Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Joan Mutanyatta-Comar"'
Publikováno v:
ACS Symposium Series ISBN: 9780841237483
ACS Symposium Series
ACS Symposium Series
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1bfdaa84fb2e17629eacdad772947715
https://doi.org/10.1021/bk-2019-1341.ch011
https://doi.org/10.1021/bk-2019-1341.ch011
Autor:
Tanya Gupta, Supaporn Kradtap Hartwell, Amy Flanagan Johnson, Ross Nord, Ryan T. Hayes, David W. Randall, Kirsten A. Casey, Lynn J. Tracey, Kristine E. Miller, Elizabeth A. Gabbard, Stacy I. Chamberlin, Lynetta M. Mier, Lori A. Bolyard, Brad M. Neal, Ann R. Cutler, David K. Styers-Barnett, Emily F. Kerr, Martin Samuels, Jose A. Zavala, Rajat Chadha, Diana M. Steele, Christian Ray, Jeffrey S. Moore, Susan M. King, Ninger Zhou, Christian Fischer, Fernando Rodriguez, Mark Warschauer, Susan M. Schelble, Chad L. Magee, Ryan A. Dohoney, Joan Mutanyatta-Comar, Suazette R. Mooring, Brian D. Gute, Jacob W. Wainman
Autor:
Joan Mutanyatta-Comar, Doris Feineis, Gerhard Bringmann, Stefan Rüdenauer, Raina Seupel, Andreas Irmer
The natural tetrahydroisoquinoline phylline (4) was synthesized in a specifically [1,1′-13C2]-labeled form, and fed to callus cultures of Triphyophyllum peltatum. Its incorporation into naphthylisoquinoline alkaloids, among them habropetaline A (8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55eb9c2f88a545ced232097445c12394
https://ora.ox.ac.uk/objects/uuid:a2cd57f0-1096-426c-b9b1-574fc5612eb6
https://ora.ox.ac.uk/objects/uuid:a2cd57f0-1096-426c-b9b1-574fc5612eb6
Joziknipholones A and B: The First Dimeric Phenylanthraquinones, from the Roots ofBulbine frutescens
Autor:
John M. Wanjohi, Martin G. Peter, Jacob O. Midiwo, Joan Mutanyatta-Comar, Matthias Heydenreich, Katja Maksimenka, Reto Brun, Gerhard Bringmann, Werner E.G. Müller, Abiy Yenesew
Publikováno v:
Chemistry - A European Journal. 14:1420-1429
From the roots of the African plant Bulbine frutescens (Asphodelaceae), two unprecedented novel dimeric phenylanthraquinones, named joziknipholones A and B, possessing axial and centrochirality, were isolated, together with six known compounds. Struc
Publikováno v:
Tetrahedron. 63:9810-9824
Triggered by a seemingly inconsistent twisting direction in the atroposelective ring cleavage reaction of biaryl lactones by using the ‘lactone concept’, the absolute axial configurations of the most important phenylanthraquinones, knipholone (1)
Autor:
Joan Mutanyatta-Comar, Marco Greb, Stefan Rüdenauer, Andreas Irmer, Torsten F Noll, Gerhard Bringmann
Publikováno v:
Tetrahedron. 63:1755-1761
Biosynthetic studies on naphthylisoquinoline alkaloids involving a specifically [1,1′-13C2]-labeled dihydroisoquinoline 7 are described. The synthesized precursor 7 was fed to callus cultures of Triphyophyllum peltatum and the isolated secondary me
Publikováno v:
ChemInform. 39
Covering: up to May 2008 This review gives the first comprehensive overview of the rapidly emerging young class of 4-phenylanthraquinones isolated from the three genera Bulbine, Bulbinella, and Kniphofia, all from the plant family Aphodelaceae: their
Publikováno v:
Natural product reports. 25(4)
Covering: up to May 2008 This review gives the first comprehensive overview of the rapidly emerging young class of 4-phenylanthraquinones isolated from the three genera Bulbine, Bulbinella, and Kniphofia, all from the plant family Aphodelaceae: their
Autor:
Matthias Heydenreich, Katja Maksimenka, Jacob O. Midiwo, Mueller Werner E G, Abiy Yenesew, Joan Mutanyatta-Comar, John M. Wanjohi, Martin G. Peter, Gerhard Bringmann, Reto Brun
Publikováno v:
ChemInform. 39
Publikováno v:
Natural Product Communications. 2:1934578X0700200
This review covers the phytochemical, biological properties, and synthesis of naturally occurring homoisoflavonoids. Homoisoflavonoids are a very important class of secondary metabolites whose numbers have grown from 20 in 1981 to 157 at the present