催化作用
试剂
对映选择合成
组合化学
胺气处理
化学
基质(水族馆)
咬合
有机化学
计算机科学
生物
生态学
计算机图形学(图像)
作者
Michael U. Luescher,Jeffrey W. Bode
标识
DOI:10.1002/anie.201505167
摘要
Abstract Commercially available SnAP (stannyl amine protocol) reagents allow the transformation of aldehydes and ketones into a variety of N‐unprotected heterocycles. By identifying new ligands and reaction conditions, a robust catalytic variant that expands the substrate scope to previously inaccessible heteroaromatic substrates and new substitution patterns was realized. It also establishes the basis for a catalytic enantioselective process through the use of chiral ligands.
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