A Topochemically Controlled, Regiospecific Fullerene Bisfunctionalization
Article Properties
-
LanguageEnglish
-
DOI (url)
-
Publication Date1996/06/17
-
Indian UGC (journal)
-
Refrences29
-
Citations79
-
Bernhard Kräutler
-
Thomas Müller
-
Joseph Maynollo
-
Karl Gruber
-
Christoph Kratky
-
Philippe Ochsenbein
-
Dieter Schwarzenbach
-
Hans‐Beat Bürgi
Cite
Kräutler, Bernhard, et al. “A Topochemically Controlled, Regiospecific Fullerene Bisfunctionalization”. Angewandte Chemie International Edition in English, vol. 35, no. 11, 1996, pp. 1204-6, https://doi.org/10.1002/anie.199612041.
Kräutler, B., Müller, T., Maynollo, J., Gruber, K., Kratky, C., Ochsenbein, P., Schwarzenbach, D., & Bürgi, H. (1996). A Topochemically Controlled, Regiospecific Fullerene Bisfunctionalization. Angewandte Chemie International Edition in English, 35(11), 1204-1206. https://doi.org/10.1002/anie.199612041
Kräutler, Bernhard, Thomas Müller, Joseph Maynollo, Karl Gruber, Christoph Kratky, Philippe Ochsenbein, Dieter Schwarzenbach, and Hans‐Beat Bürgi. “A Topochemically Controlled, Regiospecific Fullerene Bisfunctionalization”. Angewandte Chemie International Edition in English 35, no. 11 (1996): 1204-6. https://doi.org/10.1002/anie.199612041.
Kräutler B, Müller T, Maynollo J, Gruber K, Kratky C, Ochsenbein P, et al. A Topochemically Controlled, Regiospecific Fullerene Bisfunctionalization. Angewandte Chemie International Edition in English. 1996;35(11):1204-6.
Refrences
| Title | Journal | Journal Categories | Citations | Publication Date |
|---|---|---|---|---|
| 10.1039/C39930001296 | ||||
| Synthesis, purification, and characterization of the 1 : 1 addition product of C60 and anthracene | Journal of the Chemical Society, Chemical Communications | 80 | 1993 | |
| Crystal Engineering–The Design of Organic Solids | 1989 | |||
| Organic Solid State Chemistry | 1987 | |||
| A Highly Symmetric Sixfold Cycloaddition Product of Fullerene C60 | Angewandte Chemie International Edition in English | 62 | 1995 |
Citations
| Title | Journal | Journal Categories | Citations | Publication Date |
|---|---|---|---|---|
Host‐Guest Chemistry in Binary and Ternary Complexes Utilizing π‐Conjugated Carbon Nanorings | ChemPlusChem |
| 5 | 2024 |
Recent advances in supramolecular fullerene chemistry | Chemical Society Reviews |
| 2024 | |
| A multiscale ONIOM study of the buckminsterfullerene (C60) Diels–Alder reaction: from model design to reaction path analysis | Journal of Molecular Modeling |
| 2022 | |
| Regioselective access to orthogonal Diels-Alder C60 bis-adducts and tris-heteroadducts via supramolecular mask strategy | Cell Reports Physical Science | 8 | 2022 | |
| Successive Diels–Alder Cycloadditions of Cyclopentadiene to [10]CPP⊃C60: A Computational Study | The Journal of Organic Chemistry |
| 6 | 2022 |
Citations Analysis
The category
Science: Chemistry 69
is the most commonly referenced area in studies that cite this article. The first research to cite this article was titled Crystal engineering: solid state supramolecular synthesis and was published in 1997. The most recent citation comes from a 2024 study titled Host‐Guest Chemistry in Binary and Ternary Complexes Utilizing π‐Conjugated Carbon Nanorings. This article reached its peak citation in 1997, with 8 citations. It has been cited in 41 different journals, 2% of which are open access. Among related journals, the Journal of the American Chemical Society cited this research the most, with 6 citations. The chart below illustrates the annual citation trends for this article.