期刊
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2007, 期 6, 页码 891-897出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.200600643
关键词
trifluoromethylation; asymmetric synthesis; enantioselectivity; diastereoselectivity
The importance of trifluoromethylated molecules has undergone regular growth during the last years, and asymmetric molecules with the CF3 group borne by a chiral carbon have become more popular. However, methods used to achieve such molecules are still limited. The building block strategy has been the method most employed these last years and stereocontrolled trifluoromethylation reactions have begun to emerge as potential valuable alternatives. Trifluoromethylation of chiral molecules, by using diastereoselective induction, seems promising and already gives good results in certain cases. However, although actively studied to this day, the enantioselective trifluoromethylation of prochiral compounds is still not very efficient even if some interesting results have been already described. Nevertheless, such reactions still present a challenge in terms of efficiency. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007).
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