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Volumn 48, Issue 28, 2009, Pages 5199-5202

The benzyne aza-claisen reaction

Author keywords

Allylamines; Arynes; Aza Claisen rearrangement; Medium ring compounds

Indexed keywords

ALLYL AMINE; ALLYLAMINES; ARYNES; AZA-CLAISEN REARRANGEMENT; BENZYNE; MEDIUM-RING COMPOUNDS; QUATERNIZATION; SIGMATROPIC SHIFTS;

EID: 70349895352     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200901410     Document Type: Article
Times cited : (110)

References (59)
  • 2
    • 0000209699 scopus 로고    scopus 로고
    • C. D. Hurd, W.W. Jenkins, J. Org. Chem. 1957, 22, 14181423;
    • a) C. D. Hurd, W.W. Jenkins, J. Org. Chem. 1957, 22, 14181423;
  • 5
    • 61349120769 scopus 로고    scopus 로고
    • For recent examples of aza-Claisen. rearrangements, see : a K. L. Bridgwood, C C Tzschucke, M. O'Brien, S. Wittrock, X M. Goodman, X E. Davies, A. W. X Logan, M. R. M. Huttl, S. V Ley, Org. Lett 2008, 10, 4537-4540;
    • For recent examples of aza-Claisen. rearrangements, see : a) K. L. Bridgwood, C C Tzschucke, M. O'Brien, S. Wittrock, X M. Goodman, X E. Davies, A. W. X Logan, M. R. M. Huttl, S. V Ley, Org. Lett 2008, 10, 4537-4540;
  • 9
    • 34250693162 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 3931-3933;
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 3931-3933
  • 25
    • 2142677703 scopus 로고
    • and references therein; For other tertiary amine additions to aryn.es, see: a
    • For other tertiary amine additions to aryn.es, see: a) A.R. Lepley, R. H. Becker, A. G. Giumanini, J. Org. Chem. 1971, 36, 1222-1227, and references therein;
    • (1971) J. Org. Chem , vol.36 , pp. 1222-1227
    • Lepley, A.R.1    Becker, R.H.2    Giumanini, A.G.3
  • 32
    • 33746281785 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 3579-3581.
    • (2006) Angew. Chem. Int. Ed , vol.45 , pp. 3579-3581
  • 33
    • 53849126527 scopus 로고    scopus 로고
    • For recent examples of a-insertion reactions of arynes, see: a S. Krishnan, X T Bagdanoff, D. C Ebner, Y K. Ramtohul, U K. Tambar, B. M. Stoltz, J. Am. Chem Soc. 2008, 130, 1374513754;
    • For recent examples of a-insertion reactions of arynes, see: a) S. Krishnan, X T Bagdanoff, D. C Ebner, Y K. Ramtohul, U K. Tambar, B. M. Stoltz, J. Am. Chem Soc. 2008, 130, 1374513754;
  • 55
    • 0032482103 scopus 로고    scopus 로고
    • Angew. Chem. Int Ed. 1998,37,1140-1143;
    • (1998) Angew. Chem. Int Ed , vol.37 , pp. 1140-1143
  • 57
    • 33748223592 scopus 로고
    • Angew. Chem. Int. Ed. 1995, 34, 1026-1028.
    • (1995) Angew. Chem. Int. Ed , vol.34 , pp. 1026-1028
  • 58
    • 14544304543 scopus 로고    scopus 로고
    • M. Qadir, X Cobb, R W Sheldrake, N. Whittall, A. X P. White, K. K. (M) Hii, R N. Horton, M. B. Hursthouse, J. Org. Chem. 2005, 70, 1552-1557.
    • M. Qadir, X Cobb, R W Sheldrake, N. Whittall, A. X P. White, K. K. (M) Hii, R N. Horton, M. B. Hursthouse, J. Org. Chem. 2005, 70, 1552-1557.
  • 59
    • 70349942636 scopus 로고    scopus 로고
    • V,V-diphenyl-a-naphthylamine was reported as a side product (4%) of benzyne reaction with JV-phenylpyrrole. See Ref. [7b].
    • V,V-diphenyl-a-naphthylamine was reported as a side product (4%) of benzyne reaction with JV-phenylpyrrole. See Ref. [7b].


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.