The Dual Roles of Oxodiperoxovanadate Both as a Nucleophile and an Oxidant in the Green Oxidation of Benzyl Alcohols or Benzyl Halides to Aldehydes and Ketones
Correction(s) for this article
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The Dual Roles of Oxodiperoxovanadate Both as a Nucleophile and an Oxidant in the Green Oxidation of Benzyl Alcohols or Benzyl Halides to Aldehydes and Ketones
- Chunbao Li Dr.,
- Pengwu Zheng,
- Jie Li,
- Hang Zhang,
- Yi Cui,
- Qiyun Shao,
- Xiujie Ji,
- Jian Zhang,
- Pengying Zhao,
- Yanli Xu,
- Volume 119Issue 30Angewandte Chemie
- pages: 5744-5744
- First Published online: July 13, 2007
Chunbao Li Dr.
Department of Chemistry, School of Sciences, Tianjin University, Tianjin 300072, China, Fax: (+86) 22-2740-3475
Search for more papers by this authorPengwu Zheng
Department of Chemistry, School of Sciences, Tianjin University, Tianjin 300072, China, Fax: (+86) 22-2740-3475
Search for more papers by this authorJie Li
Department of Chemistry, School of Sciences, Tianjin University, Tianjin 300072, China, Fax: (+86) 22-2740-3475
Search for more papers by this authorHang Zhang
Department of Chemistry, School of Sciences, Tianjin University, Tianjin 300072, China, Fax: (+86) 22-2740-3475
Search for more papers by this authorYi Cui
Department of Chemistry, School of Sciences, Tianjin University, Tianjin 300072, China, Fax: (+86) 22-2740-3475
Search for more papers by this authorQiyun Shao
Department of Chemistry, School of Sciences, Tianjin University, Tianjin 300072, China, Fax: (+86) 22-2740-3475
Search for more papers by this authorXiujie Ji
Department of Chemistry, School of Sciences, Tianjin University, Tianjin 300072, China, Fax: (+86) 22-2740-3475
Search for more papers by this authorJian Zhang
Department of Chemistry, School of Sciences, Tianjin University, Tianjin 300072, China, Fax: (+86) 22-2740-3475
Search for more papers by this authorPengying Zhao
Department of Chemistry, School of Sciences, Tianjin University, Tianjin 300072, China, Fax: (+86) 22-2740-3475
Search for more papers by this authorYanli Xu
Department of Chemistry, School of Sciences, Tianjin University, Tianjin 300072, China, Fax: (+86) 22-2740-3475
Search for more papers by this authorChunbao Li Dr.
Department of Chemistry, School of Sciences, Tianjin University, Tianjin 300072, China, Fax: (+86) 22-2740-3475
Search for more papers by this authorPengwu Zheng
Department of Chemistry, School of Sciences, Tianjin University, Tianjin 300072, China, Fax: (+86) 22-2740-3475
Search for more papers by this authorJie Li
Department of Chemistry, School of Sciences, Tianjin University, Tianjin 300072, China, Fax: (+86) 22-2740-3475
Search for more papers by this authorHang Zhang
Department of Chemistry, School of Sciences, Tianjin University, Tianjin 300072, China, Fax: (+86) 22-2740-3475
Search for more papers by this authorYi Cui
Department of Chemistry, School of Sciences, Tianjin University, Tianjin 300072, China, Fax: (+86) 22-2740-3475
Search for more papers by this authorQiyun Shao
Department of Chemistry, School of Sciences, Tianjin University, Tianjin 300072, China, Fax: (+86) 22-2740-3475
Search for more papers by this authorXiujie Ji
Department of Chemistry, School of Sciences, Tianjin University, Tianjin 300072, China, Fax: (+86) 22-2740-3475
Search for more papers by this authorJian Zhang
Department of Chemistry, School of Sciences, Tianjin University, Tianjin 300072, China, Fax: (+86) 22-2740-3475
Search for more papers by this authorPengying Zhao
Department of Chemistry, School of Sciences, Tianjin University, Tianjin 300072, China, Fax: (+86) 22-2740-3475
Search for more papers by this authorYanli Xu
Department of Chemistry, School of Sciences, Tianjin University, Tianjin 300072, China, Fax: (+86) 22-2740-3475
Search for more papers by this authorGraphical Abstract
Doppelrolle: Oxodiperoxovanadat (VO(O2)2−) reagiert unter sauren Bedingungen als Nucleophil und als Oxidationsmittel für Benzylalkohole und -halogenide. Diese werden mit H2O2 in Wasser mit VO(O2)2− als Katalysator in Gegenwart eines Phasentransferkatalysators (PTC) zu aromatischen Aldehyden und Ketonen umgesetzt (siehe Schema).
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