메뉴 건너뛰기




Volumn 2, Issue 11, 2009, Pages 1021-1024

The phosphine-catalyzed wittig reaction: A new vista for olefin synthesis?

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; ALKENE; KETONE; PHOSPHINE; PHOSPHINE DERIVATIVE;

EID: 73549094724     PISSN: 18645631     EISSN: 1864564X     Source Type: Journal    
DOI: 10.1002/cssc.200900208     Document Type: Article
Times cited : (37)

References (37)
  • 16
    • 0026418434 scopus 로고
    • B. M. Trost, Science 1991, 254, 1471-1477
    • (1991) Science , vol.254 , pp. 1471-1477
    • Trost, B.M.1
  • 19
    • 85020949506 scopus 로고    scopus 로고
    • 4 or oxalic acid), see, US Patent 5,892,121
    • 4 or oxalic acid), see: D. Hermeling, R. Hugo, H. Siegel, US Patent 5,892,121, 1999
    • (1999)
    • Hermeling, D.1    Hugo, R.2    Siegel, H.3
  • 20
    • 0017373408 scopus 로고
    • Stoichiometric triphenylphosphine can be recycled on an industrial scale, see
    • Stoichiometric triphenylphosphine can be recycled on an industrial scale, see: H. Pommer, Angew. Chem. 1977, 89, 437-443
    • (1977) Angew. Chem. , vol.89 , pp. 437-443
    • Pommer, H.1
  • 22
    • 0032558647 scopus 로고    scopus 로고
    • Water-soluble phosphines enable facile separation of the phosphine oxide by-product, see
    • Water-soluble phosphines enable facile separation of the phosphine oxide by-product, see: M. G. Russell, S. Warren, Tetrahedron Lett. 1998, 39, 7995-7998.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 7995-7998
    • Russell, M.G.1    Warren, S.2
  • 26
    • 85021039010 scopus 로고    scopus 로고
    • CRC Handbook of Chemistry and Physics, 84th Ed. (Ed.: D. R. Lide), 2003-2004, CRC Press, Boca Raton, USA
    • CRC Handbook of Chemistry and Physics, 84th Ed. (Ed.: D. R. Lide), 2003-2004, CRC Press, Boca Raton, USA.
  • 29
    • 0037178544 scopus 로고    scopus 로고
    • It is important to state that the use of a "cata-lyst" still requires a stoichiometric reductant. 0]
    • It is important to state that the use of a "cata-lyst" still requires a stoichiometric reductant. 0] Z.-Z. Huang, Y. Tong, J. Org. Chem. 2002, 67, 5320-5326.
    • (2002) J. Org. Chem. , vol.67 , pp. 5320-5326
    • Huang, Z.-Z.1    Tong, Y.2
  • 32
    • 85021044205 scopus 로고    scopus 로고
    • Japanese Patent JP 03209387A 19910912, 1991 (Chem. Abstr. 1991, 116, 83 923). See also further references cited in Ref. [13]
    • Y. Inoue, M. Arai, T. Miyoshi, Japanese Patent JP 03209387A 19910912, 1991 (Chem. Abstr. 1991, 116, 83 923). See also further references cited in Ref. [13].
    • Inoue, Y.1    Arai, M.2    Miyoshi, T.3
  • 33
    • 20844454091 scopus 로고    scopus 로고
    • and references therein. Similar Lewis-base activation is operative in Denmark's aldol reactions of chlorosilyl enolates, see
    • Similar Lewis-base activation is operative in Denmark's aldol reactions of chlorosilyl enolates, see: S. E. Denmark, Y. Fan, M. D. Eastgate, J. Org. Chem. 2005, 70, 5235-5248, and references therein.
    • (2005) J. Org. Chem. , vol.70 , pp. 5235-5248
    • Denmark, S.E.1    Fan, Y.2    Eastgate, M.D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.