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FORMATION OF N-ACYL DERIVATIVES OF N,N'-DISUSBSTITUTED UREA IN THE REACTION OF PEPTIDE BOND FORMATION BY THE CARBODIIMIDE METHOD. V: USE OF N,N'-DIISOPROPYLCARBODIIMIDE IN PEPTIDE SYNTHESISIZDEBSKI J; KUNCE D; DRABAREK S et al.1980; POLISH J. CHEM.; POL; DA. 1980; VOL. 54; NO 3; PP. 413-418; ABS. POL; BIBL. 7 REF.Article

FORMATION OF N-ACYL DERIVATIVES OF N,N'-DISUBSTITUTED UREA IN THE REACTION OF PEPTIDE BOND FORMATION BY THE CARBODIIMIDE METHOD. III. REACTIONS OF STERICALLY HINDERED AMINO ACIDS AND AMINO ACIDS WITH FUNCTIONAL GROUPS IN THE SIDE CHAIN.IZDEBSKI J; KUBIAK T; KUNCE D et al.1978; POLISH J. CHEM.; POLAND; DA. 1978; VOL. 52; NO 3; PP. 539-545; ABS. POL.; BIBL. 10 REF.Article

FORMATION OF N-ACYL DERIVATIVES OF N,N'-DISUBSTITUTED UREA IN THE REACTION OF PEPTIDE BOND FORMATION BY THE CARBODIIMIDE METHOD. IV: REACTIONS OF TERT-BUTYLOXYCARBONYL AMINO ACIDS WITH GLYCINE ETHYL ESTERIZDEBSKI I; KUNCE D; PELKA J et al.1980; POLISH J. CHEM.; POL; DA. 1980; VOL. 54; NO 1; PP. 117-120; BIBL. 3 REF.Article

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