Selective Deoxygenation of Allylic Alcohol: Stereocontrolled Synthesis of Lavandulol
Author:
Affiliation:
1. Department of Chemistry, Department of Nano Science and Engineering, Myong Ji University, Yongin, Kyunggi-Do, 449-728, Korea
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol200779y
Reference19 articles.
1. Identification and synthesis of the sex pheromone of the vine mealybug, Planococcus ficus
2. General chiral route to irregular monoterpenes via a common intermediate: syntheses of (S)-lavandulol, cis(1S,3R)-chrysanthemol, (1R,2S)-rothrockene, and (R)-santolinatriene
3. Regio- and Stereoselective Synthesis of Allylic and Homoallylic Alcohols by the Reductive Desulfonylation of Allylic Sulfone Derivatives. Application to the Syntheses of (±)-Lavandulol and Isolavandulol
4. Highly efficient terpenoid pheromone syntheses via regio- and stereocontrolled processing of allyllithiums generated by reductive lithiation of allyl phenyl thioethers
5. Synthesis of (±)-lavandulol and its related homoallylic alcohol via allyl transfer from sulphur to tin
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