Autor: |
Toru Imai, Tomohiro Michitaka, Akihito Hashidzume |
Jazyk: |
angličtina |
Rok vydání: |
2016 |
Předmět: |
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Zdroj: |
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 2668-2672 (2016) |
Druh dokumentu: |
article |
ISSN: |
1860-5397 |
DOI: |
10.3762/bjoc.12.263 |
Popis: |
Formose reactions were carried out in the presence of low molecular weight and macromolecular boronic acid compounds, i.e., sodium phenylboronate (SPB) and a copolymer of sodium 4-vinylphenylboronate with sodium 4-styrenesulfonate (pVPB/NaSS), respectively. The boronic acid compounds provided different selectivities; sugars of a small carbon number were formed favorably in the presence of SPB, whereas sugar alcohols of a larger carbon number were formed preferably in the presence of pVPB/NaSS. |
Databáze: |
Directory of Open Access Journals |
Externí odkaz: |
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