; Angew. Chem. Int. Ed. Engl. 1992, 31, 234-235;
    • (1992) Angew. Chem. Int. Ed. Engl. , vol.31 , pp. 234-235
  • 31
    • 33748977875 scopus 로고
    • c) A. R. Otte, A. Wilde, H. M. R. Hoffmann, Angew. Chem. 1994, 106, 1352-1354; Angew. Chem. Int. Ed. Engl. 1994, 33, 1280-1282;
    • (1994) Angew. Chem. Int. Ed. Engl. , vol.33 , pp. 1280-1282
  • 33
    • 0003172598 scopus 로고
    • d) H. M. R. Hoffmann, A. R. Otte, A. Wilde, S. Menzer, D. J. Williams, Angew. Chem. 1995, 107, 73-76; Angew. Chem. Int. Ed. Engl. 1995, 34, 100-103.
    • (1995) Angew. Chem. Int. Ed. Engl. , vol.34 , pp. 100-103
  • 34
  • 35
    • 0034681564 scopus 로고    scopus 로고
    • U. Kazmaier, F. L. Zumpe, Angew. Chem. 2000, 112, 805-807; Angew. Chem. Int. Ed. 2000, 39, 802-804.
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 802-804
  • 55
    • 0000103227 scopus 로고
    • J. K. Stille, Angew. Chem. 1986, 98, 504-519; Angew. Chem. Int. Ed. Engl. 1986, 25, 508-523.
    • (1986) Angew. Chem. , vol.98 , pp. 504-519
    • Stille, J.K.1
  • 56
    • 84985570392 scopus 로고
    • J. K. Stille, Angew. Chem. 1986, 98, 504-519; Angew. Chem. Int. Ed. Engl. 1986, 25, 508-523.
    • (1986) Angew. Chem. Int. Ed. Engl. , vol.25 , pp. 508-523
  • 65
    • 85007636223 scopus 로고    scopus 로고
    • note
    • The product ratio was determined by NMR spectroscopy.
  • 71
    • 0000873581 scopus 로고
    • B. Neises, W. Steglich, Angew. Chem. 1978, 90, 556-557; Angew. Chem. Int. Ed. Engl. 1978, 17, 522-523.
    • (1978) Angew. Chem. , vol.90 , pp. 556-557
    • Neises, B.1    Steglich, W.2
  • 72
    • 84985520823 scopus 로고
    • B. Neises, W. Steglich, Angew. Chem. 1978, 90, 556-557; Angew. Chem. Int. Ed. Engl. 1978, 17, 522-523.
    • (1978) Angew. Chem. Int. Ed. Engl. , vol.17 , pp. 522-523
  • 73
    • 85007643660 scopus 로고    scopus 로고
    • note
    • Decompositions such as protodestannylations are commonly observed during chromatography.
  • 80
    • 85007643685 scopus 로고    scopus 로고
    • note
    • 1H NMR spectroscopy.
  • 82
    • 0002564128 scopus 로고
    • For reviews on Claisen and related sigmatropic rearrangements see: a) P. A. Bartlett, Tetrahedron 1980, 36, 3-72;
    • (1980) Tetrahedron , vol.36 , pp. 3-72
    • Bartlett, P.A.1
  • 85
    • 0000217402 scopus 로고
    • (Eds.: B. M. Trost, I. Fleming), Pergamon, New York
    • d) P. Wipf in Comprehensive Organic Synthesis Vol. 5 (Eds.: B. M. Trost, I. Fleming), Pergamon, New York, 1991, 827-873;
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 827-873
    • Wipf, P.1
  • 86
    • 0008823472 scopus 로고
    • (Eds.: J. Mulzer, H.-J. Altenbach, M. Braun, K. Krohn, H.-U. Reissig), VCH, Weinheim
    • e) H.-J. Altenbach in Organic Synthesis Highlights (Eds.: J. Mulzer, H.-J. Altenbach, M. Braun, K. Krohn, H.-U. Reissig), VCH, Weinheim, 1991, pp. 111-128;
    • (1991) Organic Synthesis Highlights , pp. 111-128
    • Altenbach, H.-J.1
  • 88
    • 0001377606 scopus 로고
    • (Eds.: G. Helmchen, R. W. Hoffmann, J. Mulzer, E. Schaumann), Thieme, Stuttgart
    • g) H. Frauenrath in Houben-Weyl E21d (Eds.: G. Helmchen, R. W. Hoffmann, J. Mulzer, E. Schaumann), Thieme, Stuttgart, 1995, pp. 3301-3756.
    • (1995) Houben-Weyl E21d , pp. 3301-3756
    • Frauenrath, H.1
  • 89
    • 85007630204 scopus 로고    scopus 로고
    • note
    • The corresponding acetate 9a can be used as well, but the yields obtained with carbonates are generally better (see refs. [9-11]).
  • 93
    • 85007643619 scopus 로고    scopus 로고
    • note
    • The reaction of Sa was complete after 30 s.
  • 95
    • 0343093825 scopus 로고
    • N. A. Bumagin, I. G. Bumagina, A. N. Kashin, I. P. Beletskaya, Zh. Org. Khim. 1982, 18, 1131-1137; J. Org. Chem. USSR 1982, 18, 977-981.
    • (1982) J. Org. Chem. USSR , vol.18 , pp. 977-981


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.