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- W1623408013 abstract "Zinc chloride catalyzed reactions of chiral piperazine derivatives 4a–d with 1-alkynes and aldehydes give chiral propargylamines in 67–95 % yields with up to 99:1 dr. The chiral propargylamines are converted into chiral allenes by using zinc bromide in short reaction times (1–2 h) in high enantioselectivities (up to 99 % ee) in good yields (up to 89 %). The chiral piperazines are recovered in good yields (79–86 %) by reduction of the imine byproducts in situ by using NaBH4. Unexpectedly, the chiral aryl-substituted allenes undergo facile cyclodimerization under neat conditions at 25 °C, in contrast to an earlier report that cyclodimerization takes place at 80 °C in benzene, which further illustrates the importance of the two-step procedure reported herein because the chiral propargylamine may be converted into chiral allene when required." @default.
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- W1623408013 date "2014-08-06" @default.
- W1623408013 modified "2023-09-27" @default.
- W1623408013 title "Zinc Salt Promoted Diastereoselective Synthesis of Chiral Propargylamines Using Chiral Piperazines and Their Enantioselective Conversion into Chiral Allenes" @default.
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- W1623408013 doi "https://doi.org/10.1002/ejoc.201402766" @default.
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