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Volumn 73, Issue 14, 2008, Pages 5410-5415

Formation of spirocyclic compounds from heck cyclizations invoking cyclic enamides

Author keywords

[No Author keywords available]

Indexed keywords

AMIDES; AMINES; ARSENIC COMPOUNDS; CHEMICAL REACTIONS; DIFFERENCE EQUATIONS; MATHEMATICAL TRANSFORMATIONS; PALLADIUM;

EID: 48249127916     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo800650e     Document Type: Article
Times cited : (26)

References (67)
  • 1
    • 0032335204 scopus 로고    scopus 로고
    • For reviews, see: a
    • For reviews, see: (a) Crisp, G. T. Chem. Soc. Rev. 1998, 27, 427-436.
    • (1998) Chem. Soc. Rev , vol.27 , pp. 427-436
    • Crisp, G.T.1
  • 4
    • 0012857368 scopus 로고    scopus 로고
    • (d) Link, J. T. Org. React. 2002, 60, 157-534.
    • (2002) Org. React , vol.60 , pp. 157-534
    • Link, J.T.1
  • 11
    • 0037288964 scopus 로고    scopus 로고
    • For reviews, see: a
    • For reviews, see: (a) Catellani, M. Synlett 2003, 298-313.
    • (2003) Synlett , pp. 298-313
    • Catellani, M.1
  • 14
  • 38
    • 0034681467 scopus 로고    scopus 로고
    • For some recent examples of reductive Heck cyclizations, see: a
    • For some recent examples of reductive Heck cyclizations, see: (a) Sole, D.; Bonjoch, J.; Garcia-Rubio, S.; Peidro, E.; Bosch, J. Chem. Eur. J. 2000, 6, 655-665.
    • (2000) Chem. Eur. J , vol.6 , pp. 655-665
    • Sole, D.1    Bonjoch, J.2    Garcia-Rubio, S.3    Peidro, E.4    Bosch, J.5
  • 44
    • 0000920196 scopus 로고    scopus 로고
    • For some examples of bimolecular reductive Heck coupling reactions, see: a
    • For some examples of bimolecular reductive Heck coupling reactions, see: (a) Namyslo, J. C.; Kaufmann, D. E. Chem. Ber./Recueil 1997, 130, 1327-1331.
    • (1997) Chem. Ber./Recueil , vol.130 , pp. 1327-1331
    • Namyslo, J.C.1    Kaufmann, D.E.2
  • 50
    • 33644950838 scopus 로고    scopus 로고
    • (b) Dake, G. Tetrahedron 2006, 62, 3467-3492.
    • (2006) Tetrahedron , vol.62 , pp. 3467-3492
    • Dake, G.1
  • 51
    • 0032488588 scopus 로고    scopus 로고
    • For some recent papers describing the synthesis of 7-azaspiro[4.5]decane derivatives, see: (a) Yang, L.; Morriello, G.; Prendergast, K.; Cheng, K.; Jacks, T.; Chan, W. W. S.; Schleim, K. D.; Smith, R. G.; Patchett, A. A. Bioorg. Med. Chem. Lett. 1998, 8, 107-112.
    • For some recent papers describing the synthesis of 7-azaspiro[4.5]decane derivatives, see: (a) Yang, L.; Morriello, G.; Prendergast, K.; Cheng, K.; Jacks, T.; Chan, W. W. S.; Schleim, K. D.; Smith, R. G.; Patchett, A. A. Bioorg. Med. Chem. Lett. 1998, 8, 107-112.
  • 54
    • 0000284493 scopus 로고    scopus 로고
    • Compound 8b: (a) Bard, R. R.; Bunnett, J. F.; Traber, R. P. J. Org. Chem. 1979, 44, 4918-4924.
    • Compound 8b: (a) Bard, R. R.; Bunnett, J. F.; Traber, R. P. J. Org. Chem. 1979, 44, 4918-4924.
  • 56
    • 0033533792 scopus 로고    scopus 로고
    • Compound 8c: Vu, C. B.; Corpuz, E. G.; Merry, T. J.; Pradeepan, S. G.; Bartlett, C.; Bohacek, R. S.; Botfield, M. C.; Eyermann, C. J.; Lynch, B. A.; MacNeil; I. A; Ram, M. K.; van Schravendijk, M. R.; Violette, S.; Sawyer, T. K. J. Med. Chem. 1999, 42, 4088-4098.
    • Compound 8c: Vu, C. B.; Corpuz, E. G.; Merry, T. J.; Pradeepan, S. G.; Bartlett, C.; Bohacek, R. S.; Botfield, M. C.; Eyermann, C. J.; Lynch, B. A.; MacNeil; I. A; Ram, M. K.; van Schravendijk, M. R.; Violette, S.; Sawyer, T. K. J. Med. Chem. 1999, 42, 4088-4098.
  • 57
    • 0035852126 scopus 로고    scopus 로고
    • Compound 8d: (a) Kuwabe, S.-i.; Torraca, K. E.; Buchwald, S. L. J. Am. Chem. Soc. 2001, 123, 12202-12206.
    • Compound 8d: (a) Kuwabe, S.-i.; Torraca, K. E.; Buchwald, S. L. J. Am. Chem. Soc. 2001, 123, 12202-12206.
  • 59
    • 0028846892 scopus 로고    scopus 로고
    • Compound 8e, 8f: Orito, K.; Hatakeyama, T.; Takeo, M.; Suginome, H. Synthesis 1995, 1273-1277.
    • Compound 8e, 8f: Orito, K.; Hatakeyama, T.; Takeo, M.; Suginome, H. Synthesis 1995, 1273-1277.
  • 65
    • 38749127622 scopus 로고    scopus 로고
    • and references therein. For an example, where iridium functions as a hydride shuttle, see
    • For an example, where iridium functions as a hydride shuttle, see: Yamaguchi, R.; Kawagoe, S.; Asai, C.; Fujita, K.-i. Org. Lett. 2008, 10, 181-184, and references therein.
    • (2008) Org. Lett , vol.10 , pp. 181-184
    • Yamaguchi, R.1    Kawagoe, S.2    Asai, C.3    Fujita, K.-I.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.