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K. MUELLER

Observed names: K.‐H. + MUELLER, Karoline Mueller, Mueller, Karoline
OpenAlex ID: A5112508343
Synthesis, characterization, structures and in vitro antitumor activity of platinum(II) complexes bearing adeninato or methylated adeninato ligands
2020 · Karoline Mueller, Christina Schütz, et al. · Inorganica Chimica Acta · 3
ChemInform Abstract: A New General Approach to Enantiomerically Pure Cyclic and Open‐Chain ( R)‐ and (S)‐α,α‐Disubstituted α‐Amino Acids.
1992 · D. OBRECHT, C. SPIEGLER, et al. · ChemInform · 3
ChemInform Abstract: Novel Open‐Chain and Cyclic Conformationally Constrained (R)‐ and (S)‐. alpha.,α‐Disubstituted Tyrosine Analogues.
1995 · D. OBRECHT, C. LEHMANN, et al. · ChemInform · 2
ChemInform Abstract: An Efficient Synthesis of Optically Pure (R)‐ and (S)‐2‐(Aminomethyl) alanine ((R)‐ and (S)‐Ama) and (R)‐ and (S)‐2‐(Aminomethyl)leucine ((R) ‐ and (S)‐Aml).
1995 · D. OBRECHT, H. KARAJIANNIS, et al. · ChemInform · 2
ChemInform Abstract: L‐Phenylalanine Cyclohexylamide: A Simple and Convenient Auxiliary for the Synthesis of Optically Pure α,α‐Disubstituted (R)‐ and (S)‐Amino Acids.
1995 · D. OBRECHT, U. BOHDAL, et al. · ChemInform · 1
ChemInform Abstract: Synthesis of Enantiomerically Pure D‐ and L‐(Heteroaryl)alanines by Asymmetric Hydrogenation of (Z)‐α‐Amino‐α,β‐didehydro Esters.
1994 · T. MASQUELIN, E. BROGER, et al. · ChemInform · 1
CCDC 1949976: Experimental Crystal Structure Determination
2020 · Mueller, Karoline, Schütz, Christina, et al. · The Cambridge Structural Database
CCDC 1949975: Experimental Crystal Structure Determination
2020 · Mueller, Karoline, Schütz, Christina, et al. · The Cambridge Structural Database
CCDC 1949974: Experimental Crystal Structure Determination
2020 · Mueller, Karoline, Schütz, Christina, et al. · The Cambridge Structural Database
CCDC 1949977: Experimental Crystal Structure Determination
2020 · Mueller, Karoline, Schütz, Christina, et al. · The Cambridge Structural Database
ChemInform Abstract: Synthesis, Conformational Properties, and Synthetic Applications of Novel Optically Pure α,α‐Disubstituted (R)‐ and (S)‐ Glycines (“α‐Chimeras”) Combining Side Chains of Asp, Glu, Leu, Phe, Ser, and Val.
1996 · D. OBRECHT, C. ABRECHT, et al. · ChemInform
ChemInform Abstract: An Efficient Strategy to Orthogonally Protected (R)‐ and (S)‐α‐ Methyl(alkyl)serine‐Containing Peptides via a Novel Azlactone/ Oxazoline Interconversion Reaction.
1996 · D. OBRECHT, M. ALTORFER, et al. · ChemInform
ChemInform Abstract: A Novel Synthesis of (R)‐ and (S)‐α‐Alkylated Aspartic and Glutamic Acids: α‐Alkylated Aspartic Succinimides as New Type of β‐Turn Type II and II′ Mimetics.
1996 · D. OBRECHT, U. BOHDAL, et al. · ChemInform
ChemInform Abstract: A Reinvestigation of the α‐Alkylation of 4‐Monosubstituted 2‐ Phenyloxazol‐5(4H)‐ones (Azlactones): A General Entry into Highly Functionalized α,α‐Disubstituted α‐Amino Acids.
1994 · D. OBRECHT, U. BOHDAL, et al. · ChemInform
ChemInform Abstract: Liquid Crystalline Derivatives of Cyclohexane with Lateral Substituents in the Middle Group.
1994 · H.‐J. DEUTSCHER, K. MUELLER, et al. · ChemInform
ChemInform Abstract: Liquid Crystals with Aliphatic Groups Between Cyclohexane Rings. Synthesis of 1,4‐Bis(4‐n‐alkylcyclohexyl)butanes and Esters of 4‐(4‐(4‐ n‐Alkylcyclohexyl)butyl)cyclohexanols.
1993 · H.‐J. DEUTSCHER, K. MUELLER, et al. · ChemInform
ChemInform Abstract: cis‐/trans‐(1.1.1)‐Trithia‐ and trans‐(4.4.4)‐Hexathia‐tris‐σ‐homobenzenes.
1988 · S. KAGABU, C. KAISER, et al. · ChemInform
ChemInform Abstract: “CIS‐TRIAZATRIS‐Σ‐HOMOBENZENES” (“CIS‐BENZENE TRIIMINE”). SYNTHESES AND (Σ2S + Σ2S + Σ2S) CYCLOREVERSIONS TO 4,7‐DIHYDRO‐1H‐1,4,7‐TRIAZONINES
1981 · R. SCHWESINGER, M. BREUNINGER, et al. · ChemInform
ChemInform Abstract: CIS‐OXA,AZA‐Σ‐HOMOBENZENES. SYNTHESIS AND (2+2+2)‐CYCLOREVERSION REACTIONS
1980 · H. PRINZBACH, K.‐H. + MUELLER, et al. · ChemInform
ChemInform Abstract: 1,4‐DIHYDRO‐1,4‐DIAZOCINE; NITROGEN SUBSTITUTION AND STRUCTURE (“AROMATICITY”)
1980 · M. BREUNINGER, B. GALLENKAMP, et al. · ChemInform
Works count: 20
Citation count: 12
H-index: 2
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