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Epoxy Alcohols (epoxy + alcohol)

Distribution by Scientific Domains
Chemistry100%

Selected Abstracts

Concise Synthesis of 2,6-Disubstituted Morpholines by Cyclization of Epoxy Alcohols

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 13 2007
Domenico Albanese
Abstract A novel, straightforward and high yielding synthesis of enantiomerically pure 2,6-disubstituted morpholines was developed by acid-catalyzed cyclization of epoxy alcohols. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007) [source]

Highly Enantio- and Diastereoselective One-Pot Synthesis of Acyclic Epoxy Alcohols and Allylic Epoxy Alcohols.

CHEMINFORM, Issue 7 2006
Ann Rowley Kelly
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access the actual ChemInform Abstract, please click on HTML or PDF. [source]

Concerning the Efficient Conversion of Epoxy Alcohols into Epoxy Ketones Using Dioxiranes.

CHEMINFORM, Issue 16 2005
Lucia D'Accolti
Abstract For Abstract see ChemInform Abstract in Full Text. [source]

ChemInform Abstract: Regioselective Alkyl and Alkynyl Substitution Reactions of Epoxy Alcohols by the Use of Organoaluminum Ate Complexes: Regiochemical Reversal of Nucleophilic Substitution Reactions.

CHEMINFORM, Issue 39 2001
Minoru Sasaki
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source]

Synthesis of all Four Stereoisomers of Leucomalure, Components of the Female Sex Pheromone of the Satin Moth, Leucoma salicis

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 7 2003
Shin-etsu Muto
Abstract Lipase PS-C(Amano)-catalyzed asymmetric acetylation of (±)-4-(tert -butyldiphenylsilyloxy)- cis -2,3-epoxy-1-butanol afforded the (2R,3S)-epoxy alcohol and the (2S,3R)-epoxyacetate, which were converted into all of the four stereoisomers of leucomalure [(3Z)- cis -6,7- cis -9,10-diepoxy-3-henicosene], the female sex pheromone of the Satin moth, Leucoma salicis. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003) [source]

Synthesis of Murisolin, (15R, 16R, 19R, 20S)-Murisolin,A, and (15R, 16R, 19S, 20S)-16,19- cis -Murisolin and Their Inhibitory Action with Bovine Heart Mitochondrial Complex,I

CHEMISTRY - AN ASIAN JOURNAL, Issue 6 2006
Yasunao Hattori
Abstract The asymmetric total synthesis of murisolin, (15R, 16R, 19R, 20S)-murisolin,A, and (15R, 16R, 19S, 20S)-16,19- cis -murisolin was performed by using an epoxy alcohol as a versatile chiral building block for synthesizing the stereoisomers of mono-THF annonaceous acetogenins. The inhibitory activity of these murisolin compounds was examined with bovine heart mitochondrial complex,I, and they showed almost the same activity. [source]