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http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44/issue_13/101021jm000979z/authorship/6
http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_21/101021jo030131t/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/1996/volume_39/issue_20/101021jm960341g/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/1998/volume_41/issue_21/101021jm980121y/authorship/2
http://hub.abes.fr/springer/periodical/706/1994/volume_125/issue_11/B8CEC1B32BC83A9AE053120B220A9C63/authorship/1
http://hub.abes.fr/springer/periodical/706/1986/volume_117/issue_2/B8CEC1B331023A9AE053120B220A9C63/authorship/2
http://hub.abes.fr/springer/periodical/706/1991/volume_122/issue_12/B8CEC1B32E713A9AE053120B220A9C63/authorship/2
http://hub.abes.fr/springer/periodical/706/1995/volume_126/issue_6_7/B8CF0062032F7E97E053120B220A3B7C/authorship/2
http://hub.abes.fr/springer/periodical/706/1990/volume_121/issue_10/B8CF0062006B7E97E053120B220A3B7C/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/1992/volume_35/issue_17/101021jm00095a027/authorship/3
http://hub.abes.fr/springer/periodical/706/1988/volume_119/issue_2/B8CBE6EA00452F91E053120B220A16B6/authorship/2
http://hub.abes.fr/springer/periodical/706/1992/volume_123/issue_11/B8CE95BE6E333A8CE053120B220AD92C/authorship/1
http://hub.abes.fr/springer/periodical/706/1992/volume_123/issue_12/B8CE95BE6E723A8CE053120B220AD92C/authorship/1
http://hub.abes.fr/springer/periodical/706/1987/volume_118/issue_3/B8CE95BE6CDE3A8CE053120B220AD92C/authorship/2
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On the chemistry of pyrazolylalkines; pyrazoles II
On the structure of guanylhydrazones derived from aromatic aldehydes
Pyridazines, LVIII: 1-Phenyl-1-pyridazinyl-2-substituted ethenes, synthesis and configuration
On the Bioisosteric Potential of Diazines: Diazine Analogues of the CombinedThromboxane A2 Receptor Antagonist and Synthetase Inhibitor Ridogrel
Substituted 4-Acylpyrazoles and 4-Acylpyrazolones: Synthesis and MultidrugResistance-Modulating Activity
On the reaction of diethyl 3,4-dihydroxythiophene-2,5-dicarboxylate with 1,2-dibromoethane
Spiro-Fused (C2)-Azirino-(C4)-pyrazolones, a New HeterocyclicSystem. Synthesis, Spectroscopic Studies and X-ray StructureAnalysis1
On the application of homonuclear NOE difference spectroscopy as a convenient tool for configurational assignment of compounds with a C=N bond
Synthesis, Cytotoxicity, and Antitumor Activity of Copper(II) and Iron(II)Complexes of 4N-Azabicyclo[3.2.2]nonane Thiosemicarbazones Derived fromAcyl Diazines
The structure of the product obtained by the reaction of 2-hydroximino-3-oxo-5-phenyl-4-pentenenitrile with ethylcyanoacetate
1,4-Diacyl-3-acylamino-5-aryl-4,5-dihydro-1H-1,2,4-triazoles: Ring closure products of aromatic carbaldehyde (diaminomethylene) hydrazones with acylating agents
Pyridazines. 63. Novel thiosemicarbazones derived from formyl- and acyldiazines: synthesis, effects on cell proliferation, and synergism with antiviral agents
Reactions of 4,5-unsaturated 3-oxoalkanenitriles withMichael acceptors
On the discrimination of tetrazole regioisomers by NOE difference spectroscopy
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