References
- Allen , J. G. , Atherton , F. R. , Hall , M. J. , Hassall , C. H. , Holmes , S. W. , Lambert , R. W. , Nisbet , L. J. and Ringrose , P. S. 1978 . Nature , 272 : 56
- Mastalerz , P. , Kupczyk-Subotkowska , L. , Herman , Z. S. and Laskawiec , G. 1982 . Naturwissenschaften , 69 : 46
- Gancarz , R. , Kafarski , P. , Lejczak , B. , Mastalerz , P. , Wieczorek , J. S. , Przybylka , E. and Czerwinski , W. 1983 . Phosphorus and Sulfur , 18 : 373
- Bloom , R. S. 1981 . “Peptides, Synthesis-Function” , Proceedings of the Seventh American Peptide Symposium Edited by: Rich , D. H. and Gross , E. 577
- Frohman , C. E. German, Patent 2 712 781 .
- 1978 . C. A. , 88 : 170493x
- Richardson , S. D. 1980 . Virology , 105 : 205
- Walter , R. 1979 . Proc. Natl. Acad. Sci. USA , 76 : 518
- Kafarski , P. , Lejczak , B. and Mastelerz , P. 1985 . Beitr. Wirkstofforsch. ,
- Kametani , T. , Kigasawa , K. , Hiiragi , M. , Wakisaka , K. , Haga , S. , Sugi , H. , Tanigawa , K. , Suzuki , Y. , Fukawa , K. , Irino , O. , Saita , O. and Yamabe , S. 1981 . Heterocycles , 16 : 1205
- Atherton , F. R. , Hassall , C. H. and Lambert , R. W. 1986 . J. Med. Chem. , 29 : 29
- Atherton , F. R. , Hall , M. J. , Hassall , C. H. , Lambert , R. W. and Ringrose , P. S. German Patent 2 602 193 . 1976 .
- 1976 . C. A. , 85 : 143525
- Rabinowitz , R. 1963 . J. Org. Chem. , 28 : 2975
- Maier , L. 1979 . J. Organomet. Chem. , 178 : 157
- Birkofer , L. , Ritter , A. and Neuhausen , P. 1962 . Liebigs Ann. Chem. , : 190
- Kafarski , P. , Soroka , M. and Lejczak , B. 1988 . Peptide Chemistry 1987 , Edited by: Shiba , T. and Sakakibara , S. 307 Osaka : Protein Research Foundation .
- 1988 . C. A. , 109 : 170892d When this work was in propress, the communications of Polish authors, was published, where silylated aminophosphonic acids were reported to be used for the synthesis of totally unblocked phosphonodipeptides. However, N-acylated phosphonopetides with free phosphonic group were not described in this communication
- Kudzin , Z. H. and Stec , W. J. 1978 . Synthesis , : 469
- Pulwer , M. J. and Balthazor , T. M. 1986 . Synth. Commun. , 16 : 733
- Kafarski , P. and Lejczak , B. 1988 . Synthesis , : 307
- Satisfactory microanalyses were obtained: P ± 0.10, Si ± 0.29
- Satisfactory microanlyses were obtained: C ± 0.48, H ± 0.30, N ± 0.38, P ± 0.29. Compounds 3bc, e, f are the mixtures of two diastereomers
- N-Deprotection of 3b affords the mixture of two diastereomeric phosphonopetides, which are distinctly distinguishable in NMR-31P-{1H} spectrum (Δ δP 0.12 ppm)