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Chiral Bicyclic Bridgehead Phosphoramidite (Briphos) Ligands for Asymmetric Rhodium-Catalyzed 1,2- and 1,4-Addition
The Journal of Organic Chemistry ( IF 3.3 ) Pub Date : 2016-04-25 00:00:00 , DOI: 10.1021/acs.joc.6b00033
Ansoo Lee 1 , Hyunwoo Kim 1
Affiliation  

A complementary solution for Rh-catalyzed enantioselective 1,2- and 1,4-arylation with two structurally related chiral ligands is reported. A chiral bicyclic bridgehead phosphoramidite (briphos) ligand derived from 1-aminoindane was efficient for the 1,2-arylation of N-sulfonyl imines, while that derived from 1,2,3,4-tetrahydro-1-naphthylamine was efficient for 1,4-arylation of α,β-unsaturated cyclic ketones. For α,β-unsaturated N-tosyl ketimines, the briphos derived from 1-aminoindane was found to selectively provide γ,γ-diaryl N-tosyl enamines with high yields and stereoselectivities.

中文翻译:

手性双环桥头亚磷酰胺(Briphos)配体,用于不对称铑催化的1,2-和1,4-加成

报道了具有两个结构上相关的手性配体的Rh催化对映选择性1,2-和1,4-芳基化的互补溶液。衍生自1-氨基茚满的手性双环桥头亚磷酰胺(briphos)配体对于N-磺酰基亚胺的1,2-芳基化反应有效,而衍生自1,2,3,4-四氢-1-萘胺的手性双环桥头磷酰胺则有效α,β-不饱和环酮的; 4-芳基化。对于α,β-不饱和N-甲苯磺酰基酮亚胺,发现衍生自1-氨基茚满的Briphos选择性地提供了高产率和立体选择性的γ,γ-二芳基N-甲苯磺酰基烯胺。
更新日期:2016-04-25
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