Graduate School of Natural Science and Technology, Kanazawa University , Kakuma-machi, Kanazawa 920-1192, Japan.
Faculty of Chemistry and Chemical Technology, University of Ljubljana , Večna pot 113, SI-1000, Ljubljana, Slovenia.
Org Lett. 2016 Aug 19;18(16):4036-9. doi: 10.1021/acs.orglett.6b01894. Epub 2016 Aug 2.
An investigation of the recently reported "fully catalytic Mitsunobu reaction" using catalytic amounts of a phosphine reagent and an azo reagent has shown that although benzyl 4-nitrobenzoate is formed under the fully catalytic conditions, the same result is obtained if the hydrazine catalyst is omitted, indicating that this is not a Mitsunobu reaction. In addition, when the reaction between (-)-ethyl lactate and 4-nitrobenzoic acid was carried out using the "fully catalytic" method, the corresponding ester was formed but in very low yield and with predominant retention of configuration. Unfortunately, the system catalytic in phosphine reagent is incompatible with that in the azo reagent.
对最近报道的“完全催化 Mitsunobu 反应”使用催化量的膦试剂和偶氮试剂进行了研究,结果表明,尽管在完全催化条件下形成了苄基 4-硝基苯甲酸酯,但如果省略肼催化剂,也会得到相同的结果,这表明这不是 Mitsunobu 反应。此外,当使用“完全催化”方法进行(-)-乳酸乙酯与 4-硝基苯甲酸的反应时,形成了相应的酯,但产率很低,且构型主要保留。不幸的是,在膦试剂中催化的体系与偶氮试剂中的体系不兼容。