对映选择合成
立体中心
催化作用
环加成
布朗斯特德-洛瑞酸碱理论
非对映体
化学
有机化学
反应性(心理学)
四氢呋喃
吡咯
立体化学
组合化学
替代医学
病理
医学
溶剂
作者
Lei Yu,Jordan Diaz,Asja A. Kroeger,Michelle L. Coote,Philip Wai Hong Chan
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2024-08-21
卷期号:14 (17): 13269-13282
被引量:3
标识
DOI:10.1021/acscatal.3c05041
摘要
A chiral Brønsted acid-catalyzed synthetic method that enables the enantioselective formal [2 + 2 + 2] cycloaddition of 3-vinyl-1H-indoles with nitrosobenzenes is described. Through this previously unknown mode of reactivity of the nitrosoarene, the ring formation protocol offers access to a wide variety of fully substituted 1,2-oxazinanes as a single regioisomer. With four stereogenic centers generated in the product, the N,O-heterocycle was also furnished, in most cases, as a single diastereomer in yields of up to 94% and with enantiomeric excess (ee) values of up to 99%. The synthetic utility of the catalytic method was demonstrated by the 2 mmol scale preparation of one example and its further functional group transformations. Included in this is the selective conversion of the 1,2-oxazinane to either its tetrahydrofuran or a partially hydrogenated pyrrole derivative. Experimental and computational studies based on azaphilic and hydrogen-bonding interactions between the two substrates with the chiral phosphoric acid provide insight into the observed product selectivities.
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