Silylmethylene radical cyclization. A stereoselective approach to branched sugars
Article Properties
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LanguageEnglish
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DOI (url)
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Publication Date1993/06/01
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Journal
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Indian UGC (journal)
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Refrences54
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Citations25
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Valérie Pedretti
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Jean-Maurice Mallet
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Pierre Sinaÿ
Cite
Pedretti, Valérie, et al. “Silylmethylene Radical Cyclization. A Stereoselective Approach to Branched Sugars”. Carbohydrate Research, vol. 244, no. 2, 1993, pp. 247-5, https://doi.org/10.1016/0008-6215(83)85005-8.
Pedretti, V., Mallet, J.-M., & Sinaÿ, P. (1993). Silylmethylene radical cyclization. A stereoselective approach to branched sugars. Carbohydrate Research, 244(2), 247-257. https://doi.org/10.1016/0008-6215(83)85005-8
Pedretti, Valérie, Jean-Maurice Mallet, and Pierre Sinaÿ. “Silylmethylene Radical Cyclization. A Stereoselective Approach to Branched Sugars”. Carbohydrate Research 244, no. 2 (1993): 247-57. https://doi.org/10.1016/0008-6215(83)85005-8.
Pedretti V, Mallet JM, Sinaÿ P. Silylmethylene radical cyclization. A stereoselective approach to branched sugars. Carbohydrate Research. 1993;244(2):247-5.
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Refrences
| Title | Journal | Journal Categories | Citations | Publication Date |
|---|---|---|---|---|
| Preferred conformation of C-glycosides. 7. Preferred conformation of carbon analogs of isomaltose and gentiobiose | The Journal of Organic Chemistry |
| 42 | 1991 |
| Preferred conformation of C-glycosides. 6. Conformational similarity of glycosides and corresponding C-glycosides | The Journal of Organic Chemistry |
| 33 | 1991 |
| Synthesis of Methylene Bridged C-Disaccharides | Journal of Carbohydrate Chemistry |
| 18 | 1991 |
| A New Approach for theC-Alkylation of Unsaturated Sugars Involving the Benzothiazol-2-Ylthio Leaving Group | Journal of Carbohydrate Chemistry |
| 5 | 1990 |
| A facile conversion of 3,4-O-isopropylidene-β-d-galactopyranosides into 4-deoxy-α-l-threo-hex-4-enopyranoside and l-arabino-hexos-5-ulose derivatives | Carbohydrate Research |
| 17 | 1989 |
Refrences Analysis
The category
Science: Chemistry 25
is the most frequently represented among the references in this article. It primarily includes studies from Journal of the American Chemical Society and Journal of the Chemical Society, Chemical Communications. The chart below illustrates the number of referenced publications per year.
Refrences used by this article by year
Citations
| Title | Journal | Journal Categories | Citations | Publication Date |
|---|---|---|---|---|
Silylated Sugars – Synthesis and Properties | Synlett |
| 1 | 2021 |
Reactivity, Selectivity, and Synthesis of 4‐C‐Silylated Glycosyl Donors and 4‐Deoxy Analogues | Angewandte Chemie | 4 | 2020 | |
| Reactivity, Selectivity, and Synthesis of 4‐C‐Silylated Glycosyl Donors and 4‐Deoxy Analogues | Angewandte Chemie International Edition |
| 9 | 2020 |
| Synthesis of l-Pyranosides by Hydroboration of Hex-5-enopyranosides Revisited | The Journal of Organic Chemistry |
| 9 | 2016 |
| Efficient functionalizations of a pyranosido-pyrimidine scaffold | Tetrahedron |
| 5 | 2009 |
Citations Analysis
The category
Science: Chemistry 18
is the most commonly referenced area in studies that cite this article. The first research to cite this article was titled Exclusive 6-endo radical cyclizations of α-silyl radicals derived from carbohydrate allylic silylethers and was published in 1994. The most recent citation comes from a 2021 study titled Silylated Sugars – Synthesis and Properties. This article reached its peak citation in 2005, with 3 citations. It has been cited in 13 different journals. Among related journals, the Tetrahedron cited this research the most, with 6 citations. The chart below illustrates the annual citation trends for this article.