The first synthesis of geranyllinalool enantiomers

Svatos, A.; Urbanova, K.; Valterova, I.

doi:10.1135/cccc20020083

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The first synthesis of geranyllinalool enantiomers

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Svatos, A.
Research Group Mass Spectrometry, MPI for Chemical Ecology, Max Planck Society;

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Svatos, A., Urbanova, K., & Valterova, I. (2002). The first synthesis of geranyllinalool enantiomers. Collection of Czechoslovak Chemical Communications, 67(1), 83-90. doi:10.1135/cccc20020083.

Cite as: https://hdl.handle.net/11858/00-001M-0000-0012-B3C3-5

Abstract

(3R)-(-)-Geranyllinalool and its (3S)-(+)-isomer were synthesized in 7 steps starting from both enantiomers of citramalic acid and geranyl bromide. The synthetic sequence established the absolute configurations of naturally occurring geranyllinalools fo