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DC Field | Value | Language |
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dc.contributor.advisor | ||
dc.contributor.author | VIDADALA, SRINIVASA RAO | en_US |
dc.contributor.author | Pimpalpalle, Tukaram M. | en_US |
dc.contributor.author | Linker, Torsten | en_US |
dc.contributor.author | HOTHA, SRINIVAS | en_US |
dc.date.accessioned | 2019-02-14T05:49:14Z | |
dc.date.available | 2019-02-14T05:49:14Z | |
dc.date.issued | 2011-04 | en_US |
dc.identifier.citation | European Journal of Organic Chemistry, .2011(3), 2426-2430. | en_US |
dc.identifier.issn | 1434-193X | en_US |
dc.identifier.issn | 1099-0690 | en_US |
dc.identifier.uri | http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1759 | - |
dc.identifier.uri | https://doi.org/10.1002/ejoc.201100134 | en_US |
dc.description.abstract | 2‐C‐branched methyl glycosides react with various alcohols under gold catalysis to transglycosylated products. The method is applicable for the convenient synthesis of disaccharides. Without nucleophile a selective anomerization occurs, giving first access to α‐configured 2‐C‐nitromethyl glycosides. The results are interesting for the mechanism of gold‐catalyzed glycosidations. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Wiley | en_US |
dc.subject | Gold-catalyzed glycosidations | en_US |
dc.subject | 2-C-nitromethyl?containing glycosides | en_US |
dc.subject | TLC | en_US |
dc.subject | AuBr3-Mediated Transglycosylations | en_US |
dc.subject | 2011 | en_US |
dc.title | Gold‐Catalyzed Reactions of 2‐C‐Branched Carbohydrates: Mild Glycosidations and Selective Anomerizations | en_US |
dc.type | Article | en_US |
dc.contributor.department | Dept. of Chemistry | en_US |
dc.identifier.sourcetitle | European Journal of Organic Chemistry | en_US |
dc.publication.originofpublisher | Foreign | en_US |
Appears in Collections: | JOURNAL ARTICLES |
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