J.O. Daiss

526 total citations
20 papers, 431 citations indexed

About

J.O. Daiss is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, J.O. Daiss has authored 20 papers receiving a total of 431 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Organic Chemistry, 8 papers in Molecular Biology and 5 papers in Inorganic Chemistry. Recurrent topics in J.O. Daiss's work include Synthesis and characterization of novel inorganic/organometallic compounds (5 papers), Coordination Chemistry and Organometallics (5 papers) and Organoboron and organosilicon chemistry (4 papers). J.O. Daiss is often cited by papers focused on Synthesis and characterization of novel inorganic/organometallic compounds (5 papers), Coordination Chemistry and Organometallics (5 papers) and Organoboron and organosilicon chemistry (4 papers). J.O. Daiss collaborates with scholars based in Germany, United Kingdom and France. J.O. Daiss's co-authors include Reinhold Tacke, Christian Burschka, John G. Montana, John Mills, Graham A. Showell, J.B.H. Warneck, Hinrich Gronemeyer, Matthew J. Barnes, C. Gaudon and Diana Ivanova and has published in prestigious journals such as Chemistry - A European Journal, Tetrahedron and Toxicology and Applied Pharmacology.

In The Last Decade

J.O. Daiss

20 papers receiving 423 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
J.O. Daiss Germany	12	272	136	75	53	25	20	431
Laurie B. Schenkel United States	13	390 1.4×	125 0.9×	99 1.3×	13 0.2×	77 3.1×	24	582
Chitra Sundararajan United States	16	280 1.0×	288 2.1×	27 0.4×	166 3.1×	44 1.8×	21	660
Finn Burg Germany	10	367 1.3×	37 0.3×	125 1.7×	61 1.2×	10 0.4×	11	436
Cecı́lia P. Sár Hungary	12	131 0.5×	140 1.0×	32 0.4×	84 1.6×	37 1.5×	32	433
Tram H. Hoang United States	8	166 0.6×	87 0.6×	45 0.6×	67 1.3×	14 0.6×	11	309
R. Scott Hoerrner United States	12	551 2.0×	139 1.0×	81 1.1×	36 0.7×	7 0.3×	14	671
Michael G. Vetelino United States	10	459 1.7×	220 1.6×	77 1.0×	40 0.8×	17 0.7×	17	623
Suprabhat Ray India	18	421 1.5×	137 1.0×	72 1.0×	29 0.5×	39 1.6×	58	696
N. Knouzi France	7	334 1.2×	145 1.1×	72 1.0×	41 0.8×	25 1.0×	21	435
C. K. Govindan United States	8	166 0.6×	76 0.6×	17 0.2×	27 0.5×	7 0.3×	10	354

Countries citing papers authored by J.O. Daiss

Since Specialization

Citations

This map shows the geographic impact of J.O. Daiss's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by J.O. Daiss with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites J.O. Daiss more than expected).

Fields of papers citing papers by J.O. Daiss

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J.O. Daiss. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by J.O. Daiss. The network helps show where J.O. Daiss may publish in the future.

Co-authorship network of co-authors of J.O. Daiss

This figure shows the co-authorship network connecting the top 25 collaborators of J.O. Daiss. A scholar is included among the top collaborators of J.O. Daiss based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with J.O. Daiss. J.O. Daiss is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Guerra, Célia Fonseca, Rüdiger Bertermann, D. Troegel, et al.. (2014). Silicon α-Effect: A Systematic Experimental and Computational Study of the Hydrolysis of C_α- and C_γ-Functionalized Alkoxytriorganylsilanes of the Formula Type ROSiMe₂(CH₂)_nX (R = Me, Et;n= 1, 3; X = Functional Group). Organometallics. 33(11). 2721–2737. 30 indexed citations

Hoffmann, Florian, et al.. (2013). Synthesis of 2,2,5,5‐Tetrasubstituted 1,4‐Dioxa‐2,5‐disilacyclohexanes via Organotin(IV)‐Catalyzed Transesterification of (Acetoxymethyl)alkoxysilanes. Chemistry - A European Journal. 19(15). 4818–4825. 5 indexed citations

Barnes, Matthew J., Christian Burschka, Richard Conroy, et al.. (2011). Silicon Analogues of the Nonpeptidic GnRH Antagonist AG‐045572: Syntheses, Crystal Structure Analyses, and Pharmacological Characterization. ChemMedChem. 6(11). 2070–2080. 11 indexed citations

Mizojiri, Ryo, Richard Conroy, J.O. Daiss, et al.. (2010). Large-scale synthesis of 1,1,3,3,6-pentamethyl-1,3-disilaindan-5-ol via a CoBr2/Zn-catalyzed [2+2+2] cycloaddition reaction. Tetrahedron. 66(39). 7738–7742. 6 indexed citations

Tacke, Reinhold, Volker Müller, Rüdiger Bertermann, et al.. (2009). Synthesis and Pharmacological Characterization of Disila‐AM80 (Disila‐tamibarotene) and Disila‐AM580, Silicon Analogues of the RARα‐Selective Retinoid Agonists AM80 (Tamibarotene) and AM580. ChemMedChem. 4(11). 1797–1802. 26 indexed citations

Burschka, Christian, et al.. (2009). Asymmetric Synthesis of the Nonproteinogenic Silicon-Containing α-Amino Acids (R)- and (S)-α-[(Trimethylsilyl)methyl]alanine§Dedicated to Professor Johann Weis on the occasion of his 65th birthday.. Organometallics. 28(20). 6059–6066. 11 indexed citations

Warneck, J.B.H., Matthew J. Barnes, John Mills, et al.. (2008). Action of (R)-sila-venlafaxine and reboxetine to antagonize cisplatin-induced acute and delayed emesis in the ferret. Toxicology and Applied Pharmacology. 232(3). 369–375. 19 indexed citations

Burschka, Christian, J.O. Daiss, Diana Ivanova, et al.. (2007). Silicon Analogues of the Retinoid Agonists TTNPB and 3‐Methyl‐TTNPB, Disila‐TTNPB and Disila‐3‐methyl‐TTNPB: Chemistry and Biology. ChemBioChem. 8(14). 1688–1699. 32 indexed citations

Daiss, J.O., et al.. (2007). The 2,4,6-Trimethoxyphenyl Unit as a Unique Protecting Group for Silicon in Synthesis and the Silylation Potential of (2,4,6-Trimethoxyphenyl)silanes. Organometallics. 26(24). 6014–6028. 17 indexed citations

10.

Showell, Graham A., Matthew J. Barnes, J.O. Daiss, et al.. (2006). (R)-Sila-venlafaxine: A selective noradrenaline reuptake inhibitor for the treatment of emesis. Bioorganic & Medicinal Chemistry Letters. 16(9). 2555–2558. 45 indexed citations

11.

Daiss, J.O., Christian Burschka, John Mills, et al.. (2006). Synthesis, crystal structure analysis, and pharmacological characterization of desmethoxy-sila-venlafaxine, a derivative of the serotonin/noradrenaline reuptake inhibitor sila-venlafaxine. Journal of Organometallic Chemistry. 691(17). 3589–3595. 5 indexed citations

12.

Daiss, J.O., Christian Burschka, John Mills, et al.. (2006). Sila-venlafaxine, a Sila-Analogue of the Serotonin/Noradrenaline Reuptake Inhibitor Venlafaxine: Synthesis, Crystal Structure Analysis, and Pharmacological Characterization. Organometallics. 25(5). 1188–1198. 73 indexed citations

13.

Daiss, J.O., Christian Burschka, John Mills, et al.. (2005). Synthesis, Crystal Structure Analysis, and Pharmacological Characterization of Disila-bexarotene, a Disila-Analogue of the RXR-Selective Retinoid Agonist Bexarotene. Organometallics. 24(13). 3192–3199. 44 indexed citations

14.

Daiss, J.O., Christian Burschka, & Reinhold Tacke. (2004). β-Carbonylsilanes with a silacyclohexane skeleton and additional C-functionalized organyl groups at the silicon atom: synthesis, reactivity, and NMR-spectroscopic characterization. Journal of Organometallic Chemistry. 690(3). 678–684. 2 indexed citations

15.

Daiss, J.O., M. Penka, Christian Burschka, & Reinhold Tacke. (2004). The Si-2,4,6-Trimethoxyphenyl Moiety as a Novel Protecting Group in Organosilicon Chemistry: Alternative Synthesis of rac-Sila-venlafaxine. Organometallics. 23(21). 4987–4994. 24 indexed citations

16.

Daiss, J.O., et al.. (2004). Synthesis of the Multifunctional (Chloromethyl)silanes Cl₂Si(CH₂Cl)₂, (MeO)₂Si(CH₂Cl)₂, RSi(CH₂Cl)₃ (R = 2,4,6-Trimethoxyphenyl), ClSi(CH₂Cl)₃, MeOSi(CH₂Cl)₃, Si(CH₂Cl)₄, and ClCH₂CH₂Si(CH₂Cl)₃. Organometallics. 23(22). 5193–5197. 25 indexed citations

17.

Daiss, J.O., et al.. (2004). A Novel Silicon-Based Uncharged Allosteric Modulator for Ligand Binding to Muscarinic M₂ Receptors: Synthesis and Pharmacological Characterization. Organometallics. 23(25). 6052–6057. 2 indexed citations

18.

Daiss, J.O., et al.. (2003). Synthesis and pharmacological characterization of new silicon-based W84-type allosteric modulators for ligand binding to muscarinic M2 receptors. Journal of Organometallic Chemistry. 686(1-2). 75–83. 10 indexed citations

19.

Schmid, Thomas, et al.. (2003). Enantiopure Chiral Derivatives of the Fragrance Materials Majantol and Sila-majantol: A Bioisosteric Carbon/Silicon Switch with Drastic Effects on the Sensory Characteristics. Organometallics. 22(21). 4343–4346. 27 indexed citations

20.

Daiss, J.O., et al.. (2002). N⁺/Si Replacement as a Tool for Probing the Pharmacophore of Allosteric Modulators of Muscarinic M₂ Receptors: Synthesis, Allosteric Potency, and Positive Cooperativity of Silicon-Based W84 Derivatives. Organometallics. 21(5). 803–811. 17 indexed citations

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