DOI | Resolve DOI: https://doi.org/10.1039/c3cc48963a |
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Author | Search for: Ma, X.; Search for: Zhang, J.; Search for: Tang, Q.; Search for: Ke, J.; Search for: Zou, W.1; Search for: Shao, H. |
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Affiliation | - National Research Council of Canada. NRC Institute for Biological Sciences
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Format | Text, Article |
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Subject | carbohydrate derivative; cyclopropane derivative; furo[2,3 b]furan derivative; ketone derivative; pyran derivative; tin chloride; catalysis; chirality; cycloaddition; quantum yield; reaction analysis; stereochemistry; synthesis |
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Abstract | Stereospecific [3+2] cycloaddition of 1,2-cyclopropanated sugars and ketones catalyzed by SnCl4 is described. The method offers multi-substituted perhydrofuro[2,3-b]furans (bis-THFs) and perhydrofuro[2,3-b] pyrans containing a quaternary carbon chiral center in good to excellent yields. © 2014 The Royal Society of Chemistry. |
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Publication date | 2014 |
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In | |
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Language | English |
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Peer reviewed | Yes |
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NPARC number | 21272121 |
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Export citation | Export as RIS |
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Report a correction | Report a correction (opens in a new tab) |
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Record identifier | 378c7f56-4ff8-497f-832d-3a8e1593482d |
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Record created | 2014-07-23 |
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Record modified | 2020-04-22 |
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