Division of Chemistry and Biochemistry, Graduate School of Natural Science and Technology, Okayama University, Okayama 700-8530, Japan.
Chem Commun (Camb). 2010 Dec 7;46(45):8624-6. doi: 10.1039/c0cc03706k. Epub 2010 Oct 12.
α,α,α-Trifluoroacetophenone (2), which is susceptible to noncatalytic reduction by BH(3), could be reduced to chiral alcohol up to 90% ee by using electronically tuned-CBS catalyst (1) with BH(3). The enantioselectivities highly correlated with the differential orbital energies between 1-BH(3) adduct and 2, which were calculated by DFT method.
三氟乙酰苯(2)易被 BH(3)非催化还原,用经电子调谐的 CBS 催化剂(1)与 BH(3)还原可高达 90%ee 得到手性醇。对映选择性与 1-BH(3)加合物和 2 之间的差分轨道能密切相关,这些轨道能通过 DFT 方法计算得出。