Enantioselective and Regiodivergent Addition of Purines to Terminal Allenes: Synthesis of Abacavir

被引:61
|
作者
Thieme, Niels [1 ]
Breit, Bernhard [1 ]
机构
[1] Albert Ludwigs Univ, Inst Organ Chem & Biochem, Alberstr 21, D-79104 Freiburg, Germany
关键词
abacavir; allenes; asymmetric catalysis; carbanucleoside; rhodium; RHODIUM-CATALYZED ADDITION; CARBOCYCLIC NUCLEOSIDE ANALOGS; L-CYCLOPENTENONE DERIVATIVES; ASYMMETRIC-SYNTHESIS; CARBOXYLIC-ACIDS; PRACTICAL SYNTHESIS; CLOSING METATHESIS; ALLYLIC ALKYLATION; ALKYNES; HYDROAMINATION;
D O I
10.1002/anie.201610876
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The rhodium-catalyzed atom-economic asymmetric N-selective intermolecular addition of purine derivatives to terminal allenes is reported. Branched allylic purines were obtained in high yields, regioselectivity and outstanding enantioselectivity utilizing a Rh/Josiphos catalyst. Conversely, linear selective allylation of purines could be realized in good to excellent regio- and E/Z-selectivity with a Pd/dppf catalyst system. Furthermore, the new methodology was applied to a straightforward asymmetric synthesis of carbocyclic nucleoside abacavir.
引用
收藏
页码:1520 / 1524
页数:5
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