메뉴 건너뛰기




Volumn 46, Issue 3, 2007, Pages 386-388

Erratum: A highly regio- and stereoselective vinylogous Horner-Wadsworth-Emmons route to densely substituted 1,3-butadienes (Angewandte Chemie - International Edition (2006) 46, (386-388) DOI: 10.1002/anie.200604013);A highly regio- and stereoselective vinylogous Horner-Wadsworth-Emmons route to densely substituted 1,3-butadienes

Author keywords

1,3 dienes; Olefination; Regioselectivity; Vinyl phosphonates; Vinylogous reactions

Indexed keywords

ALDEHYDES; BUTANE; CHEMICAL BONDS; PHOSPHORUS COMPOUNDS; SUBSTITUTION REACTIONS; VINYL RESINS;

EID: 33846440086     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200790054     Document Type: Erratum
Times cited : (21)

References (60)
  • 9
    • 0003397099 scopus 로고
    • Ylides and Imines of Phosphorus
    • d) A. W. Johnson, Ylides and Imines of Phosphorus, Wiley, New York, 1993, pp. 307-358.
    • (1993) Wiley, New York , pp. 307-358
    • Johnson, A.W.1
  • 12
    • 0000595175 scopus 로고    scopus 로고
    • For representative examples of vinylogous reactions, see;
    • For representative examples of vinylogous reactions, see; I. Fleming, A. Berbero, D. Walter, Chem. Rev. 1997, 97, 2063-2192
    • (1997) Chem. Rev , vol.97 , pp. 2063-2192
    • Fleming, I.1    Berbero, A.2    Walter, D.3
  • 15
    • 23044486219 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 4682-4698
    • (2005) Chem. Int. Ed , vol.44 , pp. 4682-4698
    • Angew1
  • 17
    • 0035897085 scopus 로고    scopus 로고
    • Mannich reaction
    • S. K. Bur, S. F. Martin, Tetrahedron 2001, 57, 3221-3242 (Mannich reaction);
    • (2001) Tetrahedron , vol.57 , pp. 3221-3242
    • Bur, S.K.1    Martin, S.F.2
  • 19
    • 0011211458 scopus 로고    scopus 로고
    • Pummerer rearrangement
    • A. Padwa, J. T. Kuethe, J. Org. Chem. 1998, 63, 4256-4268 (Pummerer rearrangement);
    • (1998) J. Org. Chem , vol.63 , pp. 4256-4268
    • Padwa, A.1    Kuethe, J.T.2
  • 21
  • 29
    • 0001432653 scopus 로고    scopus 로고
    • E. Vedejs, J. P. Bershas, P. L. Fuchs, J. Org. Chem. 1973, 38, 3625-3627;
    • c) E. Vedejs, J. P. Bershas, P. L. Fuchs, J. Org. Chem. 1973, 38, 3625-3627;
  • 42
    • 0034677846 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2000, 39, 1125-1128.
    • (2000) Chem. Int. Ed , vol.39 , pp. 1125-1128
    • Angew1
  • 49
    • 0033547964 scopus 로고    scopus 로고
    • The terminology vinylogous HWE reaction was also used for the α condensation of allylic phophonates to aldehydes; see
    • The terminology "vinylogous HWE reaction" was also used for the α condensation of allylic phophonates to aldehydes; see: S. R. Chemler, D. S. Coffey, W. R. Roush, Tetrahedron Lett. 1999, 40, 1269-1272.
    • (1999) Tetrahedron Lett , vol.40 , pp. 1269-1272
    • Chemler, S.R.1    Coffey, D.S.2    Roush, W.R.3
  • 53
    • 33846459850 scopus 로고    scopus 로고
    • The reaction between 8a and benzaldehyde is reported in ref. [9g], but the authors did not observe the formation of 5a or 6a.
    • The reaction between 8a and benzaldehyde is reported in ref. [9g], but the authors did not observe the formation of 5a or 6a.
  • 56
    • 84989585272 scopus 로고
    • For representative examples of approaches based on the Wittig reaction, see: a
    • For representative examples of approaches based on the Wittig reaction, see: a) S. E. Denmark, J. Amburgey, J. Am. Chem. Soc. 1993, 115, 10386-10387;
    • (1993) J. Am. Chem. Soc , vol.115 , pp. 10386-10387
    • Denmark, S.E.1    Amburgey, J.2
  • 59
    • 33645025619 scopus 로고    scopus 로고
    • For the synthesis of trisubstituted conjugated dienes, see:, and references therein
    • For the synthesis of trisubstituted conjugated dienes, see: G. A. Molander, Y. Yokoyama, J. Org. Chem. 2006, 71, 2493-2498, and references therein.
    • (2006) J. Org. Chem , vol.71 , pp. 2493-2498
    • Molander, G.A.1    Yokoyama, Y.2
  • 60
    • 33846429852 scopus 로고    scopus 로고
    • A mechanistic rationale is provided in the Supporting Information
    • A mechanistic rationale is provided in the Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.