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Featured researches published by Erhard Roeder.


Plant Cell Tissue and Organ Culture | 1997

Camptothecin and 10-hydroxycamptothecin in callus and plantlets of t Camptotheca acuminata

Helmut Wiedenfeld; Mirosława Furmanowa; Erhard Roeder; Joanna Guzewska; Wlodzimierz Gustowski

The process of callus induction, organogenesis and plantlets regeneration of Camptotheca acuminata Decne is reported. The highest growth rate of callus was observed on MS medium with 1 mg l−1 NAA, 1 mg l−1 kinetin and 60 g l−1 sucrose. All tissues and organs developed in vitro contain camptothecin and 10-hydroxycamptothecin. The presence of 10-hydroxycamptothecin in shoots and callus of Camptotheca acuminata Decne is reported for the first time. The alkaloids were detected and identified using HPLC methods.


Phytochemistry | 1990

Carbon-13 NMR spectroscopy of pyrrolizidine alkaloids

Erhard Roeder

Abstract 13 C NMR chemical shifts of more than 130 naturally occurring alkaloids published up to 1988 are listed. The utility of 13 C NMR spectroscopy for the structure elucidation of these compounds combined with mass spectra is discussed.


Phytochemistry | 1991

Pyrrolizidine alkaloids of Heliotropium spathulatum

Erhard Roeder; Eberhard Breitmaier; Helena Birecka; Michael W. Frohlicht; Andrea Badzies-Crombach

Abstract Isolation and structural determination of the pyrrolizidine alkaloids of Heliotropium spathulatum are reported. The alkaloids lycopsamine, amabiline, curassavinine, coromandalinine, heliovicine, coromandaline, curassavine and the two new pyrrolizidine alkaloids, heliospathine and heliospathuline were determined by spectroscopic methods. Traces of another new alkaloid were detected.


Phytochemistry | 1991

Pyrrolizidine alkaloids from Echium pininana

Erhard Roeder; K. Liu; T. Bourauel

Abstract Seven pyrrolizidine alkaloids were isolated from Echium pininana and their structures determined by spectroscopic methods. One of them is new and the name echiupinine is proposed for it. The corresponding echiupinine-N-oxide and the previously undescribed myoscorpine-N-oxide are also present in this plant species.


Phytochemistry | 1991

Pyrrolizidine alkaloids from Senecio integrifolius var. Fauriri

Erhard Roeder; K. Liu

Abstract A new water-soluble pyrrolizidine alkaloid quaternary salt, N -methyl- O 7 , O 9 -diangeloyl-1-hydroxyl platynecinium chloride, a new saturated pyrrolizidine alkaloid, O 7 -angeloylturneforcidine, a new saturated otonecine pyrrolizidine, 1,2-dihydrosenkirkine, a known alkaloid, O 7 -angeloylheliotridine and its N -oxide were isolated from Senecio integrifolius var. fauriri . The structures of the alkaloids and their stereochemistry have been elucidated by NMR analysis.


Phytochemistry | 1984

Pyrrolizidine alkaloids from Alkanna tinctoria

Erhard Roeder; Helmut Wiedenfeld; Rainer Schraut

Abstract Three pyrrolizidine alkaloids were isolated from Alkanna tinctoria and their structures analysed by spectroscopic methods. One of them is new and the name dihydroxytriangularine is proposed for it.


Phytochemical Analysis | 1997

Quantitative Photometric Determination of Senkirkine in Farfarae Folium

Jan-Pit Barko Bartkowski; Helmut Wiedenfeld; Erhard Roeder

A colour reaction for unsaturated pyrrolizidine alkaloids is made applicable for the first time to otonecine alkaloids and is used for the photometric determination of senkirkine in coltsfoot. The method allows the determination of 1 μg of alkaloid in 1 g of dried drug (i.e. 1 p.p.m.) and is therefore a useful alternative to the more exacting gas chromatographic determination.


Phytochemistry | 1990

Pyrrolizidine alkaloids from Lithospermum erythrorhizon

Erhard Roeder; B. Rengel

Abstract Three pyrrolizidine alkaloids were isolated from Lithospermum erythrorhizon and their structures analysed by spectroscopical methods. One of them is new and the name hydroxymyoscorpine is proposed for it.


Phytochemistry | 1985

Pyrrolizidine alkaloids from seeds of Crotalaria scassellatii

Helmut Wiedenfeld; Erhard Roeder; Edzard Anders

Abstract Three pyrrolizidine alkaloids were isolated from the seeds of Crotalaria scassellatii . Axillaridine and axillarine were the two major alkaloids whereas the third minor alkaloid was a new compound. Its structure was determined as desoxyaxillarine.


Phytochemistry | 1984

Pyrrolizidine alkaloids from Senecio cacaliaster

Erhard Roeder; Helmut Wiedenfeld; Ruth Britz-Kirstgen

Abstract Four pyrrolizidine alkaloids have been isolated from Senecio cacaliaster and their structures analysed by spectroscopic methods (IR, mass, 1 H, 13 CNMR). One of them is new and the name sencalenine (3) is proposed. Alkaloids O 7 -senecioylretronecine (1) and 7-senecioyl-9-sarracinylretronecine (2) have recently been identified elsewhere. The fourth is bulgarsenine (4) which was isolated from a Senecio species before.

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John A. Edgar

Commonwealth Scientific and Industrial Research Organisation

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