![Chemistry / Organic reactions / Catalysis / Hydrogenation / Hydrogen / Organic chemistry / Organocatalysis / Enamine / Strecker amino acid synthesis / Max Planck Institute for Coal Research / Asymmetric hydrogenation / Enantioselective synthesis Chemistry / Organic reactions / Catalysis / Hydrogenation / Hydrogen / Organic chemistry / Organocatalysis / Enamine / Strecker amino acid synthesis / Max Planck Institute for Coal Research / Asymmetric hydrogenation / Enantioselective synthesis](https://www.pdfsearch.io/img/b6709c2e4e24475f065a50f0689c1e4e.jpg) Date: 2016-08-08 05:21:02Chemistry Organic reactions Catalysis Hydrogenation Hydrogen Organic chemistry Organocatalysis Enamine Strecker amino acid synthesis Max Planck Institute for Coal Research Asymmetric hydrogenation Enantioselective synthesis | | Sayantani Das, Luping Liu, Yiying Zheng, M. Wasim Alachraf, Walter Thiel*, Chandra Kanta De* and Benjamin List*: Nitrated Confined Imidodiphosphates Enable a Catalytic Asymmetric Oxa-Pictet–Spengler Reaction Add to Reading ListSource URL: www.kofo.mpg.deDownload Document from Source Website File Size: 202,96 KBShare Document on Facebook
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