TY  - JOUR
A1  - Wolf, Günter
A1  - Berndt, Heinz
A1  - Brandenburg, Dietrich
T1  - Synthese der [LysA13] Rinderinsulin-A-Kette in der Form [Lys(Tfa)A13]A(SO3H)4 und NαA1-Msc-[LysA13]A(SO3H)4 unter Verwendung des S-tert-Butylmercapto-Restes als Thiolschutzgruppe
JF  - Hoppe-Seyler's Zeitschrift für physiologische Chemie
Y1  - 1979
U6  - http://dx.doi.org/10.1515/bchm2.1979.360.2.1569
SN  - 1437-4315
SN  - 0018-4888
VL  - 360
IS  - 2
SP  - 1569
EP  - 1578
ER  - 
TY  - JOUR
A1  - Gielen, Hans-Günther
A1  - Wolf, Günter
A1  - Berndt, Heinz
A1  - Zahn, Helmut
T1  - Synthese der Fragmente A1–8, A9–15 und A16–21 der Schafinsulin-A-Kette unter Verwendung des S-tert-Butylmercaptorestes als Thiolschutzgruppe
JF  - Hoppe-Seyler's Zeitschrift für physiologische Chemie
Y1  - 1979
U6  - http://dx.doi.org/10.1515/bchm2.1979.360.2.1535
SN  - 1437-4315
SN  - 0018-4888
VL  - 360
IS  - 2
SP  - 1535
EP  - 1548
ER  - 
TY  - JOUR
A1  - Berndt, Heinz
T1  - Synthese der Sequenz 71—86 des Humanproinsulins, I : Synthese der Sequenz 71—86 als monomeres cyclisches Biscystinpeptidderivat und als Tetra-S-tritylderivat
JF  - Hoppe-Seyler's Zeitschrift für physiologische Chemie
Y1  - 1979
U6  - http://dx.doi.org/10.1515/bchm2.1979.360.1.747
SN  - 1437-4315
SN  - 0018-4888
VL  - 360
IS  - 1
SP  - 747
EP  - 760
ER  - 
TY  - JOUR
A1  - Berndt, Heinz
T1  - Synthese der Sequenz 71—86 des Humanproinsulins, III : Synthese über die Fragmente 71—78 und 79—86
JF  - Hoppe-Seyler's Zeitschrift für physiologische Chemie
Y1  - 1979
U6  - http://dx.doi.org/10.1515/bchm2.1979.360.1.765
SN  - 1437-4315
SN  - 0018-4888
VL  - 360
IS  - 1
SP  - 765
EP  - 772
ER  - 
TY  - JOUR
A1  - Wolf, Wilhelm
A1  - Berndt, Heinz
A1  - Brandenburg, Dietrich
T1  - Synthese von Fragmenten einer [LysA13] Rinder-Insulin-A-Kette unter Verwendung des S-tert-Butylmercaptorestes als Thiolschutz
JF  - Hoppe-Seyler's Zeitschrift für physiologische Chemie
Y1  - 1979
U6  - http://dx.doi.org/10.1515/bchm2.1979.360.2.1549
SN  - 1437-4315
SN  - 0018-4888
VL  - 360
IS  - 2
SP  - 1549
EP  - 1558
ER  - 
TY  - BOOK
A1  - Jeromin, Günter Erich
T1  - Synthesen und chemische Eigenschaften einiger 1-Oxo-1H-pyrrolizine [Oxo-H-pyrrolizine] sowie des 1-Oxo-1H-pyrrolizins [Oxo-H-pyrrolizins]
Y1  - 1981
N1  - Heidelberg, Univ., Diss., 1981
ER  - 
TY  - JOUR
A1  - Meyer-Stork, L. Sebastian
A1  - Höcker, Hartwig
A1  - Berndt, Heinz
T1  - Syntheses and reactions of urethanes of cellobiose and cellulose-containing uretdione groups
JF  - Journal of applied polymer science
Y1  - 1992
SN  - 1097-4628
VL  - 44
IS  - 6
SP  - 1043
EP  - 1049
ER  - 
TY  - CHAP
A1  - Berndt, Heinz
A1  - Turck, Christoph W.
ED  - Voelter, Wolfgang
T1  - Syntheses of defined peptide derivatives by aminolysis of 3-[Nα-benzyloxycarbonyl peptidyloxy] -2-hydroxy-N-methyl-benzamides at elevated temperatures II. Synthesis of the peptide derivatives Z-Ala-X-Gly-N(Et)2, X=Phe, Leu, Val, Ser (But), Glu (OBut)
T2  - Chemistry of peptides and proteins : proceedings of the Fourth USSR-FRG Symposium, Tübingen, Federal Republic of Germany, June 8 - 12, 1982 / ed. Wolfgang Voelter ... - Vol. 2
Y1  - 1984
SN  - 3-11009-580-7
SP  - 97
EP  - 103
PB  - de Gruyter
CY  - Berlin [u.a.]
ER  - 
TY  - JOUR
A1  - Pellegrini, Paul A.
A1  - Howell, Nicholas R.
A1  - Shepherd, Rachael K.
A1  - Lengkeek, Nigel A.
A1  - Paulßen, Elisabeth
A1  - Katsifis, Andrew G.
A1  - Greguric, Ivan
T1  - Synthesis and Radiolabelling of DOTA-Linked Glutamine Analogues with 67,68Ga as Markers for Increased Glutamine Metabolism in Tumour Cells
JF  - Molecules
Y1  - 2013
U6  - http://dx.doi.org/10.3390/molecules18067160
SN  - 1420-3049
VL  - 18
IS  - 6
SP  - 7160
EP  - 7178
PB  - MDPI
CY  - Basel
ER  - 
TY  - JOUR
A1  - Immel, Timo
A1  - Grützke, Martin
A1  - Späte, Anne-Katrin
A1  - Groth, Ulrich
A1  - Öhlschläger, Peter
A1  - Huhn, Thomas
T1  - Synthesis and X-ray structure analysis of a heptacoordinate titanium(IV)-bis-chelate with enhanced in vivo antitumor efficacy
JF  - Chemical Communications
N2  - Chelate stabilization of a titanium(IV)–salan alkoxide by ligand exchange with 2,6-pyridinedicarboxylic acid (dipic) resulted in heptacoordinate complex 3 which is not redox-active, stable on silica gel and has increased aqueous stability. 3 is highly toxic in HeLa S3 and Hep G2 and has enhanced antitumor efficacy in a mouse cervical-cancer model.
Y1  - 2012
U6  - http://dx.doi.org/10.1039/C2CC31624B
SN  - 1364-548X
VL  - 48
IS  - 46
SP  - 5790
EP  - 5792
PB  - Royal Society of Chemistry
CY  - Cambridge
ER  -