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Volumn 5, Issue 8, 2000, Pages 1018-1032

Exploiting poly(ethylene glycol) as a matrix for liquid-phase organic synthesis

Author keywords

Poly(ethylene glycol); Soluble polymer; Stille reaction; Synthesis; Triphenyl phosphine; Wittig reaction

Indexed keywords

MACROGOL;

EID: 0001404049     PISSN: 14203049     EISSN: None     Source Type: Journal    
DOI: 10.3390/50801018     Document Type: Article
Times cited : (11)

References (53)
  • 19
    • 0001537043 scopus 로고
    • A recent report attempts the synthesis of 2 for use as a macroinitiator in block copolymer synthesis (Choi, Y.K.; Bae, Y.H.; Kim, S.W. Macromolecules 1995, 28, 8419-8421). However, the authors observed significant oxidation of the phosphine end-groups during its isolation which they did not isolate in pure form.
    • (1995) Macromolecules , vol.28 , pp. 8419-8421
    • Choi, Y.K.1    Bae, Y.H.2    Kim, S.W.3
  • 20
    • 16144366217 scopus 로고    scopus 로고
    • A recent report descibes a one step route to phosphine 6 in moderate yield (63% yield). [Herd, H.; Heßler, A.; Hingst, W.; Tepper, M.; Stelzer, O. Journal of Organometallic Chemistry 1996, 522, 69-76.] However, in our hands the obtained yields were even lower (38%). Therefore we adopted a three step approach to 6 the overall yield being 83% (Scheme 1).
    • (1996) Journal of Organometallic Chemistry , vol.522 , pp. 69-76
    • Herd, H.1    Heßler, A.2    Hingst, W.3    Tepper, M.4    Stelzer, O.5
  • 27
    • 0000677232 scopus 로고
    • Li, C.-J. Chem. Rev. 1993, 93, 2023-2035.
    • (1993) Chem. Rev. , vol.93 , pp. 2023-2035
    • Li, C.-J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.