메뉴 건너뛰기




Volumn , Issue 16, 2004, Pages 3377-3383

The allenic Pauson-Khand reaction in synthesis

Author keywords

Allenes; Carbonylation; Cycloaddition; Organometallics; Synthetic methods

Indexed keywords

ALLENE DERIVATIVE;

EID: 4544260813     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/ejoc.200400023     Document Type: Short Survey
Times cited : (102)

References (51)
  • 7
    • 0038665161 scopus 로고    scopus 로고
    • For a review on the catalytic Pauson-Khand reaction, see: S. E. Gibson, A. Stevenazzi, Angew. Chem. Int. Ed. 2003, 42, 1800; Angew. Chem. 2003, 115, 1844.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 1800
    • Gibson, S.E.1    Stevenazzi, A.2
  • 8
    • 0038665161 scopus 로고    scopus 로고
    • For a review on the catalytic Pauson-Khand reaction, see: S. E. Gibson, A. Stevenazzi, Angew. Chem. Int. Ed. 2003, 42, 1800; Angew. Chem. 2003, 115, 1844.
    • (2003) Angew. Chem. , vol.115 , pp. 1844
  • 16
    • 0036126987 scopus 로고    scopus 로고
    • For recent reviews on transition metal catalyzed cyclizations of allenes, see: [8a] R. W. Bates, V. Satcharoen, Chem. Soc. Rev. 2002, 31, 12.
    • (2002) Chem. Soc. Rev. , vol.31 , pp. 12
    • Bates, R.W.1    Satcharoen, V.2
  • 17
    • 0000524295 scopus 로고    scopus 로고
    • [8b] A. S. K. Hashmi, Angew. Chem. 2000, 112, 3737; Angew. Chem. Int. Ed. 2000, 39, 3590. 123, 8416.
    • (2000) Angew. Chem. , vol.112 , pp. 3737
    • Hashmi, A.S.K.1
  • 18
    • 0034675566 scopus 로고    scopus 로고
    • [8b] A. S. K. Hashmi, Angew. Chem. 2000, 112, 3737; Angew. Chem. Int. Ed. 2000, 39, 3590. 123, 8416.
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 3590
  • 19
    • 4544304592 scopus 로고    scopus 로고
    • [8b] A. S. K. Hashmi, Angew. Chem. 2000, 112, 3737; Angew. Chem. Int. Ed. 2000, 39, 3590. 123, 8416.
    • Angew. Chem. Int. Ed. , vol.123 , pp. 8416
  • 34
    • 0030726318 scopus 로고    scopus 로고
    • It has been shown that a titanium(II)-mediated allenyne undergoes a formal [2+2+1] cycloaddition affording cyclopentenones with complete transfer of chirality. However, the product possessing the (x-alkylidene functionality was not isolated, since it experiences a subsequent electrophilic addition by a titanium homoenolate equivalent. See: H. Urabe, T. Takeda, D. Hideura, F. Sato, J. Am. Chem. Soc. 1997, 119, 11295.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 11295
    • Urabe, H.1    Takeda, T.2    Hideura, D.3    Sato, F.4
  • 35
    • 0030818489 scopus 로고    scopus 로고
    • For the use of the PK reaction in the preparation of medium-sized rings with an aromatic ring, see: [19a] J. Barluenga, R. Sanz, F. J. Fañanás, Chem. Eur. J. 1997, 3, 1324.
    • (1997) Chem. Eur. J. , vol.3 , pp. 1324
    • Barluenga, J.1    Sanz, R.2    Fañanás, F.J.3
  • 51
    • 0037693723 scopus 로고    scopus 로고
    • P. A. Wender, N. M. Deschamps, G. G. Gamber, Angew. Chem. Int. Ed. 2003, 42, 1853; Angew Chem. 2003, 115, 1897.
    • (2003) Angew Chem. , vol.115 , pp. 1897


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.