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Pan Jarglis

Technische Hochschule

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Publication

Featured researches published by Pan Jarglis.

Tetrahedron Letters | 1982

Boron trifluoride-catalyzed oxidation of glycal esters: An effective and mild method for their conversion into α,β-unsaturated lactones☆

Pan Jarglis; Frieder W. Lichtenthaler

An effective, one-step procedure for conversion of glycal and 2-acyloxyglycal esters to 2,3-unsaturated lactones has been developed, involving BF3-induced removal of the allylic acyloxy function and oxidation with m-chloroperbenzoic acid or pyridinium chlorochromate.

Tetrahedron Letters | 1980

Selective deacylation of enol esters with hydroxylamine

Frieder W. Lichtenthaler; Pan Jarglis

Abstract An effective procedure for selectively cleaving enol esters in the presence of normal ester functions has been developed, involving hydroxylaminolysis to the oxime of the parent ketone.

Synthesis | 1988

Convenient One-Pot Conversion of Alcohols into Esters via Hemiacetal Intermediates

Frieder W. Lichtenthaler; Pan Jarglis; Klaus Lorenz

European Journal of Organic Chemistry | 1989

Enantiomerically Pure Building Blocks from Sugars, 9 An Expedient Approach to Pyranoid Ene and Enol Lactones by BF3-Catalyzed Peroxidation of Glycal and Hydroxyglycal Esters

Frieder W. Lichtenthaler; Stephan Rönninger; Pan Jarglis

European Journal of Organic Chemistry | 1983

Sugar enolones, XVIII. ―Stereocontrolled functionalization at proanomeric centres by photobromination: a novel efficient access to oxo- and oximinoglycosyl bromides

Frrieder W. Lichtenthaler; Pan Jarglis; Walter Hempe

Angewandte Chemie | 2006

Eine stereospezifische Synthese von (S,S)‐Palythazin aus D‐Glucose

Pan Jarglis; Frieder W. Lichtenthaler

Carbohydrate Research | 1984

Simple synthesis of (S)-parasorbic acid and other (5S)-hydroxy six-carbon synthons from L-rhamnose☆

Frieder W. Lichtenthaler; Franz D. Klinger; Pan Jarglis

Chemische Berichte | 1980

Sugar enolones, XII. Peroxidation of pyranose‐derived enol esters: An efficacious synthesis of peracetylhexosuloses and their conversion into γ‐pyrones via 3,2‐enolones

Frieder W. Lichtenthaler; Pan Jarglis

Angewandte Chemie | 2006

Funktionalisierung proanomerer Zentren durch Photobromierung: Ein neuer Zugang zu Oxo‐ und Acyloxyimino‐glycosylbromiden

Frieder W. Lichtenthaler; Pan Jarglis

Angewandte Chemie | 1982

Functionalization at Proanomeric Centres by Photobromination. A Novel Access to Oxo‐ and Acyloxyimino‐glycosyl Bromides

Frieder W. Lichtenthaler; Pan Jarglis

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Frieder W. Lichtenthaler

Technische Universität Darmstadt

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Shigeru Nishiyama

Keio University

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Stephan Rönninger

Darmstadt University of Applied Sciences

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Franz D. Klinger

Technische Hochschule

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Frrieder W. Lichtenthaler

Darmstadt University of Applied Sciences

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Klaus Lorenz

Technische Hochschule

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Walter Hempe

Darmstadt University of Applied Sciences

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