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Pyrrole‐Protected β‐Aminoalkylzinc Reagents for the Enantioselective Synthesis of Amino‐Derivatives

Chiral β‐aminoalkylzinc halides were prepared starting from optically pure commercial β‐amino‐alcohols. These amino‐alcohols were converted to the corresponding N‐pyrrolyl‐protected alkyl iodides which undergo a zinc insertion in the presence of LiCl (THF, 25 °C, 10–90 min). Subsequent Negishi cross...

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書目詳細資料
發表在:Chemistry
Main Authors: Leroux, Marcel, Huang, Wan‐Yun, Lemke, Yannick, Koller, Thaddäus J., Karaghiosoff, Konstantin, Knochel, Paul
格式: Artigo
語言:Inglês
出版: John Wiley and Sons Inc. 2020
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC7497206/
https://ncbi.nlm.nih.gov/pubmed/32196786
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/chem.202000870
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