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Volumn 40, Issue 46, 1999, Pages 8181-8184

A Horner-Wadsworth-Emmons approach to dipolar and non-dipolar poly(phenylenevinylene)dendrimers

Author keywords

[No Author keywords available]

Indexed keywords

DENDRIMER; OLIGOMER;

EID: 0033550277     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)01733-5     Document Type: Article
Times cited : (31)

References (30)
  • 9
    • 0001606120 scopus 로고    scopus 로고
    • a) Morgenroth, F.; Mullen, K. Tetrahedron 1997, 53, 15439, and Angew. Chem. Int. Ed. Engl. 1997, 36, 631.
    • (1997) Tetrahedron , vol.53 , pp. 15439
    • Morgenroth, F.1    Mullen, K.2
  • 10
    • 0030948203 scopus 로고    scopus 로고
    • a) Morgenroth, F.; Mullen, K. Tetrahedron 1997, 53, 15439, and Angew. Chem. Int. Ed. Engl. 1997, 36, 631.
    • (1997) Angew. Chem. Int. Ed. Engl. , vol.36 , pp. 631
  • 24
    • 0001169001 scopus 로고
    • 4 (Ashton, P. R.; Shibata, K.; Shipway, A. N.; Stoddart, J.F. Angew. Chem. Int. Ed. Engl. 1997, 36, 2781) have also been reported to proceed in good yields. 1,3,5-tris(hydroxymethylbenzene) was prepared by reduction with lithium aluminium hydride in refluxing THF of the commercially available 1,3,5-trimethyl benzenetricarboxylate according to a modification of the procedure reported by Cochrane, W P.; Pauson, P. L., Stevens, T. S. J. Chem. Soc. (C) 1968, 630.
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 3201
    • Boekelheide, V.1    Hollins, R.A.2
  • 25
    • 0032491868 scopus 로고    scopus 로고
    • have also been reported to proceed in good yields
    • 4 (Ashton, P. R.; Shibata, K.; Shipway, A. N.; Stoddart, J.F. Angew. Chem. Int. Ed. Engl. 1997, 36, 2781) have also been reported to proceed in good yields. 1,3,5-tris(hydroxymethylbenzene) was prepared by reduction with lithium aluminium hydride in refluxing THF of the commercially available 1,3,5-trimethyl benzenetricarboxylate according to a modification of the procedure reported by Cochrane, W P.; Pauson, P. L., Stevens, T. S. J. Chem. Soc. (C) 1968, 630.
    • (1997) Angew. Chem. Int. Ed. Engl. , vol.36 , pp. 2781
    • Ashton, P.R.1    Shibata, K.2    Shipway, A.N.3    Stoddart, J.F.4
  • 26
    • 37049129544 scopus 로고
    • 4 (Ashton, P. R.; Shibata, K.; Shipway, A. N.; Stoddart, J.F. Angew. Chem. Int. Ed. Engl. 1997, 36, 2781) have also been reported to proceed in good yields. 1,3,5-tris(hydroxymethylbenzene) was prepared by reduction with lithium aluminium hydride in refluxing THF of the commercially available 1,3,5-trimethyl benzenetricarboxylate according to a modification of the procedure reported by Cochrane, W P.; Pauson, P. L., Stevens, T. S. J. Chem. Soc. (C) 1968, 630.
    • (1968) J. Chem. Soc. (C) , pp. 630
    • Cochrane, W.P.1    Pauson, P.L.2    Stevens, T.S.3
  • 27
    • 0009534308 scopus 로고    scopus 로고
    • Although the presence of starting material 1 as well as the corresponding triacetate was also observed in the crude mixture, all the products were easily separated by column chromatography
    • Although the presence of starting material 1 as well as the corresponding triacetate was also observed in the crude mixture, all the products were easily separated by column chromatography.
  • 30
    • 0009502539 scopus 로고    scopus 로고
    • 3)
    • 3).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.