首页> 外文期刊>Chinese Journal of Chemistry >1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU) Catalyzed Regiospecific and Diastereoselective Reaction of Chiral N-(tert-Butanesulfinyl)ketimines and ,β-Unsaturated Trifluoromethyl Ketones
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1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU) Catalyzed Regiospecific and Diastereoselective Reaction of Chiral N-(tert-Butanesulfinyl)ketimines and ,β-Unsaturated Trifluoromethyl Ketones

机译:1,8-二氮杂双环[5.4.0]十一碳-7-烯(DBU)催化手性N-(叔丁烷亚磺酰基)酮亚胺与,β-不饱和三氟甲基酮的区域选择性和非对映选择性反应

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摘要

The reaction of chiral N-(tert-butanesulfinyl)ketimines and ,β-unsaturated trifluoromethyl ketones catalyzed by DBU was achieved under mild conditions. 1,2-Addition products, precursors of chiral trifluoromethylated 1,3-amino alcohols, were obtained diastereoselectively (dr value up to 95:5) in moderate yields (up to 76%). A possible catalytic cycle was proposed.
机译:DBU催化的手性N-(叔丁烷亚磺酰基)酮亚胺与,β-不饱和三氟甲基酮的反应在温和条件下完成。 1,2-加成产物,手性三氟甲基化1,3-氨基醇的前体,以中等收率(高达76%)非对映选择性地获得(dr值高达95:5)。提出了可能的催化循环。

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