English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

and Dong Jun KimDepartmet of Chemistry, Hallym University, Chunchon 200-702, KoreaReceived June 7, 2004A general route for the synthesis of optically active unhindered aliphatic alcohols, where the steric demandsbetween two alkyl groups adjacent to the carbinol are similar, with high enantiomeric purity has beendeveloped by sulfoxifation of chiral β-hydroxy sulfides, followed by alkylation and desulfurization.Key Words : Chiral aliphatic alcohols, Asymmetric reduction, (S)-CBS oxazaborolidine, Chiral β-hydroxysulfidesIntroductionSome optically active unhindered secondary aliphaticalcohols are extremely important as naturally occurringbiologically active substances. For examples, optically active3-octanol,

A Convenient Synthesis of Optically Active Unhindered Aliphatic Alcohols with High Optical Purity from Non-Racemic β-Hydroxy Sulfides