M
Matthew J. Rieser
Researcher at Purdue University
Publications - 15
Citations - 959
Matthew J. Rieser is an academic researcher from Purdue University. The author has contributed to research in topics: Annona muricata & Annonaceae. The author has an hindex of 11, co-authored 15 publications receiving 926 citations. Previous affiliations of Matthew J. Rieser include University of Minnesota.
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Journal ArticleDOI
Determination of Absolute Configuration of Stereogenic Carbinol Centers in Annonaceous Acetogenins by 1H- and 19F-NMR Analysis of Mosher Ester Derivatives
Matthew J. Rieser,Matthew J. Rieser,Yu Hua Hui,Yu Hua Hui,J. Kent Rupprecht,J. Kent Rupprecht,John F. Kozlowski,John F. Kozlowski,Karl V. Wood,Karl V. Wood,Jerry L. McLaughlin,Jerry L. McLaughlin,Paul R. Hanson,Zhiping Zhuang,Thomas R. Hoye +14 more
TL;DR: The absolute configuration of the stereogenic carbinol centers in nine annonaceous acetogenins has been determined by careful 1 H- and 19 F-NMR analysis of (S)- and (R)-Mosher ester [methoxy(trifluoromethyl)phenylacetate or MTPA] derivatives as mentioned in this paper.
Journal ArticleDOI
Annonaceous acetogenins: An updated review
TL;DR: The Annonaceous acetogenins as mentioned in this paper are a class of bioactive natural products whose antitumour, pesticidal and other bioactivities are due to inhibition of electron transport in mitochondria.
Journal ArticleDOI
Muricatacin: A simple biologically active acetogenin derivative from the seeds of annona muricata (annonaceae)
TL;DR: A biologically active constituent, bearing similarities to the annonacin group of Annonaceous acetogenins, has been isolated from the seeds of Annona muricata and the absolute configuration about the tetrahydrofuran ring of ann onacin is proposed.
Journal ArticleDOI
Five novel mono-tetrahydrofuran ring acetogenins from the seeds of Annona muricata.
TL;DR: Bioactivity-directed fractionation of the seeds of Annona muricata L. (Annonaceae) resulted in the isolation of five new compounds, three of which are among the first cis mono-tetrahydrofuran ring acetogenins to be reported.
Journal ArticleDOI
Muricatetrocins A and B and Gigantetrocin B: Three New Cytotoxic Monotetrahydrofuran-Ring Acetogenins from Annona muricata
Matthew J. Rieser,Xing-Ping Fang,Jon E. Anderson,Laura R. Miesbauer,David L. Smith,Jerry L. McLaughlin +5 more
TL;DR: In this article, the seeds of Annona muricata yielded three new Annonaceous acetogenins: muricatetrocin A (= (5S)-3-{(2R)-2-hydroxy-9-{ (2R, 5S)-tetrahydro-5-[(1S,4S,5S]-1,4,5-trihydroxyheptadecyl]furan-2-yl}nonyl}-5-methylfuran-2(5H)-one; 1), mur