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NEW REAGENTS SUPPRESSING RACEMIZATION IN PEPTIDE SYNTHESIS BY THE DCC METHODIZDEBSKI J.1979; POLISH J. CHEM.; POL; DA. 1979; VOL. 53; NO 5; PP. 1049-1057; ABS. POL; BIBL. 16 REF.Article

AN IMPROVEMENT OF THE YOUNG TEST. INVESTIGATIONS ON OPTICAL AND CHEMICAL PURITY OF A PRODUCT OF PEPTIDE COUPLING OBTAINED BY THE DCC AND ADDITIVES METHODIZDEBSKI J.1975; ROCZ. CHEM.; POLSKA; DA. 1975; VOL. 49; NO NO 6; PP. 1097-1104; ABS. POL. RUSSE; BIBL. 33 REF.Article

La situation militaire entre la Vistule et le Bug après le 15.9.1939IZDEBSKI, J.Wojskowy Przegląd Historyczny. 1991, Vol 36, Num 2, pp 70-80Article

FORMATION OF N-ACYL DERIVATIVES OF N,N'-DISUBSTITUTED UREA IN THE REACTION OF PEPTIDE BOND FORMATION BY THE CARBODIIMIDE METHOD. II. REACTIONS OF CARBOBENZOXY AMINO ACIDS WITH GLYCINE ETHYL ESTER.IZDEBSKI J; LEBEK M; DRABAREK S et al.1977; ROCZ. CHEM.; POLSKA; DA. 1977; VOL. 51; NO 1; PP. 81-88; ABS. POL. RUSSE; BIBL. 12 REF.Article

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. I. REACTIONS OF N-DERIVATIVES OF GLYCINEIZDEBSKI J; DRABAREK S; LEBEK M et al.1975; ROCZ. CHEM.; POLSKA; DA. 1975; VOL. 49; NO 9; PP. 1535-1540; ABS. POL. RUSSE; BIBL. 15 REF.Article

SYNTHESIS AND PROPERTIES OF EQUINE BETA -MELANOTROPIN AND ITS NATURALLY OCCURRING DES-ASP ANALOGIZDEBSKI J; YAMASHIRO D; TZI BUN NG et al.1982; INT. J. PEPT. PROTEIN RES.; ISSN 0367-8377; DNK; DA. 1982; VOL. 19; NO 4; PP. 327-333; BIBL. 28 REF.Article

IMAGE ANGIOGRAPHIQUE DE LA VESICULE BILIAIREBIEGANOWSKA KLAMUT Z; KLAMUT M; KOZIOL T et al.1974; ANN. UNIV. MARIAE CURIE-SKLODOWSKA, D; POLOGNE; DA. 1974; VOL. 29; PP. 127-133; H.T. 7; ABS. RUSSE ANGL.; BIBL. 11REF.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

Primary structure of fox pituitary growth hormoneCHOH HAO LI; IZDEBSKI, J; CHUNG, D et al.International journal of peptide & protein research. 1989, Vol 33, Num 1, pp 70-72, issn 0367-8377Article

1-Cyclohexyl-2-cyclohexylamino-5(4H)-imidazoloneANULEWICZ, R; FIERTEK, D; IZDEBSKI, J et al.Acta crystallographica. Section C, Crystal structure communications. 1995, Vol 51, pp 541-543, issn 0108-2701, 3Article

Sequence dependence in the formation of pyroglutamyl peptides in solid phase peptide synthesisORŁOWSKA, A; WITKOWSKA, E; IZDEBSKI, J et al.International journal of peptide & protein research. 1987, Vol 30, Num 1, pp 141-144, issn 0367-8377Article

Isolation and amino acid sequence of insulins and C-peptides of European bison (Bison bonasus) and fox (Alopex lagopus)MAJEWSKI, T; THIM, L; IZDEBSKI, J et al.International journal of peptide & protein research. 1987, Vol 30, Num 3, pp 379-387, issn 0367-8377Article

High-pressure synthesis of 5.6-dihydro-2H-pyran system. Eu(FOD)3 mediated (4+2)cycloaddition of 1-methoxybuta-1,3-diene to N-protected α-amino aldehydesGOłEBIOWSKI, A; IZDEBSKI, J; JACOBSSON, U et al.Heterocycles (Sendai). 1986, Vol 24, Num 5, pp 1205-1208, issn 0385-5414Article

Immobilized metal-ion affinity chromatography of peptides on metalloporphyrin stationary phasesBIESAGA, M; ORSKA, J; FIERTEK, D et al.Fresenius' journal of analytical chemistry. 1999, Vol 364, Num 1-2, pp 160-164, issn 0937-0633Article

Reinvestigation of the reactions of carbodiimides with alkoxycarbonylamino acid symmetrical anhydridesIZDEBSKI, J; ORŁOWSKA, A; ANULEWICZ, R et al.International journal of peptide & protein research. 1994, Vol 43, Num 2, pp 184-189, issn 0367-8377Article

Synthesis and biological evaluation of human preproenkephalin (100-111) and its analogsIZDEBSKI, J; BONDARUK, J; GUMULKA, S. W et al.International journal of peptide & protein research. 1989, Vol 33, Num 2, pp 77-81, issn 0367-8377Article

Synthesis and properties of equine β-melanotropin analogs with substitution in residue position 1NADASDI, L; YAMASHIRO, D; CHOH HAO LI et al.International journal of peptide & protein research. 1983, Vol 21, Num 4, pp 364-368, issn 0367-8377Article

Postexercise decrease in arterial blood pressure, total peripheral resistance and in circulatory responses to brief hyperoxia in subjects with mild essential hypertensionIZDEBSKA, E; CYBULSKA, I; SAWICKI, M et al.Journal of human hypertension. 1998, Vol 12, Num 12, pp 855-860, issn 0950-9240Article

Isolation and characterization of growth hormone from blue fox pituitary glandsLI, C. H; CHUNG, D; IZDEBSKI, J et al.International journal of peptide & protein research. 1988, Vol 31, Num 2, pp 201-204, issn 0367-8377Article

Effect of chronic administration of a new potent agonist of GH-RH(1-29)NH2 on linear growth and GH responsiveness in ratsPINSKI, J; IZDEBSKI, J; JUNGWIRTH, A et al.Regulatory peptides. 1996, Vol 65, Num 3, pp 197-201, issn 0167-0115Article

Methylene chloride-soluble and insoluble ureines: an X-ray diffraction, infrared absorption, and proton magnetic resonance studyTONIOLO, C; VALLE, G; BONORA, G. M et al.International journal of peptide & protein research. 1988, Vol 31, Num 1, pp 77-85, issn 0367-8377Article

(Cholestanyloxycarbonyl)benzyl esters as peptide substituents: conformational properties of fully protected oligo-L-lysines with C-terminal (cholestanyloxycarbonyl)benzyl and benzyl ester moietiesTONIOLO, C; BONORA, G. M; MORETTO, V et al.Helvetica chimica acta. 1986, Vol 69, Num 2, pp 350-358, issn 0018-019XArticle

64. N-acylureas in peptide synthesis : an X-Ray diffraction an IR-absorption studyTONIOLO, C; VALLE, G; CRISMA, M et al.Helvetica chimica acta. 1990, Vol 73, Num 3, pp 626-634, issn 0018-019X, 9 p.Article

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