Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous Abstract"Exposure to volatile organic compounds and health risks among residents in an area affected by a petrochemical complex in Rayong, Thailand"    Next AbstractHybrid Photonic Cavity with Metal-Organic Framework Coatings for the Ultra-Sensitive Detection of Volatile Organic Compounds with High Immunity to Humidity »

Enantiomer


Title:CCL- and PLE-catalyzed reverse enantiomeric separation of various (+/-)-2-thienylcarbinols
Author(s):Tanyeli C; Akhmedov IM; Ozdemirhan D;
Address:"Department of Chemistry, Middle East Technical University, Ankara, Turkey. tanyeli@metu.edu.tr"
Journal Title:Enantiomer
Year:2001
Volume:6
Issue:5
Page Number:259 - 265
DOI:
ISSN/ISBN:1024-2430 (Print) 1024-2430 (Linking)
Abstract:"(+/-)-2-Thienylcarbinols and their O-acetyl derivatives were resolved in reverse separation by CCL and PLE catalysed hydrolysis to afford optically active 2-thienylcarbinols in 35%-99% e.e. that are valuable chiral building blocks, in particular in the synthesis of pheromones and some alkoloid type natural products. Absolute configurations were determined by the correlation of specific rotation values with the literature and by transforming into the corresponding secondary alcohols via reductive desulfurization by Ra-Ni"
Keywords:
Notes:"PubMed-not-MEDLINETanyeli, C Akhmedov, I M Ozdemirhan, D eng 2002/01/05 Enantiomer. 2001; 6(5):259-65"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 22-11-2024