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Volumn 4, Issue 4-6, 1997, Pages 341-349

Design and synthesis of chiral peptidic nucleic acids

Author keywords

Antisense therapy; Chiral oligonucleotide analogues; Fmoc C PNA amino acids; Fmoc chemistry; Solid phase synthesis

Indexed keywords


EID: 0000615793     PISSN: 09295666     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF02442898     Document Type: Article
Times cited : (8)

References (19)
  • 8
    • 33644477832 scopus 로고
    • Some selected examples: a. Egholm, M., Buchardt, O., Nielsen, P.E. and Berg, R.H., J. Am. Chem. Soc., 114 (1992) 1895. b. Thomson, S.A., Josey, J.A., Cadilla, R., Gaul, M.D., Hassman, C.F., Luzzio, M.J., Pipe, A.J., Reed, K.L., Ricca, D.J., Wiethe, R.W. and Noble, S.A., Tetrahedron, 51 (1995) 6179. c. Petersen, K.H., Buchardt, O. and Nielsen, P.E., Bioorg. Med. Chem. Lett., 6 (1996) 793. d. Savitri, D., Leumann, C. and Scheffold, R., Helv. Chim. Acta, 79 (1996) 288. e. Fujii, M., Yamamoto, K., Hidaka, J. and Ohtsu, T., Tetrahedron Lett., 38 (1997) 417. f. Lioy, E. and Kessler, H., Liebigs Ann., (1996) 201.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 1895
    • Egholm, M.1    Buchardt, O.2    Nielsen, P.E.3    Berg, R.H.4
  • 9
    • 0029044163 scopus 로고
    • Some selected examples: a. Egholm, M., Buchardt, O., Nielsen, P.E. and Berg, R.H., J. Am. Chem. Soc., 114 (1992) 1895. b. Thomson, S.A., Josey, J.A., Cadilla, R., Gaul, M.D., Hassman, C.F., Luzzio, M.J., Pipe, A.J., Reed, K.L., Ricca, D.J., Wiethe, R.W. and Noble, S.A., Tetrahedron, 51 (1995) 6179. c. Petersen, K.H., Buchardt, O. and Nielsen, P.E., Bioorg. Med. Chem. Lett., 6 (1996) 793. d. Savitri, D., Leumann, C. and Scheffold, R., Helv. Chim. Acta, 79 (1996) 288. e. Fujii, M., Yamamoto, K., Hidaka, J. and Ohtsu, T., Tetrahedron Lett., 38 (1997) 417. f. Lioy, E. and Kessler, H., Liebigs Ann., (1996) 201.
    • (1995) Tetrahedron , vol.51 , pp. 6179
    • Thomson, S.A.1    Josey, J.A.2    Cadilla, R.3    Gaul, M.D.4    Hassman, C.F.5    Luzzio, M.J.6    Pipe, A.J.7    Reed, K.L.8    Ricca, D.J.9    Wiethe, R.W.10    Noble, S.A.11
  • 10
    • 0029981505 scopus 로고    scopus 로고
    • Some selected examples: a. Egholm, M., Buchardt, O., Nielsen, P.E. and Berg, R.H., J. Am. Chem. Soc., 114 (1992) 1895. b. Thomson, S.A., Josey, J.A., Cadilla, R., Gaul, M.D., Hassman, C.F., Luzzio, M.J., Pipe, A.J., Reed, K.L., Ricca, D.J., Wiethe, R.W. and Noble, S.A., Tetrahedron, 51 (1995) 6179. c. Petersen, K.H., Buchardt, O. and Nielsen, P.E., Bioorg. Med. Chem. Lett., 6 (1996) 793. d. Savitri, D., Leumann, C. and Scheffold, R., Helv. Chim. Acta, 79 (1996) 288. e. Fujii, M., Yamamoto, K., Hidaka, J. and Ohtsu, T., Tetrahedron Lett., 38 (1997) 417. f. Lioy, E. and Kessler, H., Liebigs Ann., (1996) 201.
    • (1996) Bioorg. Med. Chem. Lett. , vol.6 , pp. 793
    • Petersen, K.H.1    Buchardt, O.2    Nielsen, P.E.3
  • 11
    • 0030058035 scopus 로고    scopus 로고
    • Some selected examples: a. Egholm, M., Buchardt, O., Nielsen, P.E. and Berg, R.H., J. Am. Chem. Soc., 114 (1992) 1895. b. Thomson, S.A., Josey, J.A., Cadilla, R., Gaul, M.D., Hassman, C.F., Luzzio, M.J., Pipe, A.J., Reed, K.L., Ricca, D.J., Wiethe, R.W. and Noble, S.A., Tetrahedron, 51 (1995) 6179. c. Petersen, K.H., Buchardt, O. and Nielsen, P.E., Bioorg. Med. Chem. Lett., 6 (1996) 793. d. Savitri, D., Leumann, C. and Scheffold, R., Helv. Chim. Acta, 79 (1996) 288. e. Fujii, M., Yamamoto, K., Hidaka, J. and Ohtsu, T., Tetrahedron Lett., 38 (1997) 417. f. Lioy, E. and Kessler, H., Liebigs Ann., (1996) 201.
    • (1996) Helv. Chim. Acta , vol.79 , pp. 288
    • Savitri, D.1    Leumann, C.2    Scheffold, R.3
  • 12
    • 0031032862 scopus 로고    scopus 로고
    • Some selected examples: a. Egholm, M., Buchardt, O., Nielsen, P.E. and Berg, R.H., J. Am. Chem. Soc., 114 (1992) 1895. b. Thomson, S.A., Josey, J.A., Cadilla, R., Gaul, M.D., Hassman, C.F., Luzzio, M.J., Pipe, A.J., Reed, K.L., Ricca, D.J., Wiethe, R.W. and Noble, S.A., Tetrahedron, 51 (1995) 6179. c. Petersen, K.H., Buchardt, O. and Nielsen, P.E., Bioorg. Med. Chem. Lett., 6 (1996) 793. d. Savitri, D., Leumann, C. and Scheffold, R., Helv. Chim. Acta, 79 (1996) 288. e. Fujii, M., Yamamoto, K., Hidaka, J. and Ohtsu, T., Tetrahedron Lett., 38 (1997) 417. f. Lioy, E. and Kessler, H., Liebigs Ann., (1996) 201.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 417
    • Fujii, M.1    Yamamoto, K.2    Hidaka, J.3    Ohtsu, T.4
  • 13
    • 33748890087 scopus 로고    scopus 로고
    • Some selected examples: a. Egholm, M., Buchardt, O., Nielsen, P.E. and Berg, R.H., J. Am. Chem. Soc., 114 (1992) 1895. b. Thomson, S.A., Josey, J.A., Cadilla, R., Gaul, M.D., Hassman, C.F., Luzzio, M.J., Pipe, A.J., Reed, K.L., Ricca, D.J., Wiethe, R.W. and Noble, S.A., Tetrahedron, 51 (1995) 6179. c. Petersen, K.H., Buchardt, O. and Nielsen, P.E., Bioorg. Med. Chem. Lett., 6 (1996) 793. d. Savitri, D., Leumann, C. and Scheffold, R., Helv. Chim. Acta, 79 (1996) 288. e. Fujii, M., Yamamoto, K., Hidaka, J. and Ohtsu, T., Tetrahedron Lett., 38 (1997) 417. f. Lioy, E. and Kessler, H., Liebigs Ann., (1996) 201.
    • (1996) Liebigs Ann. , pp. 201
    • Lioy, E.1    Kessler, H.2
  • 17
    • 2342623512 scopus 로고    scopus 로고
    • note
    • A well detailed study about the racemisation of the first procedure and the analysis of the enantiomeric purity of the final products will be published in a separate letter.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.